#RealTimePCR

[cytgen]

Abstract The analysis of nucleotide sequences of the Argemone genus samples by bioinformatics methods was aimed at the study of phylogenetic relationships of species within the genus, at the development of genus-specific primer pairs, and TaqMan-probe and their verification in silico. Molecular genetic studies by the polymerase chain reaction method in the “real-time” mode (RT-PCR) were devoted to checking the “performance” and specificity of the developed system of primers and TaqMan-probe using samples of eight species of Argemone and 11 species of other plants. Phylogenetic analysis using internal transcribed spacer 1 (ITS1) sequences confirmed previous phylogenetic studies and improved understanding of relationships within the genus. Before the in vitro test of the developed system of primers and TaqMan-probe, the ability of the extracted DNA to be amplified by the RT-PCR method using the system of primers and the TaqMan-probe to the 18S rRNA gene of eukaryotes was checked to exclude pseudo-negative results during the further verification of specificity. The conditions for RT-PCR were selected, namely, temperatures and times of denaturation, hybridization, elongation, and the number of cycles. The developed system of primers and TaqMan-probe for the RT-PCR method demonstrated high species specificity and sensitivity. Amplification was noted only in DNA samples of eight Argemone species, while PCR analysis of other plant species and negative controls showed no amplification. The detection limit of the developed system was determined to be 0.01%. It is proposed that this marker system be used to detect falsification in food and other products, particularly Argemone contamination in mustard or coconut oil.

[marialabtro]

Real Time PCR LT-PCR402

Labtro Real-Time PCR features high-quality linearized temperature control, modular thermal cycling, and 2 fluorescence detection channels. With dual-channel reagent detection, RS-232 connectivity, and a compact A4 size, it is ideal for precise, portable, on-site inspections.

[athenese-dx]

𝗔𝘁𝗵𝗲𝗻𝗲𝘀𝗲-𝗗𝘅'𝘀 𝗠𝗼𝗹𝗲𝗰𝘂𝗹𝗮𝗿 𝗗𝗶𝗮𝗴𝗻𝗼𝘀𝘁𝗶𝗰 𝗥𝗮𝗻𝗴𝗲𝘀!

Athenese-Dx MolDx ranges are engineered for precision, accuracy, and reliability. Our comprehensive suite includes:

1. DNA/RNA Extraction Kits – High-yield & pure nucleic acid extraction 2. Nucleic Acid Extractor – Automated, fast, and efficient workflow

𝗥𝗲𝗮𝗹-𝗧𝗶𝗺𝗲 𝗣𝗖𝗥 𝗞𝗶𝘁𝘀:

1. HBV & HCV (Quantitative) – Accurate viral load detection 2. Typhoid & Leptospira (Qualitative) – Rapid & reliable pathogen identification

Watch the video to learn more.

Visit → https://athenesedx.com/product-category/molecular-pcr-kits/

AtheneseDx #PCRKits #MolecularDiagnostics #IVD #India #PCR #RealTimePCR #NewProductLaunch #LaboratoryExcellence #DiagnosticSolutions #Diagnostics #Pathology #Medical #Medicine #Practitioner #ClinicalDiagnostics #ClinicalChemistry #ELISA #RapidTest #ClinicalLaboratory #RTPCR #Healthcare #InVitroDiagnostics #LabSupplies #LaboratorySupplies #DiagnosticKits

[pathologylab]

On #World_AIDS_Day, we're proud to introduce the #HIV-Q Real-Time RT-PCR #Kit. This advanced test detects and quantifies HIV-1 #RNA with high sensitivity and specificity, ensuring precise diagnostics for healthcare professionals. Compatible with most real-time #PCR instruments, it offers reliable, cross-reactivity-free results to support better patient outcomes.

Let’s join hands in the fight against HIV with innovative #solutions!

#WorldAIDSDay2024 #HIVTesting #DiagnosticsInnovation #RealTimePCR #HealthcareInnovation #Diagnostics #Genes2Me #g2m #awareness

[globalinsightblog]

PCR Renaissance: Driving Innovation in Molecular Diagnostics

The Polymerase Chain Reaction (PCR) market is experiencing a renaissance driven by breakthrough technologies, expanding applications, and the increasing demand for precise molecular diagnostics.

As the cornerstone of modern molecular biology, PCR continues to evolve, offering new possibilities in disease detection, genetic analysis, and personalized medicine. Over the next decade, this market is poised for substantial growth as advancements in PCR platforms, including digital PCR, real-time PCR, and multiplex PCR, enable researchers and clinicians to unlock deeper insights into the molecular mechanisms underlying health and disease.

Innovations in PCR technology are revolutionizing the field of molecular diagnostics, with a focus on enhancing sensitivity, specificity, and multiplexing capabilities. From infectious disease testing and oncology biomarker analysis to prenatal screening and forensic DNA profiling, PCR is driving advancements across diverse clinical and research domains. Moreover, the integration of artificial intelligence and machine learning algorithms into PCR data analysis is facilitating faster and more accurate interpretation of results, leading to improved diagnostic accuracy and more informed clinical decision-making.

