#lab cell strainer

[uberstrainerseo]

What Is PluriCell? Everything You Need to Know About This All-in-One Cell Culture and Filtration System

In laboratories that handle tissue digestion, live-cell assays, and organism tracking, combining cell separation and cell culture steps can save time and reduce contamination risks. That’s where PluriCell, a multi-well Lab Cell Strainer system, offers a game-changing solution. It allows filtration and culturing within the same plate setup—minimizing handling, maximizing throughput, and supporting high-precision assays.

Whether you're working with nematodes, single cells, or small multicellular organisms, PluriCell simplifies the workflow by integrating size-based filtration directly into multi-well plates. For labs looking to improve efficiency without compromising on accuracy, understanding how PluriCell works—and why it’s different from standard cell strainers—is the first step to adopting a better solution.

What Is PluriCell? A Quick Overview

PluriCell is a sample preparation and assay tool designed for researchers working with single-cell and multi-cellular organisms. The system includes nylon mesh-based strainers pre-fitted into standard well plate formats (6-, 12-, 24-, and 48-well). Each strainer plate fits snugly into corresponding well plates, allowing size-based cell separation and in-well culturing to occur simultaneously.

The mesh comes in multiple sizes—ranging from 5 µm to 500 µm—offering flexibility for diverse cell types or organisms. From isolating parasites to preparing single-cell suspensions for screening, PluriCell covers a wide range of applications while maintaining a compact footprint and simple setup.

Most importantly, PluriCell is not just a cell strainer—it’s a complete in-well assay platform that supports live tracking, treatment, and endpoint measurement of cultured samples.

How PluriCell Combines Filtration and Culture

Traditional workflows require multiple steps for size separation and cell plating. Samples are often strained through mesh filters, transferred into culture plates, and then moved again for drug testing or analysis. These transfers increase the risk of losing viable cells, introduce inconsistencies, and lengthen protocol times.

PluriCell changes that. It enables the particle separation process to occur directly in the same environment where the culture or assay will take place.

Key Benefits:

One step to filter and culture: No more transferring between mesh filters and plates.

Reduced sample loss: Cells or organisms are never handled more than necessary.

Higher reproducibility: Less manual handling leads to more consistent results.

Supports live assays: Migration, paralysis, and viability studies can be done without removing the sample.

Plate Format and Mesh Options

The PluriCell system is compatible with common lab equipment and comes in a range of configurations:

Multi-Well Plate Formats:

6-well

12-well

24-well

48-well

These options allow labs to scale up or down based on throughput needs, from small pilot studies to large screening assays.

Mesh Sizes Available:

Fine Meshes: 5, 10, 20, and 40 µm for single-cell filtration and smaller organisms.

Intermediate Meshes: 70 and 100 µm, ideal for cell clusters and small larvae.

Coarse Meshes: 200 and 500 µm for nematodes and larger multicellular samples.

This mesh variety allows labs to select exactly the right tool for their target sample. Instead of compromising by using an oversized or undersized filter, labs can match mesh size to assay requirements, enabling more accurate particle separation techniques.

Cascade Straining in a Multi-Well Format

One standout feature of PluriCell is how easily it enables cascade straining. Cascade straining refers to passing samples through a series of filters with decreasing pore sizes. This technique is especially helpful when dealing with tissues or samples containing a mix of particles, cell types, or organisms.

With PluriCell’s multi-well setup, each well can hold a strainer of a different mesh size. Researchers can load the sample once and allow gravity or light pipetting to filter the sample through wells in a defined sequence.

Example Workflow:

Start with a 500 µm mesh to remove large debris.

Next, use a 100 µm mesh for small tissue clusters or larger organisms.

Finish with a 40 µm mesh to isolate single cells or small larvae.

This setup provides fast and easy cell separation without repeated sample handling or multiple filter tools. More importantly, the entire cascade can happen within a single plate—saving time and preserving sterility.

Applications in Research and Screening

PluriCell isn’t just about convenience. It also enables entirely new types of experiments. Because cells or organisms remain in the well after filtration, they can be directly exposed to drugs, dyes, or environmental changes.

Common Use Cases:

Parasite migration assays

Viability and toxicity testing

Stem cell and primary cell culture

High-throughput screening (HTS)

Live imaging of multicellular organisms

Labs that handle fragile specimens like C. elegans, planarians, or patient-derived cell types benefit most. The system minimizes stress on the sample while maintaining clarity and access for measurement tools.

Why Mesh Integrity and Build Quality Matter

For labs used to standard lab cell strainers, PluriCell may appear similar—but its mesh quality sets it apart.

Uniform nylon mesh ensures consistent flow rates and pore sizing.

No deformation or mesh slippage, even after repeated handling.

Sterile and single-use to maintain culture conditions and reduce contamination risk.

PluriCell vs. Traditional Culture + Filtration Setups

When comparing PluriCell to standard lab filtration and culture workflows, several distinct advantages stand out:

Filtration Method Traditional workflows rely on external tools like syringe filters or cap strainers for filtration, which must then be manually transferred to culture plates. PluriCell integrates filtration directly into the well plate, eliminating the need for separate filtering devices.

Sample Handling and Transfers Conventional methods involve multiple handling steps, increasing time and risk of error. With PluriCell, filtration and culture occur in the same well, streamlining the process into a single step.

Contamination Risk Each manual transfer in traditional workflows increases the likelihood of introducing contaminants. PluriCell reduces this risk with its sealed design and sterile, ready-to-use format.

Assay Readiness In standard setups, separate tools are required to move from filtration to culturing or assays. PluriCell is fully integrated—after filtration, samples remain in place for immediate treatment, observation, or analysis.

Scalability and Throughput Traditional methods require manual adjustments and more consumables to scale up. PluriCell supports high-throughput formats with 6-, 12-, 24-, and 48-well options, making it easy to expand workflows without adding complexity.

How PluriCell Saves Time in Lab Workflows

Time is a valuable resource in any lab. The fewer the steps, the less room there is for error, delays, or sample loss. PluriCell’s design reflects an understanding of this.

Here’s how it streamlines your process:

Quick setup: No assembling mesh tools or transferring between formats.

Fewer consumables: Plates, filters, and supports are combined in one product.

Immediate use after filtration: Cells or organisms are already in place for assays or culture.

This speed and simplicity are what make PluriCell a practical upgrade from standalone lab cell strainer tools.

Conclusion

PluriCell offers more than filtration—it transforms how researchers approach cell preparation and culture. By combining mesh-based separation with multi-well assay formats, it simplifies complex protocols and supports more reliable data generation.

Its compatibility with various mesh sizes, plate formats, and cell types makes it a versatile tool for modern labs. Whether you're filtering single cells, tracking nematode migration, or running live-cell drug response assays, PluriCell delivers consistent, clean, and assay-ready results.

For labs serious about improving throughput and reducing variability, Lab Cell Strainer like PluriCell represent a powerful upgrade over traditional tools. Explore the full range of PluriCell systems today to streamline your workflow and make every assay count.

[uberstrainer]

Advancing Cell Separation: Comprehensive Solutions for Leukocyte Enrichment and PBMC Isolation

This article explores the advanced cell separation technologies, highlighting the ready-to-use density gradient media for efficient isolation and enrichment of leukocytes and PBMCs from blood samples, which are crucial for immunological and clinical research.

Cell separation technology is a cornerstone of immunological and clinical research, enabling scientists to isolate specific cell populations from complex biological samples. pluriSelect offers a range of ready-to-use density gradient media designed for the precise and efficient isolation of various blood cell populations. These media facilitate single-step density gradient centrifugation, providing high yields and purity for downstream applications such as antibody cell separation, particle filtration, and cell culture.

Density Gradient Centrifugation: A Key Technique

Density gradient centrifugation is an essential method in cell separation technology. This technique separates cells based on their density by layering blood or other sample materials over a density gradient medium and subjecting them to centrifugal force. The cells stratify into distinct layers, allowing researchers to extract target cell populations with high purity.

PBMC-Spin®: Precision in PBMC Isolation

PBMC-Spin® is a density gradient medium with a density of 1.077 g/ml, optimized for isolating peripheral blood mononuclear cells (PBMCs), including lymphocytes and monocytes, from fresh samples. This ready-to-use medium ensures efficient separation within 12 hours of sample collection. PBMC-Spin® is ideal for obtaining PBMCs for various research applications, including immunological studies and cell culture.

Leuko Spin: Enriching All Leukocytes

Leuko Spin is another innovative product designed for the enrichment of all leukocytes from fresh human peripheral blood or buffy coat. This sterile, ready-to-use medium allows for the isolation of mononuclear and polymorphonuclear cells through single-step density gradient centrifugation. When combined with PBMC-Spin® in a double gradient centrifugation process, Leuko Spin enables the simultaneous isolation and separation of granulocytes and PBMCs, providing high yield and purity. The enriched cells are suitable for a range of downstream applications, such as magnetic activated cell sorting (MACS) and stem cell research.

PBMC24+ Spin: Effective Isolation from Older Samples

For researchers working with blood samples older than 12 to 24 hours, PBMC24+ Spin is the recommended choice. This medium minimizes contamination with granulocytes and erythrocytes that typically increase over time. PBMC24+ Spin ensures high purity and yield, even 24 hours post-sampling, making it an excellent solution for isolating PBMCs from older samples. These cells can be used in various downstream applications, including MACS and stem cell research.

PLT Spin: Optimized for Platelets

PLT Spin Medium is specifically formulated for the isolation of platelets from fresh human peripheral blood. This ready-to-use, sterile medium facilitates high-yield platelet separation through single-step centrifugation, making it invaluable for research applications requiring pure platelet populations.

