#lab instrument
Explore tagged Tumblr posts
laboidasia · 11 months ago
Text
How to Ensure Accurate Results with Semi-Automatic Rotary Microtome
Tumblr media
Semi-automatic rotary microtome is machines that cut very thin slices of tissue so scientists can look at them under a microscope. To get the best and most accurate results from these machines, you need to follow some simple steps.
Tips to Ensure Accurate Results with Semi-Automatic Rotary Microtome
1. Check the Machine Regularly
You need to make sure your microtome is working correctly. To do this, you should calibrate it often. Calibration means adjusting the machine so it cuts at the right thickness. Before you use the machine each day, make sure it's set up correctly by checking it with special blocks or standards. If the slices aren't the right thickness, adjust the settings until they are.
2. Keep the Blades Sharp and Clean
The blades on the microtome must be sharp to cut well. If the blades are dull, they won’t cut the tissue properly. Always replace blades that are not sharp or have any damage. Clean the blades after you use them to remove any leftover tissue. Use the cleaning solutions that come with the machine to avoid hurting the blades.
3. Prepare Tissue Samples Correctly
Before you cut the tissue, make sure it’s prepared properly. This means the tissue should be fixed and put in a supportive material like paraffin. Fixing keeps the tissue from going bad, and embedding it helps it stay firm for cutting. Make sure the tissue is placed correctly in the material so it cuts evenly.
4. Set the Right Thickness
Decide how thick you want the slices to be before you start. Use the machine's controls to set this thickness accurately. Always use the same thickness for all your slices to keep them consistent. If you need to change the thickness, do it slowly and check the new setting with calibration blocks.
5. Watch the Environment
The room where you use the microtome should have stable temperature and humidity. Too much heat or cold can affect how well the machine works. Make sure the machine is not near drafts, direct sunlight, or heaters. Keeping the environment stable helps the tissue stay at the right firmness for cutting.
6. Check the Slices Often
While you are cutting, keep an eye on the slices to make sure they are right. Look for any problems like uneven cuts or tears. If you see issues, it might mean the machine settings or blades need adjustment. Regular checking helps you fix problems early and ensure your slices are good.
7. Clean and Maintain the Microtome
After you use the microtome, clean it to keep it in good shape. Follow the cleaning guide that comes with the machine. Check the semi-automatic rotary microtome regularly for any worn-out or broken parts. Replace any parts that are damaged to keep the machine working well.
8. Train and Help Users
Everyone who uses the microtome should know how to use it correctly. Make sure they understand how to set the thickness, handle the blades, and prepare the tissue. Help them if they are new to using the machine. Good training helps prevent mistakes and ensure good results.
9. Keep Track of Results
It’s helpful to write down details about the cutting process. Note the settings you used, the condition of the blades, and any problems you had. Looking back at these notes can help you find and fix any recurring issues, making sure your results stay accurate.
10. Check Quality Regularly
Check the quality of the slices from time to time. Use special samples to make sure everything is working right. Compare your slices to these samples to see if they match. If there are any differences, find out why and fix the problem. Regular checks help keep the machine working correctly.
Conclusion:
To get the best results from a semi-automatic rotary microtome or slide staining machine, you need to take care of the machine and follow some simple steps. Check and calibrate the machine, keep the blades sharp, and prepare the tissue properly. Watch the environment, inspect the slices often, and clean the machine regularly. Train everyone who uses the microtome and keep track of the results. By following these easy steps, you can make sure your microtome works well and gives you accurate slices every time.
0 notes
randomwriteronline · 15 days ago
Text
Bites my leg like a chicken tender. I should write about Artakha and the toa mata post-canon
12 notes · View notes
lethaloptix · 30 days ago
Text
WIP epic strings composition. 🎶
7 notes · View notes
zodiaclifesciences · 1 month ago
Text
4 notes · View notes
hylianengineer · 10 months ago
Text
Running an unfamiliar instrument while no one else is in the lab has me flinching every time it makes a weird noise.
The thing is, most instruments do nothing but make weird noises the entire time they're running.
14 notes · View notes
oktaviaslabyrinth · 1 year ago
Text
Rowan Pokémon Lab // Pokémon Diamond & Pearl (2006)
20 notes · View notes
bubble-jasmine · 2 years ago
Text
Tumblr media
this bitch is called a SCOOPULA and I am SIMPLY AMAZED
71 notes · View notes
starot · 1 year ago
Text
Tumblr media Tumblr media Tumblr media Tumblr media
visited the optics and instrumentation lab recently. not because i had actual work there, but because they have really good air conditioning, and it has been way too hot on campus lately 😮‍💨
our local 7/11 began selling kimbap, and i really enjoy eating it xwx
18 notes · View notes
soulganic · 14 days ago
Text
🧪🎧 In The Lab: Spacey 🌌
Just like stretching before you work out, you have to find the groove before you get down. Here's a little spacey groovy joint.