#PCR #MolecularDiagnostics #PrecisionMedicine #GeneticAnalysis #HealthcareInnovation #DigitalPCR #RealTimePCR #MultiplexPCR #AIinHealthcare #MachineLearning #InfectiousDisease #Oncology #ForensicScience #PersonalizedMedicine #BiomedicalResearch

[seanzim]

Excited to be a part of the help Thermo Fisher Scientific is providing to this pandemic. I actually got to create the user interfaces used on the latest real-time PCR units that are being used to find results to tests: The Applied Biosystsem’s QuantStudio 3 and 5 instruments.

[hurtworld]

mesaj attım ama cevap vermedin dostum. PCR ve qPCR teknikleriyle alakalı kaynak olarak yardımcı olabilir misin?

mendeley kullanıyor musun bilmiyorum ama ben APA şeklinde buraya atayım kaynakları sen seç beğen al dostum.

Polymerase chain reaction - Wikipedia. (n.d.). Retrieved May 27, 2020, from https://en.wikipedia.org/wiki/Polymerase_chain_reaction

Citations for Chemical Breakthrough Awards 2017 Awardees. (n.d.). Division of the History of Chemistry. Retrieved May 27, 2020, from http://www.scs.illinois.edu/~mainzv/HIST/awards/CCB-2017_Awardees.php

Kary B. Mullis – Nobel Lecture: The Polymerase Chain Reaction. (n.d.). Retrieved May 27, 2020, from http://nobelprize.org/nobel_prizes/chemistry/laureates/1993/mullis-lecture.html

Advice on How to Survive the Taq Wars. (2006). GEN Genetic Engineering News – Biobusiness Channel, 26(9). https://www.genengnews.com/magazine/49/advice-on-how-to-survive-the-taq-wars/

Babineaux, M. J., & Alter, M. J. (2011). Viral Hepatitis. In Netter’s Infectious Disease (pp. 399–410). Elsevier Inc. https://doi.org/10.1016/B978-1-4377-0126-5.00067-7

Key ingredient in coronavirus tests comes from Yellowstone’s lakes. (2020). Science. https://www.nationalgeographic.com/science/2020/03/key-ingredient-in-coronavirus-tests-comes-from-yellowstone/

Bing, D., Boles, C., Rehman, F., Audeh, M., Belmarsh, M., Kelley, B., & Adams, C. (1996). Bridge amplification: a solid phase PCR system for the amplification and detection of allelic differences in single copy genes. Genetic Identity Conference Proceedings, Seventh International Symposium on Human Identification. http://www.promega.com/geneticidproc/ussymp7proc/0726.html

Tomar, R. S. (2010). Molecular markers & plant biotechnology. New India Pub. Agency.

Full Text – LaNe RAGE: a new tool for genomic DNA flanking sequence determination. (n.d.). Retrieved May 27, 2020, from http://www.ejbiotechnology.info/content/vol8/issue2/full/7/index.html

Kieleczawa, J. (2006). DNA sequencing II : optimizing preparation and cleanup. Jones and Bartlett Publishers.

David, F. (2002). Utiliser les propriétés topologiques de l’ADN: une nouvelle arme contre les agents pathogènes. Fusion. http://www.lab-rech-associatives.com/pdf/Utiliser la Topologie de l’ADN.pdf

Kellogg, D. E., Rybalkin, I., Chen, S., Mukhamedova, N., Vlasik, T., Siebert, P. D., & Chenchik, A. (1994). TaqStart antibody(TM): “Hot start” PCR facilitated by a neutralizing monoclonal antibody directed against Taq DNA polymerase. BioTechniques, 16(6), 1134–1137.

Ochman, H., Gerber, A. S., & Hartl, D. L. (1988). Genetic applications of an inverse polymerase chain reaction. Genetics, 120(3), 621–623.

Ninfa, A. B. et all. (2010). Fundamental laboratory Approaches for Biochemistry and Biotechnology about PAGE. In Fundamental laboratory Approaches for Biochemistry and Biotechnology. John Wiley & Sons. inc.

Boehnke, M., Arnheim, N., Li, H., & Collins, F. S. (1989). Fine-structure genetic mapping of human chromosomes using the polymerase chain reaction on single sperm: Experimental design considerations. American Journal of Human Genetics, 45(1), 21–32.

Coronavirus: il viaggio dei test. (n.d.). Istituto Superiore Di Sanità. Retrieved May 27, 2020, from https://www.iss.it/web/guest/primo-piano/-/asset_publisher/o4oGR9qmvUz9/content/id/5269706

Patidar, M., Agrawal, S., Parveen, F., & Khare, P. (2015). Molecular insights of saliva in solving paternity dispute. Journal of Forensic Dental Sciences, 7(1), 76. https://doi.org/10.4103/0975-1475.150325

Chemical Synthesis, Sequencing, and Amplification of DNA (class notes on MBB/BIO 343). (n.d.). Arizona State University. Retrieved May 27, 2020, from http://photoscience.la.asu.edu/photosyn/courses/BIO_343/lecture/DNAtech.html

Electronic PCR. (n.d.). NCBI – National Center for Biotechnology Information. Retrieved May 27, 2020, from https://www.ncbi.nlm.nih.gov/sutils/e-pcr/