Monocyte Spin: Gentle Enrichment for Monocytes

Monocyte Spin Medium offers a gentle alternative to bead-mediated monocyte enrichment methods. This ready-to-use, sterile medium is designed for the isolation of monocytes from fresh peripheral blood or buffy coat, achieving purity levels of 60-80%, depending on the sample. Monocyte Spin is particularly suitable for downstream applications such as cell culture and differentiation, where maintaining cell integrity is crucial.

Customizable Density Solutions: HDSM and DDM Spin Medium Set

For researchers requiring tailored density gradients, pluriSelect provides the High Density Spin Medium (HDSM) and Density Diluent Medium (DDM) set. This set allows for the preparation of customized density working solutions for the enrichment of cells, bacteria, and other particles. By mixing HDSM with DDM, users can achieve densities between 1.0 and 1.1 g/ml, accommodating a wide range of sample types and isolation requirements.

Applications and Benefits

The enriched cell populations obtained using pluriSelect’s density gradient media are suitable for various applications, including:

Immunological Research: Isolating specific immune cell populations to study immune responses.

Stem Cell Research: Enriching stem cells for differentiation and proliferation studies.

MACS: Using magnetic beads to further purify specific cell types.

Cell Culture: Culturing isolated cells for in vitro studies.

In conclusion, pluriSelect’s comprehensive range of density gradient media supports efficient and precise cell separation, facilitating advancements in immunological and clinical research. These products enable researchers to achieve high yields and purity in their cell separation procedures, contributing to the development of targeted therapies and a deeper understanding of cellular biology.

[oilpurifiermachines]

The Ultimate Guide to Oil Filtration: Maximizing Equipment Life and Performance

Dirty oil is a silent killer. Unseen contaminants smaller than a human hair—particles, water, acids—wreak havoc on hydraulic systems, engines, and turbines. Studies show that just one overheating event can slash hydraulic component lifespan by 66% . In industrial settings, contaminated oil causes up to 80% of hydraulic failures. Yet most operations remain unaware until it’s too late: seized pumps, clogged valves, costly unplanned downtime.

Oil filtration isn’t just maintenance—it’s a strategic investment. Modern solutions can boost oil cleanliness four times higher than standard synthetics, extending critical component life by 60% . This guide dives deep into the science, technology, and best practices transforming oil from a liability into an asset.

I. Why Oil Filtration Isn’t Optional

Oil degrades predictably, but its consequences are catastrophic:

Particle Warfare: ISO 4406 classifies contaminants by size (4µm, 6µm, 14µm). Particles as small as 5µm—half the width of a human red blood cell—act like abrasive sandpaper in bearings and gears. A single gram of dust entering a system can generate millions of destructive particles .

Water, the Invisible Enemy: At just 0.1% water content (1000 ppm), bearing life plummets by 50%. Water induces oxidation, forms sludge, and promotes microbial growth (“diesel bugs”) that clogs filters .

Thermal Runaway: Overheated oil (>180°C in fryers, >60°C in hydraulics) cracks molecular chains. The result? Viscosity changes, varnish deposits, and accelerated acid formation.

The Solution Spectrum:

Straining (25-30µm): Removes chunks only. Useless against fine killers.

Mechanical Filtration (1-10µm): Captures damaging particles but requires pressure.

Full Purification: Combines filtration, dehydration (vacuum or coalescing), and sometimes chemical treatment for total fluid rehabilitation .

II. Inside the Filtration Revolution: Technologies Decoded

A. The Mechanics of Cleanliness

Vacuum Towers: Not all water removal is equal. Basic settling tanks leave emulsified water. Vacuum chambers (at -0.07 MPa) boil off water at lower temperatures (45-70°C), preserving oil integrity. This is critical for moisture-sensitive turbine oils .

Multi-Stage Filtration:

Pre-Filters (50-100µm): Catch weld slag or metal chips. Easily cleanable stainless mesh.

Primary Filters (10-25µm): Trap wear-inducing silt.

Final Polishing (1-5µm): Glass fiber or synthetic media capture residual fines.

Pro Tip: Always place filters in series—coarse to fine. Skipping stages clogs $300 filter cartridges with debris a $30 strainer could catch .

B. Cutting-Edge Media: Beyond Basic Mesh

Its layered micro-glass fibers lock particles during flow surges—critical in variable-rate hydraulics. Lab tests show two ISO code improvements over synthetics—meaning 60% longer pump life .

Depth Loading vs. Surface Capture: Traditional cellulose (paper) filters trap contaminants on the surface, clogging fast. Depth media like borosilicate microfibers embed particles throughout the matrix, tripling dirt-holding capacity .

C. Smart Filtration: The IoT Edge

Systems like DISA’s Optimal Oil Filtration (OOF) module monitor in real-time:

Particle counts (ISO 4406/NAS 1638)

Water concentration (ppm)

Temperature anomalies

Dielectric strength (indicating oxidation)

When values degrade, it triggers auto-remediation: activating offline filters or alerting technicians before damage occurs .

III. Operating for Zero Failures: A Step-by-Step Playbook

A. Startup Protocol: Safety First

Grounding Check: Static sparks in oil vapor are explosive. Verify earth connections .

Dry Run Prevention: Seal all connections. Air ingress creates foam, crippling vacuum efficiency.

Flow Direction: Reverse flow ruptures filters. Confirm arrows on housing match piping .

B. The Golden Rules During Operation

Pressure Tells All: Normal range: 0.05–0.3 MPa. If >0.4 MPa, immediately shut down. This signals a blinded filter or blocked line. Forcing oil past ruptures media, flooding systems with debris .

Temperature Sweet Spots:

Hydraulic oils: 45–55°C (↑ viscosity index, ↓ water)

Cooking oils: ≤180°C (above this, carcinogenic compounds form)

Vacuum Integrity: If moisture separation drops, check for:

Seal leaks (hissing sounds)

Pump oil emulsification (change if milky)

C. Strategic Shutdown & Storage

Cooldown Phase: Stop heaters 5+ minutes before pumps. Residual heat prevents wax/carbon formation .

System Drainage: Stagnant oil breeds bacteria. Open all drain plugs—especially in humid climates.

Filter Preservation: Remove cartridges, bag them, label with µ-rating and date. Left installed, they leach contaminants back into clean oil.

IV. Maintenance: Predicting the Unpredictable

A. Filter Change Triggers

Indicator Action Required Cost of Delay ΔP > 0.3 MPa Replace element NOW Housing rupture ($5k+) ISO Code ↑ by 2 classes Check seals + media integrity Bearing spalling ($25k) Water > 500 ppm Run vacuum cycle + test additive Corroded servo valves ($12k)

B. Contamination Forensics

Shiny Metal Flakes? Pump or gear wear. Send oil for spectroscopy.

Black Sludge? Overheating. Check cooler operation.

White Emulsion? Water ingress. Inspect seals/coolers .

C. Proactive Lifespan Extenders

Additive Replenishment: ZDDP anti-wear agents deplete. Titration kits reveal needs.

Flush Before Fill: New oil isn’t clean (ISO 21/19/16 average). Filter during transfer.

Breather Upgrades: Desiccant caps prevent humid-air ingress—$50 fix for 10x cleaner oil.

V. Industry-Specific Solutions

A. Hydraulics: The Pressure Is Real

Why it Matters: Servo valves tolerate ≤ 5µm particles. Contamination causes erratic motion, drift.

Toolkit: Install duplex filters with valved switchover. Clean one side while operating the other—zero downtime .

B. Food Production: Beyond Clarity

Crisis: Straining fryer oil at 30µm leaves fines that burn into carcinogens (acrylamide).

Fix: 1–5µm absolute filters + activated clay absorbers remove polar compounds. Result: 30% longer oil life, lighter-colored food .

C. Wind Turbines: High Stakes, Hard Access

Challenge: Remote gearboxes fail from moisture-induced pitting.

Smart Fix: Permanent offline filtration loops with real-time moisture sensors. Data triggers maintenance before ice or storms prevent access.

VI. The Future Is Cleaner, Smarter, Autonomous

Self-Healing Media: Nano-coated fibers that release enzymes to digest sludge (lab-tested by ExxonMobil).

Carbon Capture Integration: New systems like Donaldson Reclaim capture vented VOCs, converting them to inert compounds.

Predictive AI: Algorithms correlating pressure spikes with impending pump failures (accuracy: 94% in trials).

VII. Choosing Your Champion: A Buyer’s Checklist

Ask these questions before selecting a system:

What’s Your Baseline? Get an ISO particle count—don’t guess!

Flow Flexibility

Fixed-rate? Gear pumps suffice.

Variable hydraulics? Prioritize surge-resistant media like Alpha-Web® .

Disposal Reality

On-site incineration? Standard filters work.

Landfill restricted? Opt for biodegradable media (soy/plant-based).

Total Cost of Ownership

Cheap filters = frequent changes.

Calculate: (Element Cost × Annual Changes) + Labor + Disposal Fees.

Final Thought: Filtration isn’t about removing dirt—it’s about preserving precision. Every micron captured extends the dance of finely machined components. With oil cleanliness as your compass, unplanned downtime becomes optional, not inevitable.

Got a filtration horror story or victory? Share below—let’s dissect the lessons.

[deniselabmate]

ABS Cell Strainer

An ABS Cell Strainer is a laboratory tool for filtering cells or particles from solutions. Made of durable ABS plastic, it features a mesh filter membrane for precise filtration. Ideal for cell culture and sample preparation in research and clinical labs.

[digitalsomnath]

How Pluristrainer Can Help In Obtaining High-Quality Real Single-Cell Suspensions?