"Music dominates the universe. It is the prime force. It has given shape to space." - Vangelis
✌️x💙
2 notes · View notes
ad-astra-per-aspera-1389 · 4 months ago
Text
AAAAHHHH
OWAM AND DOROTHEA
ADAM RETURNS TO MISSION CREEK AFTER THE ISLAND AND "ITS NEVER TOO LATE TO COME BACK TO MY SIDE/THE STARS IN YOUR EYES SHINED BRIGHTER IN TUPELO"
I JUST...ADAM'S CHARACTER TOOK A TURN ONCE THE SECRET GOT OUT, AND JUST BEING A NORMAL TEENAGER IN MISSION CREEK HE GOT TO BE HIS GOOFY OPTIMISTIC SELF
SORRY FOR THE CAPSLOCK
4 notes · View notes
lethaloptix · 4 months ago
Text
Here's a dramatic cinematic crescendo I made with the Spitfire LABS Epic Strings pack. Perfect for a suspenseful moment.
Nexus © 2025
7 notes · View notes
kagiura-akira · 2 months ago
Text
I'm gonna say something controversial because it goes against everything I stand for regarding doing research for oneself, but there is nothing I hate more—as a chemist for a contract research organization—than when a client "does their own research."
As in, when a salesperson or even like a small time CEO or CFO looks up how something works and tries to understand it but fails fantastically.
My guy, you hired me to test your samples. I don't need you to tell me how methylcobalamin interferes with arsenic on an ICPMS. If you think Google AI knows better than me, I dare you to click on the links of the summaries it provides and tell me WHERE the skimmed content says this bullshit.
5 notes · View notes
science-sculpt · 1 year ago
Text
Tumblr media
ELISA: A Powerful Tool for Detecting the Invisible
ELISA, or Enzyme-Linked Immunosorbent Assay, has become a cornerstone of medical diagnostics and biological research. This versatile technique allows scientists to detect and quantify minute amounts of target molecules, such as proteins, antibodies, and even viruses, with remarkable accuracy. In this blog, we'll delve into the world of ELISA, exploring its various types, its applications, and the exciting future directions this technology holds.
At its core, ELISA relies on the exquisite specificity of antibodies. Antibodies are highly specialized proteins produced by the immune system in response to foreign invaders. Each antibody can bind to a unique structure, called an antigen, on a specific molecule. In an ELISA, scientists leverage this binding property to create a sensitive detection system.
The 1960s witnessed a surge in interest in immunoassays, techniques that utilize the specificity of antibodies to detect target molecules. One such technique, radioimmunoassay (RIA), developed by Rosalyn Yalow and Solomon Berson, revolutionized medical diagnostics. RIA used radioactively labeled antibodies to detect antigens, offering high sensitivity. However, concerns regarding the safety of radioactive materials fueled the search for a safer alternative. The year 1971 marked a turning point. Independently, Eva Engvall and Peter Perlmann published their work on a novel technique – the enzyme-linked immunosorbent assay (ELISA). ELISA replaced radioactive labels with enzymes, eliminating the safety concerns associated with RIA. Like RIA, ELISA harnessed the specific binding between antibodies and antigens. However, it employed enzymes that could generate a detectable signal, such as a color change, upon interacting with a substrate. This innovation paved the way for a safer and more user-friendly diagnostic tool.
The basic ELISA protocol involves immobilizing the target antigen on a solid surface like a plate well. Then, a sample containing the molecule of interest (e.g., a suspected virus) is introduced. If the target molecule is present, it will bind to the immobilized antigen. Next, an antibody specific to the target molecule, linked to an enzyme, is introduced. This "detection antibody" binds to the target molecule already attached to the antigen. Finally, a substrate specific to the enzyme is added. This antigen-antibody binding is visualized using an enzyme linked to a reporter molecule. When the enzyme encounters its substrate, a detectable signal is produced, such as a color change or luminescence. The intensity of this signal is directly proportional to the amount of antigen present in the sample, allowing for quantification. The beauty of ELISA lies in its adaptability. Several variations exist, each tailored for specific detection needs.
The Four Main ELISA Formats are:
Direct ELISA: Simplicity at its finest. In this format, the antigen is directly coated onto the ELISA plate. A labeled antibody specific to the antigen is then introduced, binding directly to its target. After washing away unbound molecules, the enzyme linked to the antibody generates a signal upon addition of the substrate. Direct ELISA offers a rapid and straightforward approach, but sensitivity can be lower compared to other formats due to the lack of amplification.
Indirect ELISA: Unveiling the Power of Amplification. Similar to the direct ELISA, the antigen is first coated onto the plate. However, instead of a labeled primary antibody, an unlabeled one specific to the antigen is used. This is followed by the introduction of a labeled secondary antibody that recognizes the species (e.g., mouse, rabbit) of the primary antibody. This two-step approach acts as an amplification strategy, significantly enhancing the signal compared to the direct ELISA. However, the presence of an extra incubation step and the potential for cross-reactivity with the secondary antibody add complexity.