Cell strainers are one of the most essential tools in determining the success of an experiment. Read on to learn the benefits of using PluriStrainer.

When it comes to cell sorting by flow cytometry, more attention to sample preparation is often required than when only preparing samples for analysis. When sorting, the goal is to not only separate some sample fraction in a timely manner so that the sorted output is a pure viable fraction, but also for the sorted cells to be functionally capable, to expand well in culture, or to perform well in some other subsequent assay.

 Another requirement for good cell sorting is a proper single-cell suspension, which ensures a desirable sample behavior inflow and allows for good doublet discrimination with minimal conflict aborts. How can you get the best sample behavior and performance?

 PluriStrainer

PluriStrainer, one of the best Lab Cell Strainers, is a sterile sieving device for obtaining true single-cell suspensions or removing cell aggregates. Its unique design allows for better ventilation to prevent clogging, and it can be used in conjunction with a Connector Ring (41-50000-03) to use low pressure to support filtration. On the following page, you'll find more applications.

 When should you use Pluristariner?

·         After enzymatic digestion of mammary tissue and organoids, the real single-cell suspension is obtained.

·         Dissociation of primary tissue on a physical level

·         Single-cell suspensions of blood cells from bone marrow, pancreas, thymus, lymph nodes, and other sources are prepared.

·         Flow cytometry preparation of a real single-cell suspension Filtration with gauze is a faster and easier option.

·         Incubation of cells/cytokines for a short period of time (in combination with pluriBead® and Connector Ring)

·         Liquids that are complex and viscous, such as fat tissue, are sieved (in combination with a low-pressure syringe and a Connector Ring).

 Applications

 PluriStrainer

Plug the pluriStrainer onto a 50 mL tube.

On top of that, place your sample material. Only a small portion of your sample material will be processed. You can force low pressure to support the straining of rough sample material while pulling the piston by adding a syringe to the Connector Ring.

 Stacked pluriStrainer

PluriStrainers, the best Lab Cell Strainers, comes with different mesh sizes that can be stacked to strain different cell sizes at the same time.

 Reversed pluriStrainer

Remove the pluriStrainer, turn it upside down onto another 50 ml tube, and flush the sample back into the pluriStrainer to obtain the larger fraction.

 PluriStrainer with Connector Ring

It allows you to control the rate of flow by opening or closing the Luer-Lock, which is useful for physical tissue dissociation (brain, spleen, etc.).

When you open the Luer-Lock, the sample material will flow through.

 PluriStrainer with Funnel

On the pluriStrai-ner, insert a funnel (42-50000-03).

On top of that, you can add up to 24 mL of sample material.

 Connector Ring, PluriStrainer®, and Syringe

You can force low pressure to assist the straining of rough sample material while pulling the piston by attaching a syringe to the Connector Ring,

 Specifications

·         Mesh Size: 1 - 500 μm

·         Mesh Material: PET

·         Mesh Type: Woven

·         Housing Material: LD-PE (Low-Density Polyethylen)

·         Sterility: Gamma Ray Sterilized

 Key features

·         Sieving with mesh sizes ranging from 1 to 500 m is a simple process.

·         To get the larger fraction, reverse the process.

·         Multiple target sizes can be stacked.

·         Larger sample volumes require a funnel.

·         Connector Ring for Flow Control

·         Low pressure is used to aid sieving.

 Do you want to find the best cell strainer for your research? Visit our website and check the high-quality products that you need for cell or particle separation.

[as-unhuman-as-can-be]

Some shit heard by AP students

“Can I bring my fish in for show and tell”

“I had to wikihow how to make a paper airplane”

“Hitler always had my vote”

“Well bath bombs are a big thing now and guess who wants to get baptized”

“You already tried to deepthroat your phone!”

“You look like cotton candy and not in the good way”

“Spain... influenza...Spanish Inquisition... hehe“

“They were a slippery people they were”

“Every time you complain about this lab a kitten hangs itself in a tree”

“Do you drain your pasta with your hands like a normal person or with a strainer like a Democrat?”

“What’s Richards last name?” “Nixon?”

“It’s hard to be an African American woman in this country when you’re white” (he was also a male)

“I’ll just become god”

“You have NOT seen her in volley ball. Flexible dick energy EVERYWHERE”

“My goal is to uhhhhh... study math”

“If gas gets to expensive, catch me fermenting”

“Oh shoot I actually had to use my last two brain cells”

“The Notre Dame chapel could survive the freaking French Revolution but NOT 2019”

“Grange fair is just Coachella for Hicks”

“My sleep paralysis demon is the Chick-fil-A ordering menu”

“You mean you don’t have a gun wall?”

“We love unneeded sex”

“1¢ does not equal $500”

“I’m just trying to get good at sonic”

“I’ve heard this terminology... tiktok... what is this?”

“Under the bag of ice there’s some loose leaf ice”

[allaboutlpr]

You Now Have Skin in the Game

LPR affects various sites in the larynx and the hypopharynx. The latter is the part of the throat that is beside and behind the larynx. It is the entrance to the esophagus. Because of this, it would be advantageous to have a research system that could distinguish among the  effects of reflux exposure on the tissues in different sites. This system could also interpret the therapeutic effectiveness of various treatments at the cellular level. The article summarized below describes the work of researchers in China who successfully isolated tissues from vulnerable areas and grew them in the lab.

The tissue layer that lines the throat and larynx is the mucosa. The outer surface of cells is the epithelium. The investigators sampled various sites within the laryngopharynx, taking specimens of the mucosa. The tissue was treated with enymes, then passed through a strainer and suspended in a growth medium.

The cells grew and divided, and the cultures attained a density of 94.9% epithelial cells. These cells could be transferred to fresh medium and they continued to grow.

This above description comes under the category of cell culture. Successful culturing (growth) of cells, (whether animal or plant), requires finding the proper nutrients and temperature to stimulate growth. This can be a long and complicated process. If successful, as in this case, this allows researchers to analyze down to the cellular level the effects of refluxed materials on specific areas of the throat. They can also measure the effects of potential pharmceuticals on those stressed cells. This kind of research allows investigations that would be difficult or impossible with living human subjects.

Optimized Generation of Primary Human Epithelial Cells from Larynx and Hypopharynx: A Site-Specific Epithelial Model for Reflux Research. Cell Transplantation. 2019 March 27

[mantashaasposts]

The Best Cell Strainers For Preparing Flow Cytometry Samples

Do you require cell strainers for the preparation of flow cytometry samples? Let’s find out the details of the best cell strainers.

It is extremely important to properly prepare the sample in order to achieve a smooth cell flow. The type of cells to be examined, as well as any other potential impediments to the flow, must be taken into account.

Running your sample through the best Lab Cell Strainers, which is essentially a piece of mesh with a specific porosity size to create a single-cell suspension, is a common part of proper preparation.

Cell Strainers

Cell strainers are used to isolate primary cells from test tubes or conical tubes in order to obtain single-cell suspensions. They are typically color-coded to assist you in determining which cell strainers to use for different tube sizes. They come in both non-sterile and sterile varieties. Cell strainers are made of nylon mesh with pores that are evenly spaced.

How Do The Cell Strainers Work?

Cell strainers remove debris or clumps from samples, allowing cells to be isolated for further testing. The cell strainers fit on the tops of various size sample tubes to help create a tight fit, so the material must pass through the strainer. 

Only certain materials can pass through the mesh, which is made up of different sizes. It allows for the separation of materials based on size, allowing for the isolation of a specific material from the rest of the sample.

Use Our Cell Strainers For:

Single-cell suspensions of blood cells are prepared from bone marrow, pancreas, thymus, and other sources. 

Dissociation of tissue for single-cell suspension and isolation 

Filtered and isolated primary and cell culture cells 

Flow Cytometry Sample Preparation 

How Our Range Of All-Star Strainer Can Help?

Pluriselect has a large selection of best Lab Cell Strainers to meet almost any need. You can select the ideal device for your sample preparation in meh sizes ranging from 1 m to 1000 m, PET or nylon fibers, sterile or non-sterile, small volumes up to 800 L or in-line-strainer, back-flush capability or not. The following are examples of straining/filtration devices:

PluriStrainer

Available in 15 mesh sizes

Fits in 50 ml tubes

Low pressure compatible

Stackable as cascade

Centrifugable with Connector Ring

Sterile, single-packed

ÜberStrainer

Available in 15 mesh sizes

Fits in 2, 15, 1.5, and 50 ml tubes

Low pressure compatible

Process unlimited amount of liquid

Centrifugable

Sterile, single-packed

PluriStrainer Mini

Available in 6 mesh sizes

Fits tubes ranging in size from 1.5 mL to 15 mL

Fills the gap for small sample volumes

Autoclavable

Centrifugable

Sterile, bulk-packed

Syringe Strainer

Available in 15 mesh sizes

Sterile and non-sterile varieties

Membrane Strainer

The exclusion limit for pore size is well-defined (available with 1, 3, 5, and 8 m pores).

Non-hygroscopic membrane

Low non-specific protein binding

Biologically inert, non-cytotoxic

Excellent chemical and temperature resistance

Steel Basket-Strainer

Fits in a 50 ml standard tube

Excellent mechanical stability of SS 316 steel

Perfect to extract liquids from a porous material

Reusable

Re-Strainer (In-Line-Strainer)

Available in 15 mesh sizes

6 ml recovery reservoir

Two femaleluer-lock-ports

Housing material is LD-PE (Low-Density Polyethylene)

Withstand pressure up to 3.5 kg/cm2

Are you looking for the best cell strainer for your research? To order high-quality cell or particle separation products, please visit our website.