Sandwich ELISA: Capturing the Antigen Between Two Antibodies. Here, the capture antibody, specific for one region of the antigen, is pre-coated onto the ELISA plate. The sample containing the antigen is then introduced, allowing it to be "sandwiched" between the capture antibody and a detection antibody specific for a different region of the same antigen. A labeled secondary antibody or a labeled detection antibody itself can then be used to generate the signal. Sandwich ELISA boasts high sensitivity due to the double-antibody recognition and is often the preferred format for quantifying analytes.
Competitive ELISA: A Race for Binding Sites. In this format, the antigen competes with a labeled antigen (usually a known amount) for binding sites on a capture antibody pre-coated onto the plate. The more antigen present in the sample, the less labeled antigen can bind to the capture antibody. Following a washing step, the amount of bound labeled antigen is measured, providing an inverse relationship between the signal and the concentration of antigen in the sample. Competitive ELISA is particularly useful for studying small molecules that may be difficult to directly conjugate to an enzyme.
ELISA's Reach: From Diagnostics to Research. The applications of ELISA are as vast as they are impressive. Let's delve into some key areas where ELISA plays a vital role:
Unveiling the Mysteries of Disease: Diagnostics: ELISA is a cornerstone of diagnosing infectious diseases like HIV, Hepatitis, and Lyme disease. It detects antibodies produced by the body in response to the invading pathogen, providing valuable information for early detection and treatment. Monitoring Autoimmune Diseases: ELISA helps monitor autoimmune diseases like rheumatoid arthritis and lupus by measuring specific antibodies associated with these conditions. Cancer Screening: Certain cancers can be detected by identifying tumor markers, proteins elevated in the blood of cancer patients. ELISA assays are being developed to detect these markers for early cancer screening.
Safeguarding Food Quality: Allergen Detection: Food allergies can be life-threatening. ELISA ensures food safety by enabling the detection of allergens like peanuts, gluten, and milk in food products, protecting consumers with allergies. Monitoring Foodborne Pathogens: ELISA can identify harmful bacteria, viruses, and toxins in food, preventing outbreaks of foodborne illnesses.
Environmental Monitoring: Pollutant Detection: ELISA can detect pollutants like pesticides and herbicides in water and soil samples, contributing to environmental protection efforts. Microbial Analysis: This technique can be used to identify and quantify specific microbes in environmental samples, providing insights into ecosystem health.
Research and Development: ELISA plays a crucial role in various research fields: Drug Discovery: It helps researchers assess the effectiveness of new drugs by measuring drug-target interactions and monitoring drug levels in the body. Vaccine Development: ELISA is instrumental in developing vaccines by evaluating immune responses to vaccine candidates. Basic Research: Scientists use ELISA to study various biological processes by detecting and quantifying specific molecules involved in these processes.
Despite its established role, ELISA is evolving alongside technological advancements. New multiplex platforms allow for the simultaneous detection of various targets in a single sample, boosting efficiency in biomarker discovery and disease analysis. Automation streamlines workflows minimizes errors, and increases throughput, making high-throughput screening feasible in drug development and clinical settings. Miniaturization and portable devices enable rapid on-site diagnostics, providing healthcare professionals with real-time data for quicker interventions. Additionally, ongoing research is improving assay sensitivity, reducing background noise, and expanding detection limits, allowing for the identification of trace analytes and early disease biomarkers with greater accuracy than ever before. Integration of ELISA with emerging technologies such as microfluidics, nanotechnology, and artificial intelligence holds promise for enhancing assay performance, scalability, and data analysis capabilities.
These advancements hold promise for even wider applications of ELISA in the future. ELISA has revolutionized our ability to detect and quantify biological molecules. Its versatility, accuracy, and adaptability make it an invaluable tool across various scientific disciplines. As research continues to refine and innovate ELISA techniques, we can expect even more exciting possibilities to emerge in the years to come. ELISA's future is bright, promising to play a pivotal role in unraveling the mysteries of the biological world and improving human health.
11 notes · View notes
oktaviaslabyrinth · 2 years ago
Text
Akkala Ancient Tech Lab // The Legend of Zelda: Breath of the Wild (2017)
33 notes · View notes
lemonynuggets · 7 months ago
Text
just went through the most evil dentist stereotype procedure ever, I feel like I’m in a stupid horror movie or something
3 notes · View notes
equilrxnlab · 7 months ago
Text
youtube
What Are the Benefits of Using the AKF-100L Double-Glazed Reactor for Advanced Chemical Reactions?
The AKF-100L Double-Glazed Reactor is a high-performance solution for chemical reactions, offering precise temperature control ranging from -120°C to 300°C. It features:
100L material capacity & 60L jacket capacity for efficient heating and cooling.
6 customizable ports for versatile experimental setups.
Stainless steel fluoropolymer-coated stirrer for reliable mixing.
5L constant pressure funnel to enhance reaction efficiency.
Optional explosion-proof control box, explosion-proof motor, and insulation sheath for added safety.
Ideal for labs that require precision and safety, the AKF-100L Reactor is perfect for a wide range of chemical and pharmaceutical applications.
Explore more: AKF-100L Double-Glazed Reactor
3 notes · View notes