[histologyapology]

Quiz Review #1: Water Quality

hhhhhhh i really don’t want to study tonight but this is a fairly interesting topic so I figured I’d try to bribe myself into some review by posting about it here. alright leggo. giant wall of text under the cut, strap in lads. 

Water Quality as it relates to histology is probably an overlooked topic in many labs. Many labs use tap water as a bluing reagent, and so the logic may be that if it’s good enough in that context then it must be fine for other steps in process, such as for water baths and rinsing steps in the H&E strainers. This isn’t the case; the ideal lab will have a water purification system that allows for water that goes through several layers of deionization, filtration and sterilization before it ever comes out of the spigot. But that’s getting ahead of things; let’s talk about why tap water isn’t usually a good idea for use in the histological setting:

Why is tap water bad? Five main Reasons:

 Tap water contains inorganic ions, which can negatively effect the quality of a whole bunch of special stains. Silver stains in particular are very vulnerable to inorganic ion contamination; it is common practice at my school to make students do a Gomori Methenamine Silver stain with tap water and a second with DI, just to demonstrate the difference the contrast and background staining issues. 

Tap water contains organic contaminants, such as those created by the breakdown of plants and algae. Bacteria and fungi find these substances extremely snack-able, which can lead to some false positives on bug stains. We actually had an issue with this in the lab at my previous rotation; the milipore guys wouldn’t tell us exactly what happened but going by the weird fish smell and the MANY  false positive bug stains from that week, we think it was an algal bloom/dieoff that fueled a giant bacteria party in the DI system! Fun times!                                        Another source of organic contaminants is the breakdown of plastic shipping materials and plumbing pipes, such as the polymers that leach out of PVC and water carboys. These are usually indicated by a harsh ‘chemical-y’ smell.

 Certain areas of the country may have issues with particulate and colloid pollution; most of the large particles (sand, rocks, plant bits) should be filtered from tap water by waste management, but certain substances such as calcium carbonate (aka limescale) are hard to get rid of and may cause crusty deposits on machinery and artifacts on slides.

Tap water can contain bacteria and their by-products, which is a big issue if you’re running any number of bug stains or histochemical enzyme tests. The bacteria themselves can give you a false positive on things like Grams, Gomori and Warthin-Starrys, and those bacteria contain can also cause degrade endogenous nucleic acids and screw up F/ISH testing.  

The last and probably rarest class of tap water pollutants is Gases and Fumes,including things like carbon dioxide, nitrogen, and fumes from acids and volatile solvents used in the lab. Carbon dioxide in particular can be an issue, because too much CO2 in water will cause it to acidify, which could mess with everything from basic H&E staining to tissue morphology. Xylene and alcohol evaporate very quickly; a lab with many open containers and/or poor ventilation may have areas where fumes ‘collect’ and these can sometimes condense onto an open water bath (tho can i just say? If your lab has open processors/open vats of xylene just sitting around??? get out of there, you’re going to get sick. rat out your management to OSHA. love yourself. jeeze). 

Alright so now you know why tap water is garbage, now let’s talk about how to measure the degree and severity of how garbage it might be. 

Measuring contamination:

Resistivity: a measurement of how strongly the water opposes an electical current moving through it. Remember genchem? yeah it sucked, but remember when you did that experiment where you put different salts into water and then recorded how easy or hard it was for an electric current to get through said water? It’s like that, but the inverse; resistivity is the inverse of conductivity. Pure distilled water does not conduct electricity well; it has a high resistivity. If your water has a bunch of inorganic contaminants in it, it will have a low resistivity, it’s going to conduct electricity very well, and the College of American Pathologists will yell at you and make you fix it or your lab will lose accreditation. Resistivity is measured using certified and calibrated meter. Details about the calibration of the meter and the periodic resistivity testing you do on your lab’s DI system should be recorded and presented to CAP when they come a-knockin’ at inspection time. 

Colony Forming Units: this is a measure of bacterial contamination where you plate some of your DI water onto some agar and see what grows. Make the nerds down in Micro do it so you don’t contaminate the plate with the sleeve of your scrubs and give yourself a heart attack. This is another measurement of water quality that CAP’s going to want to see during inspection, so keep good records. 

Alright so now we know what garbage is in tap water, we know how to measure that there garbage, now let’s figure out how to make some water that isn’t terrible, some nice pure delicious Science Water ® :

Purifying water: Seven ways

Distillation: Mankind’s been doing this one for thousands of years, tho usually it’s for getting drunk. The idea is to boil water and collect the steam that comes off. This will get rid of larger particulate pollution but may not get rid of some chemical pollution, so it’s best paired with another method. 

Reverse osmosis: ‘RO’ involves forcing contaminated water through a very fine membrane under enormous pressure. RO systems are expensive and making large quantities of water using RO can be time consuming, but the water quality they produce is generally worth it. 

Ion exchange: ion exchange involves two beds of resin, one positively charged and the other negatively charged. Contaminated water cycles through these beds, and any ionic contaminants are extracted from the water. The water itself dissociates into H+ and OH- ions, which can then be re-constituted to make pure water. 

electrodionization (EDI): EDI is a combination of Ion exchange and electrodialysis. The physics of how it works is a little complicated but there’s a nice video about it by Siemen’s here if you’re interested. The important thing to remember is that it is constantly regenerating the resins it uses in the ion exchange step, which makes it attractive to labs who don’t want to do a lot of maintenance (it is still recommended that you replace the ion beads periodically for quality control reasons; everything has a shelf life, you don’t want to push it). 

activated carbon: another classic. Carbon tends to be very porous, so if you let gravity pull water down through a thick layer of it, most larger particulates will get caught in these pores. This is neither a specific nor very powerful form of filtration, however, and is best paired with other methods. 

UV sanitation: A UV light is used to kill any aquatic life forms that may be in the water. Fishkeepers may be familiar with this method, it’s good for cutting down on algal blooms. 

Fine Filtration: a variety of filters can be used to reduce the amount of particulate pollution in water. they are split into two main categories: microporous and ultrafiltration. Microporous filters are basically large mats of fibrous material that physically trap particles while letting water flow through. Ultrafiltration membranes work at the molecular level, separating molecules based on size. Filtration with the method is extremely slow, so most labs opt to only use ultrafiltration for cell culture and molecular techniques. 

So there’s an important question outside of all the different filtration choices, and that is: How pure do you *need* your water do be? How much of it do you anticipate your lab needing? How fast do you need it to be able to replenish? Most labs will decide to choose some combination of these methods in order to best meet their needs and deal with the contaminants presented by their local water sources. The lab for my current rotation uses a combination of RO, EDI and UV, and circulates/re-filters unused DI several times each hour to avoid stagnation. We also have a number of rules about decontaminating pitchers, carboys and water lines within our stainers. We are strongly encouraged to use clear glass containers whenever possible even tho we all wear gloves all the time so we drop beakers all over the place ive only been there two weeks and its almost happened to me twice now

There are several classifications of water set by the Clinical Laboratory Standards Institute with varying degrees of purity for use in the laboratory setting:

Clinical laboratory reagent water (CLRW): In my lab, this is what comes out of the DI tap. It’s whats called for in most stain recipes and is what we put in flotation baths. 

Special reagent water: we use this for reconstituting antibodies and the F/ISH team uses it for PCR. It comes from the milipore machine in the genetics ward because they need it more often and apparently the machines are very expensive so we only get one per department. 

instrument water: It won’t clog your stainer lines but it’s not good enough for your flotation bath. 

‘water supplied by instrument manufacturer’: I’m told no one does this any more. apparently once upon a time lab machine companies would send you big ol boxes of water in the mail to use exclusively on their machines, but then no one was checking to see how chemically stable the packaging was and there were issues with polymer contamination; this was very much before my time so i don’t have a lot of details. 

Commercially bottled purified water: another method that’s no longer popular since apparently most  bottled water is just tap water from someplace else and you’d still have to plate for CFU’s, test for resistivity etc

autoclave and wash water: tap water. Remember though, you should always give your glassware a final rinse with DI before hanging it up to dry toget rid of anything funky in the tap water. 

So yeah that’s how you make and monitor some sweet sweet Science Water, aka the Good Stuff. My next unit is on PAS/PASD, that’ll probably be up next sunday-ish. Til then,

-Reby

[emeraldinthesky]

STRANGE TRAILS - Chapter 3 - Logsense

Cooper paused at room 321. He glared at the peculiar number, a boyish enthusiasm still flickering in his limbs and especially fingertips. The corners of his mouth remained turned up, and it seemed impossible for them to frown. He stepped closer to the door. He couldn't wait to tell her all about the Bookhouse Boys.

Yes, the town's secret organization was a secret; however, the peculiar thing with men is that the woman closest to them was their confidant. Be it mother, partner, or sister - they shared everything with her, and for agent Cooper, that role was still fulfilled by Victoria. And yet, as he was about to knock on the door, the beaming smile washed away from his face. He couldn't get himself to wake her, however gladly she would have listened to his stories, not after seeing her so tired. Not after what happened between them.

While Cooper further investigated the case late into the night, Vicky was catching up on sleep. That is, if you call tossing around in bed from nightmares, sleeping. She was never a good sleeper. Oftentimes, she went out for a cigarette in the middle of the night to stare at the current shape of the moon from Dale's balcony. She was familiar with all its phases: gibbous, waning, waxing… Of course, it was the most interesting to observe in its full glory, but Victoria found it much more soothing when all was covered in the heavy cloak of darkness. Especially when Cooper rolled out of bed to embrace her from behind, only to fall back asleep on her shoulder moments later.

…as the midnight of a moonless night…

She was used to nightmares, too, so much in fact, that she simply referred to them as dreams by this point. Rotting flesh pulsating alive again, beating hearts being opened with a scalpel, bodies moving with eery naturality as they were carved with medical devices like ancient stones and as you got to a certain organ, they spoke:

'Nurse, there's a twitching in my left thigh…'

She was called a nurse many times during her residency and the people on the surgery tables were rarely any different or more alive than the DBs she was investigating in her recent years. Both were flesh, still infused with the illusion of the self, but regardless… Flesh. Maybe it was this connection that made her more aware of the fine line that separated life and death.

This time it was the blonde girl, Laura Palmer, speaking to her, while Albert kept drilling her head into a strainer. 'Birdzzzzz… birdzzzz…' She repeated, syncing up with the instrument's buzzing, like a broken record, until her brain leaked from the holes like playdoh. Her eyes, her striking blue eyes remained locked on Vicky. Laura's thoughts evaporated from her cells. The cloud of memories engulfed the three of them as faint whispers, growing louder and louder, circling around the girl like a tornado, the wind picking up the drill from Albert's hand, carrying it away with Toto, yet the tool kept buzzing on and on and…

Vicky woke to the beeping of her alarm. She silenced it and her eyes darted wide open. She wasted no time, rushed to the small table by the window, and took the folder of evidence on it. A sudden blackness came over her. She threw the opened folder back to the table to grab the side of the furniture for stability. She saw nothing even though she was forcing her eyes to stay open. 'Breathe deep,' she thought to herself while taking a long inhale. The feeling was not unfamiliar to her. It was a frequent occurrence during her ambulance shifts whenever they had to storm out to a case. As she regained her consciousness, she fumbled around for a specific photograph she was inspecting right before falling asleep: the strange scars on Laura Palmer's shoulders. When she found it she immediately dialed: 'Albert!' She exclaimed when she heard the phone being picked up. 'It's bird pecks on her shoulders.' 'On the Palmer girl?' Her supervisor asked without missing a beat. The woman could hear a similar shuffling at the end of the other line, and after a short pause, Albert agreed. 'You're right. I'll have McCoy run it through the database. Did your date with Coop go well?' 'Yeah,' She replied absent-mindedly, failing to pick up on the mocking tone of the man's voice. 'When does the equipment arrive here?' 'Should be about an hour,' Came the reply. 'Good job, Vicky.'

~Invitation to love~ 'Don't fight it, Chet. You know as well as I there's still something between us. There always will be.'

High heeled, knee-length cowboy boots thumped into the sheriff's department. They weren't new, and the leather did crease in certain areas, but it was nevertheless weathering the wide-ranged usage. Vicky pushed the glass door open, and her outfit immediately earned her a complimenting whistle from the janitor, and a nod from an officer she couldn't recall. She turned to Lucy. 'Hey Lucy,' She smiled at the receptionist, curiously peeking in to see the TV broadcasting the newest soap opera. Victoria stopped to watch the situation unfold - she got hooked on the entangled relationship drama last night, when she was flicking through the channels at the Great Northern. She cleared her throat and turned back to Lucy. 'I believe Sheriff Truman told you that I'll need a lab at the station. Which is the unlucky room I will evade?' Lucy let out the breath she was holding in; probably from the fear that she might be humiliated by yet another scientist, but she was relieved to find that Miss Davis had manners. In fact, it was the first time she wasn't talked down to.

'I was hoping we would have breakfast together,' The agent noted when he stepped into the impromptu laboratory hours later. There was a slight, but unmissable resentfulness in his usually pleasant tonation, and Victoria couldn't help but chuckle. She walked past him to file away a folder. 'You gotta rise earlier, Dale.' His eyes wandered to the hem of her skirt dancing around just above her knees, showing a bit of her thighs. He knew this slight 'indecency' was more so due to her young age and her own perception of herself. She complained at some point that a longer skirt would make her look smaller and stockier - which wasn't true, but it never occurred to Cooper to oppose. He felt the urge to move his hands, so he buried them in his pockets. 'How's the evaluation going?' 'Calmly,' The woman noted in a surprised tone as she returned to her seat. 'We got back the match from the database for the ropes. The twine on the upper arm is pretty common, Finley's Fine Twine.' 'What about the ones on her wrist?' 'No match yet,' She shook her head. 'But the scars on her shoulders, they are bird bites.' 'Bird bites?' His eyebrows grew closer. 'Yeah… I had a dream, and… Anyway, it turned out to be correct. They are still running it through the database, but the results should be here soon,' Her slip of tongue made Cooper's heart flutter. He knew how methodical she was, and could recall many of their conversations about the topic - how dreams and unorthodox methods can further the investigation -, and Vicky often remained on the questioning side. Yet now, it seemed as though she finally understood what he was trying to tell her for so many years. 'The reconstruction of the plastic object found in her stomach is in progress,' She followed, not allowing silence to settle between them. 'The computer gave me a run for my money when I tried to assemble it,' Vicky eased her own tension with a smirk, then took an emerald green notebook into her hands. 'What about you, where the case is going?' 'I've met Dr Jacoby last night, visiting Laura Palmer's grave,' The agent leaned against the edge of the desk, while she scribbled down his observations. She realigned the desk lamp to illuminate the pages. 'Do you consider him a suspect?' 'Well, his name does start with a J…' Coop contemplated. 'He is suspicious, but he doesn't strike me as the type for it. I had him in for questioning this morning, in fact, he just left,' He straightened his tie. 'Laura was his patient, if I recall. Did you try to get something out of him about their sessions?' 'He was unwilling.' 'Of course,' She scoffed. 'But he knew about Laura taking cocaine. His psychological assessment deemed it as a good sign.' The pen in Victoria's hand stopped abruptly, and she raised her eyebrow at her colleague: 'He thought a seventeen-year-old sniffing cocaine for her mental health issues is a good thing?' 'He apparently had that opinion I'm afraid,' The man sighed. 'I'm so glad there are people like this in the world we can trust with our deepest issues,' She noted sarcastically, taking a sip of her coffee. 'What else? How'd that secret meeting with the boys go?' 'You know about the organization?' His jaw dropped and leaned ahead. 'Now I do,' She replied with a mischievous grin. 'To be fair, it is a close-knit community in a secluded area. There's bound to be a secret society of some sort, protecting the values of the community from outside attacks. And I heard you leaving the hotel not long after we said goodnight.' 'You'd be a wonderful detective,' Dale smiled with proud amazement. His conclusion earned a light blush from his colleague, but she was quick to brush it off. 'So, do I get a run-down on it or am I too much of a girl?' 'They had Bernard Renault in for questioning; he's the younger brother of Jacques Renault. They are smuggling cocaine over the Canadian border, but he was unwilling to cooperate. Still, he isn't the sharpest tool in the shed.' 'What else about Doctor Jacoby? Did he say anything else?' 'He saw a red Corvette the night Laura Palmer died. Harry said it must be Leo Johnson's.' 'If we confiscate it can I take it for a test drive?' Vicky crossed her legs as she sunk comfortably into her chair. 'Doesn't it contradict the rule of not disturbing the crime scene?' The agent retorted, but she was quick to remind him: 'I still have your greasy thumb filed under evidence for the Tallak case. Don't play with me.' 'Did you speak to Albert today?' He enquired. 'In the morning, but not since. Why?' 'He wants Sheriff Truman fired,' Coop explained. 'He handed in an OOJ and an AFO to Gordon.' 'Ah, Dale, I don't wanna be part of this...' Vicky pulled her mouth to the side. 'Coop,' Sheriff Truman stepped into the room. 'Hawk found the one-armed man.' 'Be right there, Harry,' The agent raised his palm then turned back to the woman. 'Please. For me.' 'Oh, alright… I'll talk to Albert,' She promised and Cooper's face lit up before the two men darted out. Victoria sighed as she returned to her work, but not before laying out a detailed list of things in her head: a list of things the agent better do to make things even. She knew she'd never hand that list in.

After a while, the lines blended together, regardless of how many times she blinked. She instinctively reached for the pack of cigarettes lying just across the table, only to find it empty. 'Typical,' She muttered to herself, brushing a strand of hair from her face, then checked the time. It was already past one. Vicky grabbed her wallet and her coat. On her way out, she stopped in front of the reception boot. 'Lucy, wanna come along for lunch?' 'I can't,' The receptionist whined. 'Sheriff Truman is out and I can't leave when they're not around.' 'Oh… Anything from the Double R, then?' 'A tuna sandwich would be nice.' 'A tuna sandwich to be delivered. Gonna grab lunch together some other time.'

'Tuna sandwich…' Vicky smiled to herself as she got into her car. Immediately, she shivered and drew her coat closer together. She was quick to start the car, hoping it would warm up during that short ride. While driving, she was reminiscing over a childhood friend of hers - Anne Marie and Lucy showed an uncanny resemblance, not in their features, but in their character. Anne Marie had dark hair and eyes, and hated tuna with all her might, but she was an avid fan of love stories. They frequently snitched their mothers' erotica novels only to stay up way into the night, reading each paragraph with crimson cheeks and excitement. Anne Marie was maturing physically at a much quicker rate, and she was only twelve when she was...

Vicky stepped into the break at the red light she almost passed by.

Love did not turn out to be anywhere near that glorified image they formed in the attic of the vacation house. It was not filled with the thrilling mystery that sent butterflies to their stomachs. It didn't take their breath with passion and soft words. It didn't warm their limbs with the softness of the July sun or shock them like the freshness of the spring they jumped into from the heat. It wasn't ultimate. It wasn't lasting. It wasn't happy.

It wasn't real.

Victoria arrived at the Double R and rushed in to wash the dreadful taste out of her mouth. A nice cup of joe should do the trick.

She thumped down into the barstool with such a force it let out a creek. Norma was quick with a strong brew and her red lips widened into the blissful smile of a mother. 'Good afternoon, Miss Davis. Tough night?' 'Nah, night was fine. Must be this damned weather.' Vicky sighed. 'How are you, Norma?' The woman tensed visibly at the question and there was no sign of the previous smile on her face. She caressed the coffee pot in her hand. 'My husband's due a hearing… About his parole.' 'Oh,' The forensic scientist added. 'And you, um, expecting him home?' 'Of course,' Norma replied dryly, but the very next second she followed as if the little innuendo didn't happen. She was a professional in her own right. 'What can I get you, Miss Davis?' 'Damn I didn't even think about it… It will be a tuna sandwich on the go and... Let's make that two, please.' 'Two tuna sandwiches,' The woman nodded and disappeared into the kitchen.

The more she drank from her coffee the more she contemplated about lips. The lips of a certain individual to be exact. Wondering about the words those lips formed yesterday. Seeing them as closely as years before… Wondering about whether they still taste the same…

'My log has something to say to you,' The sentence was embroidered with loud chewing. Vicky glanced up. She was confronted with a pair of big, strong glasses and a pouted lip. A log rested gently cradled in the arms of the woman next to her. She didn't even give Victoria any time to reply or oppose. 'There are bruises that stay on the skin forever. Others remain on the soul. Innocence is taken from those who rob others of it,' The lady chanted, then resumed to chewing whatever she had in her mouth. 'Margaret!' Norma scolded the woman. 'Don't scare Miss Davis with that nonsense!' To which the woman only spat the pine resin on the counter, and forcefully darted out.

As Victoria was driving back to the police station, the sun peaked out twice - maybe even three times - from the clouds. Two tuna sandwiches on the passenger seat: one whole and one barely touched. After the initial hunger, her stomach dropped again as she replayed the words of the old lady. Was she going mad? What did the woman with the log know? It wasn't the absurdity of the riddle that upset her.

What did upset her was that it made way too much sense.

[labtron]

Cell Strainers are compatible with standard 50mL centrifuge tubes, thus can be used for many applications including isolating cells and removing clumps or debris. Extended grip enables aseptic handling. Packaged sterile (gamma irradiated), non-cytotoxic, DNase, RNase and pyrogen free.

[healthcare00897]

Hematology Market to Exhibit Steadfast Expansion During 2016-2026

Hematology is a branch of medicine which involves the study of blood in health and diseases. Individuals may get affected by several blood related diseases such as blood cancer, anemia, bleeding disorders that includes hemophilia, blood clots, and some others. Hematology includes the problems with the red blood cells, white blood cells, platelets, bone marrow, spleen, lymph nodes, blood vessels, and proteins involved in the clotting and bleeding. A Hematologist is a medical doctor who deals with diagnosis, treatment, and overall management of individuals with blood disorders. The specialists use the hematology instruments for testing, counting, analyzing and measuring of red blood cells, platelets, and white blood cells. These instruments are used for regular and critical testing in clinical laboratories, and further helps to provide the solution to physicians and healthcare providers.

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Growing population with blood related disorders globally is driving the hematology market

According to data given by Leukemia and Lymphoma society (LLS) in 2015, around 9.8% of the population in the United States was diagnosed with leukemia, lymphoma, and myeloma. The data given by National Hemophilia Foundation shows that approximately 400,000 people are suffering from hemophilia in U.S.. Growing population with the blood related disorders is the major factor driving the growth of hematology market. The hematology instruments are showing the transition from traditional instruments to semi-automated instruments and to the recent automated instruments. For instance, Beckman Coulter’s automatic hematology analyzer Unicel DxH slidemaker strainer cellular analysis system has a ‘load and go’ feature that provides the most advanced slide making technology. This analyzer is supported by DxH SMS software that is helping to increase the productivity of diagnostic laboratories. Adoption of this automated instruments by diagnostic laboratories is also owing to the growth of hematology market. Additionally, some advancements in the research areas such as genetic therapies, stem cell research, proteomics, pharmacogenomics, and bleeding disorders, is the another factor contributing to the progress of hematology market. However, the high cost of hematology instruments, stringent and time consuming regulatory policies for hematology analyzers, and hematology product recalls are some restraints that might hinder the growth of hematology market.

Slide strainers are extensively used by doctors and lab technicians owing to the major share of this segment in hematology market

The global hematology market is segmented by products, by applications, by end -users and by region

On the basis of product, the hematology market is segmented into

   Hematology analyzers

   Flow cytometers

   Cell counters

   Slide strainers

   Coagulation analyzers

   Hematology testing

   Centrifuges

  HemoglobinometersDD

   Others

On the basis of application, the hematology market is segmented into

   Infectious diseases

   Blood screening

   Diabetes

   HIV

   Cancer

   Cardiovascular diseases

   Others

On the basis of end -users, the hematology market is segmented into

   Diagnostic laboratories

   Hospitals

   Clinics

   Research and development centers

   others

Rising number of advanced clinics in Asia Pacific is contributing to the growth of hematology market in this region

Regional segmentation of global hematology market by Coherent Market Insights comprises of North America, Latin America, Europe, Africa, Asia Pacific, and The Middle East. Availability of a large number of diagnostic centers and adoption of highly adopted hematology analyzers by the laboratories is owing to the domination of North America in the hematology market. Rising population with blood disorders and investments made in research and development are some of the important factors for North America to hold the largest share in hematology market. Asia Pacific is also expected to drive the growth in hematology market followed by North America and Europe. Growing patient population, rising demand for technologically advanced medical devices, and rise in a number of advanced clinics, are some of the driving factors of hematology market in this region.

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Major players are trying to expand their product portfolio to grab the maximum share in the global hematology market

Key business players operating the global hematology market includes Abbott Laboratories, Sysmex Co., Beckman Coulter, Danaher, Mind ray Medical International Limited, Siemens Healthcare, Roche diagnostics, Bio Rad laboratories, and Sigma Aldrich Co.  Companies are even adopting the strategy of merger and acquisition to sustain in the global hematology market.

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[crimsonfantrash-blog]

Don’t Forget - Sans x Gaster (Human AU)

Chapter Three - Phone Calls

Sans came into the lab at around seven fifty in the morning, much to Gaster's surprise. Early, his first two days? This was beginning to become too good to be true.

"Three sugar, two cream?" Gaster asked when Sans had set the mug of hot coffee on his desk.

"Three sugar, two cream." Sans confirmed. Gaster nodded, sipping his coffee. Sans had made it perfectly, just like yesterday. He could get used to having Sans around. His co worker yawned before going to his desk. "What are we doing today?"

"I'm not sure yet. Asgore usually comes by and tells me what I'm supposed to be doing. I suppose the goal is the same as always, so he saw no use." Gaster replied, setting the mug of coffee down and digging through papers on his messy desk.

"What's the goal?" Sans asked. Gaster looked at his assistant.

"To get to the surface." He answered. "The only way we can do it is if we have seven monster souls, but the King's child is a monster. He would never be able to take the soul of an innocent monster. I- we have to find some other way out."

Sans seemed to make an uncomfortable face. "What if we get there, and it sucks?"

"We have to try." Gaster replied. "No matter what, we have to try."

Sans nodded a little, focusing his attention to his desk. Huh. He had papers on it. Didn't have those yesterday. "I mean, it doesn't appeal to me personally, but okay."

Gaster sipped his coffee, closing his eyes. "Today, we're going to work on a machine I've been working on sporadically."

"What does it do?" Sans asked. Gaster leaned back in his chair.

"It erases any memory you want to forget." Gaster explained. "I've almost finished it. I just need a few more parts."

"Sounds a little too good to be true, dude." Sans replied skeptically.

"Anything is possible with the proper knowledge and materials to make it a reality." Gaster replied. "It has to work."

"What if it doesn't?"

"You ask too many questions." He chuckled.

Once they had started working on it, Sans sat on the sidelines beside the toolbox, passing Gaster whatever he had needed as they talked. "What do you think the surface is like?"

"Spacious, surely. Much better than this cramped little cave we live in, I would assume. Plants, animals... The kinds you've seen in books. And monsters. Probably loads of them."

"How many monster do you think there are?"

"There isn't any real way of knowing, but I'm sure if you measured the diameter of the Earth- I read in a book from the surface that it's seven thousand, nine hundred seventeen and a half miles- and then measure the amount of land there is, you could estimate about how many monsters there are up there. My guess is a few billion."

Sans blinked. "You know too much, dude."

"Screwdriver." The scientist said, holding his hand out. Sans passed him the screwdriver, resting his chin in his hand as he blew hair out of his face. "You need a haircut."

"I like it this way. It hides my face." Sans replied.

"Why would you want to hide your face?" Gaster asked. He was puzzled.

"Because I'm ugly." Sans answered.

"No, you're not." Gaster objected. Sans frowned a bit. "I saw your picture on your ID, your hair is barely covering your face in it. You're not ugly. You look fine."

"I dunno, man. I'm kinda ugly." Sans said. "Doesn't matter what you say, I'm ugly."

The scientist sighed. "Wrench."

~~~~~~~~~~

Gaster closed the door behind him, leaning against it as he sighed. What a busy day... He loosened his tie, and kicked off his shoes before heading upstairs to his study. He sat at the desk, leaning back in his chair. The only sound in the room was his breathing and the tick of an old grandfather clock. A picture frame that sat on the desk burned holes into his soul. He turned it around. Not today.

Tick, tock, tick, tock. The clock wouldn't shut up, and Gaster was painfully aware of every second that went by. His mind screamed at him to get up. To do something. With haste, he pulled his phone out and scrolled through his contact list.

Asgore Sans Toriel

Really...? He only knew three people...? Oh, well... His finger hesitated over Sans' name, before he pressed it. He held the phone up to his ear, biting his nails. It rang a few times before there was the sound of someone picking up. "Sup?" Sans' voice came over the line. Thank God.

"I, uh..." Gaster swallowed the lump forming in his throat. "Wanted to call to say hi."

"Uh, we just saw each other not even twenty minutes ago, Gast." Sans said. Gaster could basically hear the other male's confusion as to why his boss would call him not even twenty minutes later. "But, hi."

"Hi." Gaster said. And then the call became silent.

"I'm still walking home, would it be okay if I called you back when I start making dinner?"

"Yes, of course, that is fine." Gaster replied. He tried to shove all the anxiousness in his voice down. "I will talk to you later."

"Bye, Gaster."

"Bye."

Click. The call ended almost as soon as it had been started. Gaster checked the call log. He had made more calls to his co worker in the past two days than he had made to Asgore last week. Three calls with Sans verses one with Asgore. The scientist frowned. This was very strange...

~~~~~~~~~~

He kicked his shoes off (an old pair of sneakers he had pulled out of the closet once he realized wearing slippers to work wasn't all that good of an idea) and flopped onto the couch. He could hear his little brother and Undyne upstairs, probably playing with Pap's action figures and much too busy to realize the man of the house was home.

When he finally stood from the lumpy, uncomfortable couch, he walked into the kitchen. May as well start on dinner... He pulled a box of mac and cheese out of the cupboard. He didn't even need to read the directions to know exactly what he was doing. Once the pasta was in the pot, and the stove was hard at work, bringing the water to a boil, Sans pulled his cell phone out, and called Gaster back. It barely had a chance to do half a ring before the other male picked the phone up. "Hey." Sans said. He leaned against the wall.

"Hello." Gaster replied. Sans couldn't quite place the vibes the slightly older male was giving off, but he could tell his boss wasn't exactly happy, just from the tone of his voice, and the conversations they'd had throughout the day. He chose to ignore it, however. It wasn't his business, and he doubted Gaster was the type to open up like that to people who were basically strangers.

"What's up, dude?" Ah, jeez, had he really just asked one of the most brilliant people in the Underground 'what's up, dude?'? How embarrassing... Little too late to take it back, however, so he bit his tongue as his cheeks flushed pink, and prayed that Gaster wouldn't think he was weird, or something.

Thankfully, Gaster had ignored the informality of that sentence. "I'm just a bit bored, honestly." He didn't sound bored. He sounded borderline upset. Then again, he looked like the type who would attend a wedding wearing all black, or attend a funeral and be envious, wishing it was him who was getting lowered six feet under. "What, uh, what are you up to?"

The fact that his co worker was interested in what he was doing was a bit strange to Sans. They were barely even friends yet, and here they were, talking on the phone as if they had known each other for much longer than they actually had. "I'm making dinner. Mac and cheese."

Gaster felt everything in him scream to end the conversation and hang up, before he embarrassed himself, but, for whatever reason, he continued. "I'm just ordering a pizza. I don't feel like cooking tonight."

"I've never had pizza before." Sans said. The scientist could hear him laugh nervously. "Never really been financially well off enough to have pizza. Is it good?"

Gaster nodded, but then reminded himself that Sans couldn't see him. "Yes, I think so. It is my favourite food."

"You struck me more as a fancy food kind of guy. Pizza isn't all that fancy, I don't think." Sans  replied.

"Why do I strike you as a fancy food kind of guy?" Gaster asked.

"Well, I dunno. You became the Royal Scientist when I was eleven, and you looked really important, and I'd always thought important people liked fancy things." Sans said. "I suppose it's a weird mindset to have now that I'm an adult, but when I met you last week, you still gave me fancy person vibes."

Gaster opened his mouth to rebuttal, but then remembered he had a wine rack in his kitchen, and was probably going to listen to classical music while eating his pizza and drinking a glass of said wine. That felt very... Snobby. He fixed his glasses and thinned his lips into a line. "Yes, I suppose you're right." Gaster said. He heard loud sounds on Sans' end of the phone.

"Papyrus, come back here!" "You'll never catch me alive!!"

"Guys, no running and yelling in the house!" Sans had yelled. "Sorry, my brother and his friend are being loud."

"Children are usually very loud." Gaster said.

"NGAAAAAH!! COME BACK HERE!!!"

"NEVEEEERRRR!!!!"

... But not quite that loud. "Guys, I'm on the phone! Keep it down!" Sans yelled. "I think I should hang up, she's got him in a head lock, and this usually doesn't end very well." Sans said. The scientist felt... concerned. He didn't know who to be more concerned about; himself, for associating with Sans, Sans, who had to deal with this, his little brother, who he didn't even know, for being in a headlock, or his brother's friend for putting him in said headlock.

"I have to call the pizza place, anyways." Gaster said. "See you at work tomorrow, Sans."

"See ya."

Click.

"Get off, get off, get off!!" Papyrus yelled, struggling. Sans came in, and broke it up, holding Undyne back.

"Alright, that's enough. Play nicely, or don't play at all." He scolded. Undyne crossed her arms.

"Well, it's not my fault he isn't tough enough." She said.

"Undyne, play nice with my brother." Sans said. He returned to the kitchen.

The pasta had boiled. He strained the water out with a strainer, put the pasta back in the pot, and added the cheese sauce. He gave a bowl of mac and cheese to his brother and Undyne, before getting a bowl for himself and going up to his room. He sighed before eating. Peace and quiet...

As soon as Gaster's pizza had arrived, he paid the delivery person, and set the box on the table. Maybe he'd skip on the classical music part and just skip to the wine... He was feeling rather self conscious now after that conversation with Sans. As the scientist ate his dinner, he kept wondering what had possessed him to make conversation with his co worker in the first place. He sipped his wine. He supposed... Sans was just very interesting, compared to his boring life. Yes, that must have been it.

((This chapter was kind of challenging to write. I just couldn't find the words for this one. Had to walk away from it a few times.

I'm hoping to update this at least once a week, but if no one reads it, I'm not so sure that would be the best use of my time. I'm working on a few things right now, so we'll see.))

[drsciencelab-blog]

Dr. Scientific Lab offers surestrain premium cell strainer system that quick and safe to use solution for detaching, isolating and straining cells from clusters and tissues. Get details.

[industryupdatenews]

Histopathology Testing Equipment Market 2020: Business Trends, COVID - 19 Outbreak, Emerging Technologies, Growth Opportunities and Regional Forecast

Study on the Global Histopathology Testing Equipment Market

Fact.MR, recently published a market study which indicates that the global Histopathology Testing Equipment market is anticipated to grow at a CAGR of ~XX% during the forecast period (2018-2028). The growth of the Histopathology Testing Equipment market is predominantly driven by rising demand for histopathology lab instruments from multiple end-use industries.

Due to the pandemic, we have remembered an uncommon segment for the Impact of COVID 19 on the Scientific Research Satellites Services Market which would make reference to How the Covid-19 is influencing the Market Trends and Potential Opportunities in the COVID-19 Landscape, Covid-19 Impact on Key Regions and Proposal for Histopathology Testing Equipment Market Players to Combat Covid-19 Impact.

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The presented study addresses the following queries related to the Histopathology Testing Equipment market:

1.      Why is the demand for product 1 expected to witness considerable growth over the forecast period?

2.      How will progress in technology influence the growth of the Histopathology Testing Equipment market in the upcoming years?

3.      Which region is likely to emerge as the most lucrative pocket for market players?

4.      What are the recent trends that are likely to impact the growth of the Histopathology Testing Equipment market in the near future?

5.      Which market players are expected to have a strong global presence in the Histopathology Testing Equipment market?

Competitive Landscape

The presented market report dives deep into understanding the business strategies adopted by leading market players in the global Histopathology Testing Equipment market. Further, the SWOT analysis for leading market players is enclosed in the report along with the revenue share, pricing analysis, and product overview of each company.

Detailed profiles of the providers are also included in the scope of the report to evaluate their long-term and short-term strategies, product portfolio of Histopathology Testing Equipment manufacturers, and recent developments in the Histopathology Testing Equipment market space. Some of the key players analyzed are:

·         Sakura Finetechnical Co., Ltd

·         Merck KGaA

·         Advanced Cell Diagnostics, Inc.

·         Abbott Laboratories

·         Cardinal Health, Inc.

·         Abcam

Global Histopathology Testing Equipment Market – By Product

·         Tissue Processor Equipment

·         Tissue Embedding Equipment

·         Slide Strainers Systems

·         Cover slipper Systems

·         Microtome & Cryostat

·         Microscopes

·         Reagents & antibodies

·         Probes

Global Histopathology Testing Equipment Market – By End Use

·         Hospital based laboratories

·         Diagnostic Centers

·         Research Organizatio

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Global Histopathology Testing Equipment Market – By Region

·         North America (U.S., Canada)

·         Latin America (Brazil, Mexico, Argentina, Rest of Latin America)

·         Europe (Germany, Italy, France, U.K., Spain, Benelux, Russia, Rest of Europe)

·         East Asia (China, Japan, South Korea)

·         Japan

·         APEJ (China, India, Indonesia, Thailand, Singapore, Australia & New Zealand, Rest of Asia Pacific)

·         South Asia & Oceania (India, Thailand, Indonesia, Malaysia, Australia & New Zealand, Rest of South Asia & Oceania)

·         Middle East & Africa (GCC Countries, Turkey, Northern Africa, South Africa, Rest of Middle East & Africa)

The data scrutiny for the global Histopathology Testing Equipment market is estimated in terms of value and volume consumption. To arrive at the volume consumption of Histopathology Testing Equipment, production data of countries producing raw materials across the globe has been taken into consideration. In addition, the production of application of Histopathology Testing Equipment in top producing countries is also tracked for benchmarking purposes. Furthermore, Fact.MR estimated volume data on the consumption of Histopathology Testing Equipment for several countries by understanding the demand and supply of Histopathology Testing Equipment. It includes production, growth, volume and value sales, transition, pricing, population, consumer preference, and consumption of Histopathology Testing Equipment among end user verticals.

Fact.MR then determined the volume consumption of Histopathology Testing Equipment across various regions such as North America, Latin America, Europe, Asia Pacific, and Middle East and Africa. Forecasting is done on an internal proprietary model using different macro-economic, industry-based demand driving factors impacting the market and its forecast trends, by identifying and allocating a weighted score to the forecast factors that influence the demand for Histopathology Testing Equipment. These factors were the representative of an entire value chain, as well as macro-economic indicators such as production have been taken into consideration to arrive at the volume consumption of Histopathology Testing Equipment in respective countries.

The weighted average selling price for Histopathology Testing Equipment was considered to estimate the market size for top Histopathology Testing Equipment consuming countries. These prices were captured in their respective countries, and then converted into USD to offer forecasts in one consistent currency standard.

Given the characteristics of the market, Fact.MR triangulated the data based on supply side, demand side, and dynamics of the global Histopathology Testing Equipment market. To develop the global Histopathology Testing Equipment market forecast, Fact.MR analyzed various factors to understand their respective impact on the target market. However, quantifying the market across the abovementioned segments is more a matter of quantifying expectations and identifying opportunities rather than rationalizing them after the forecast has been completed.

It is imperative to note that, in an ever-fluctuating economy, we not only provide forecasts in terms of CAGR but also analyze on the basis of key parameters, such as year-on-year (Y-o-Y) growth, to understand the predictability of the market and identify the right opportunities.

Another key feature of this report is the analysis of the global Histopathology Testing Equipment market and the corresponding revenue forecast in terms of absolute dollar opportunity. This is usually overlooked while forecasting the market. However, absolute dollar opportunity is critical in assessing the level of opportunity that a provider can look to achieve, as well as to identify potential resources from a sales perspective in the global Histopathology Testing Equipment market.

To understand key segments in terms of their growth and performance in the global Histopathology Testing Equipment market, Transparency Market Research has also presented a market attractiveness index. The resulting index should help providers identify existing market opportunities in the global Histopathology Testing Equipment market.

The report covers an in-depth analysis of all components of the value chain in the global Histopathology Testing Equipment market. In the final section of the report on the global Histopathology Testing Equipment market, a competitive landscape is included to provide a dashboard view of global Histopathology Testing Equipment manufacturers.

Regional Assessment

The extensive study on the Histopathology Testing Equipment market pinpoints the different factors that are likely to influence the prospects of the Histopathology Testing Equipment market in each region. The different regions covered in the report include:

Application Analysis

The report offers crucial insights related to the various applications of the Histopathology Testing Equipment along with the Year-on-Year growth analysis of each application.

Decisive Information Enclosed in the report:

·         The scenario of the global Histopathology Testing Equipment market in different regions

·         Current market trends influencing the growth of the Histopathology Testing Equipment market

·         Factors expected to hinder the growth of the global Histopathology Testing Equipment market

·         Micro and macro-economic factors shaping the growth of the market in different regions

·         Key strategies adopted by players to gain a competitive edge in the Histopathology Testing Equipment market

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[uberstrainer]

Overhead Rotation and Its Benefits: Why It Matters in the SnapCap Steel Extraction Strainer

In many lab-based processes, the tools used can significantly affect the quality, accuracy, and efficiency of the outcome. Whether preparing a sample for analysis or isolating specific particles from a mixture, the right equipment can streamline workflow and reduce the risk of contamination or sample loss. Among these essential tools, the best Lab Cell Strainers play a major role in optimizing sample preparation and filtration. However, when it comes to chemical extraction and particle separation techniques from solids, tools like the SnapCap Steel Extraction Strainer stand out due to their unique design features—especially the ability for overhead rotation.

This feature is not just about convenience. Overhead rotation directly contributes to a more effective extraction process, ensures even contact between the solvent and the solid, and enhances the reliability of the results. In this blog, we’ll explore how the SnapCap Steel Extraction Strainer functions and why overhead rotation is a key benefit worth considering for researchers and labs alike.

Understanding the SnapCap Steel Extraction Strainer

Before diving into the advantages of overhead rotation, it’s helpful to understand how the SnapCap Steel Extraction Strainer is designed. The device features a metal strainer integrated into a snap cap, forming a compact and practical tool for extracting chemicals or particles from solid matter. It includes a 9 cm³ internal volume, which allows for a decent amount of material to be processed at once.

What makes this product particularly effective is its airtight elastomer sealing, which prevents leaks or exposure to air during processing. This is especially important when working with volatile solvents or sensitive materials that could degrade in open environments.

The Role of Overhead Rotation

The SnapCap’s ability to be rotated overhead brings several advantages to the table. It is more than just a mechanical feature—it’s a functional aspect that impacts how well the strainer performs during extraction processes.

1. Enhanced Mixing for Efficient Extraction

One of the biggest benefits of overhead rotation is improved mixing. When a strainer is rotated overhead, the contents inside are agitated continuously, ensuring that the solvent makes full contact with the solid particles. This increases the efficiency of chemical extraction and helps reduce the time needed to obtain a usable sample.

In a static setup, where the solvent simply sits around the solid, extraction can be uneven or incomplete. Overhead rotation removes this limitation, allowing the solvent to access more surface area consistently.

2. Improved Contact Between Solids and Solvents

Consistent rotation ensures that the solid material inside the SnapCap Steel Extraction Strainer is always exposed to fresh solvent. This continuous interaction prevents layering or compaction of solids at the bottom, which can block effective penetration.

The more uniform the contact, the better the chances of complete extraction. For researchers working with valuable or limited materials, this ensures that no sample goes to waste and the most is made from every run.

3. Better Results in Less Time

In most laboratory environments, time is a critical factor. Faster extraction means quicker analysis, testing, or production. With the SnapCap’s ability to rotate overhead, labs can speed up the filtration process without sacrificing quality or yield.

Instead of waiting for passive extraction methods to complete, overhead rotation accelerates the process, improving productivity across the board.

4. Consistent Sample Quality

Whether you're using a cell strainer for biological samples or a chemical strainer like the SnapCap, consistency is key. Overhead rotation reduces variability between samples by ensuring that each extraction is carried out under the same dynamic conditions.

This is particularly important in settings where precise measurements or sensitive results are required. The more predictable the method, the more reliable the data.

5. Less Manual Intervention

Manual shaking or tilting of tubes is a common workaround in labs that don’t use rotating devices. This method is not only inconsistent but also labor-intensive and prone to human error. The overhead rotation feature of the SnapCap Steel Extraction Strainer automates this process, reducing the burden on lab personnel while improving outcomes.

With reduced handling, there's also less risk of contamination or sample disturbance—especially useful in sterile environments or when processing hazardous materials.

How It Compares to the Best Lab Cell Strainers

Although the SnapCap is designed for chemical and solid particle extraction, its principles overlap with those of the best Lab Cell Strainers. Both aim to provide clean, usable samples by separating unwanted particles from the material of interest.

Where lab cell strainers focus more on biological samples and cell separation technology, the SnapCap Steel Extraction Strainer brings a similar level of efficiency and reliability to chemical processes. Researchers who appreciate the benefits of a good lab cell strainer will recognize the value of overhead rotation in enhancing extraction methods.

Applications in Research and Industry

The SnapCap Steel Extraction Strainer isn’t just for routine lab work. Its design and functionality make it suitable for a range of applications:

Pharmaceutical research: For extracting active ingredients from solid compounds

Environmental testing: To isolate particles from soil or sediment samples

Material science: For solvent extraction from composite materials

Food testing: When analyzing extracts from grains, seeds, or solid foods

In each of these fields, overhead rotation improves repeatability and accuracy, which are essential for quality control and research integrity.

Integration into Existing Workflows

One concern for any lab introducing new equipment is compatibility. Fortunately, the SnapCap Steel Extraction Strainer fits easily into existing lab protocols without the need for significant changes. Its compact design and overhead rotation feature can be combined with standard rotation devices or custom setups, depending on lab requirements.

Moreover, just as the best Lab Cell Strainers are valued for their ease of use and flexibility, the SnapCap offers similar user-friendly features that make it an easy addition to most research settings.

How Overhead Rotation Adds Long-Term Value

Using overhead rotation isn’t just about improving current experiments. Over time, this method can lead to:

Reduced material costs: Better extraction means less waste.

Higher throughput: More samples processed in less time.

Improved data accuracy: Uniform conditions produce consistent results.

Safer lab environments: Less manual handling minimizes risk.

These benefits can directly impact operational costs and research quality, making the SnapCap Steel Extraction Strainer a cost-effective investment for many labs.

Conclusion

The SnapCap Steel Extraction Strainer is a valuable addition to laboratories looking for efficient and reliable chemical extraction tools. Its overhead rotation capability offers a clear advantage by improving mixing, reducing extraction time, and increasing sample consistency. For researchers already familiar with the reliability of the best Lab Cell Strainers, the SnapCap offers the same level of performance in solid-to-liquid extraction processes.

Incorporating this device into your lab's workflow can elevate your extraction procedures while maintaining the quality and precision your work demands. Whether you're in pharmaceuticals, environmental science, or materials testing, the SnapCap Steel Extraction Strainer is designed to meet modern lab needs with dependable results.