Bogetto, P. and W. L. (2000). Helpful tips for PCR. Focus, 22(1), 12. http://tools.thermofisher.com/Content/Focus/Focus Volume 22 Issue 1.pdf

Mullis, K. B. (1990). The unusual origin of the polymerase chain reaction. Scientific American, 262(4), 56–65. https://doi.org/10.1038/scientificamerican0490-56

Borman, J., Schuster, D., Li, W., Jessee, J., & Rashtchian, A. (2000). PCR from problematic templates. Focus, 22(1), 10. http://tools.thermofisher.com/Content/Focus/Focus Volume 22 Issue 1.pdf

Mullis, K. B. (1998). Dancing naked in the mind field. Pantheon Books. https://archive.org/details/dancingnakedinmi00mull

PCR. (n.d.). Genetic Science Learning Center, University of Utah. Retrieved May 27, 2020, from http://learn.genetics.utah.edu/content/labs/pcr/

Polymerase Chain Reaction (PCR). (n.d.). National Center for Biotechnology Information, U.S. National Library of Medicine. Retrieved May 27, 2020, from https://www.ncbi.nlm.nih.gov/probe/docs/techpcr/

Rabinow, P. (1996). Making PCR : a story of biotechnology. University of Chicago Press. https://archive.org/details/makingpcrstoryof00rabi

Park, D. J. (2005). A new 5′ terminal murine GAPDH exon identified using 5′RACE LaNe. Molecular Biotechnology, 29(1), 39–46. https://doi.org/10.1385/MB:29:1:39

White, B. A. (1993). PCR protocols : current methods and applications. Humana Press.

Myrick, K. V., & Gelbart, W. M. (2002). Universal Fast Walking for direct and versatile determination of flanking sequence. Gene, 284(1–2), 125–131. https://doi.org/10.1016/S0378-1119(02)00384-0

McPherson, M. J., & Møller, S. G. (2006). PCR. Taylor & Francis.

Bagchi, D. (2013). Bio-nanotechnology : a revolution in food, biomedical, and health sciences. Wiley-Blackwell.

Liu, Y. G., & Whittier, R. F. (1995). Thermal asymmetric interlaced PCR: automatable amplification and sequencing of insert end fragments from P1 and YAC clones for chromosome walking. Genomics, 25(3), 674–681. https://doi.org/10.1016/0888-7543(95)80010-J

Thornhill, A. (2007). Single Cell Diagnostics. Cell, 132. https://doi.org/10.1007/978-1-59745-298-4

Khan, Z., Poetter, K., & Park, D. J. (2008). Enhanced solid phase PCR: mechanisms to increase priming by solid support primers. Analytical Biochemistry, 375(2), 391–393. https://doi.org/10.1016/j.ab.2008.01.021

Baron, S. (1996). Medical microbiology (4th ed.). University of Texas Medical Branch at Galveston. https://www.ncbi.nlm.nih.gov/books/NBK7813/

Bustin, S. A., & Nolan, T. (2009). Analysis of mRNA Expression by Real-time. In Real-Time PCR: Current Technology and Applications. Caister Academic Press. http://www.caister.com/realtimepcr

White, B. A., Shyamala, V., & Ames, G. F.-L. (2003). Single Specific Primer-Polymerase Chain Reaction (SSP-PCR) and Genome Walking. In PCR Protocols (pp. 339–348). Humana Press. https://doi.org/10.1385/0-89603-244-2:339

Dobosy, J. R., Rose, S. D., Beltz, K. R., Rupp, S. M., Powers, K. M., Behlke, M. A., & Walder, J. A. (2011). RNase H-dependent PCR (rhPCR): Improved specificity and single nucleotide polymorphism detection using blocked cleavable primers. BMC Biotechnology, 11, 80. https://doi.org/10.1186/1472-6750-11-80

Sambrook, J., & Russell, D. W. (David W. (2001). Molecular cloning : a laboratory manual (3rd ed.). Cold Spring Harbor Laboratory Press. https://archive.org/details/molecularcloning0000samb_p7p5

David, F., & Turlotte, É. (1998). Une methode d’amplification genique isotherme. Comptes Rendus de l’Academie Des Sciences - Serie III, 321(11), 909–914. https://doi.org/10.1016/S0764-4469(99)80005-5

Shen, C., & Zhang, Z. (2013). An Overview of Nanoparticle-Assisted Polymerase Chain Reaction Technology. In Bio-Nanotechnology: A Revolution in Food, Biomedical and Health Sciences (pp. 97–106). Blackwell Publishing Ltd. https://doi.org/10.1002/9781118451915.ch5

Kleppe, K., Ohtsuka, E., Kleppe, R., Molineux, I., & Khorana, H. G. (1971). Studies on polynucleotides. XCVI. Repair replication of short synthetic DNA’s as catalyzed by DNA polymerases. Journal of Molecular Biology, 56(2), 341–361. https://doi.org/10.1016/0022-2836(71)90469-4

Park, D. J. (2004). 3′ RACE LaNe: A simple and rapid fully nested PCR method to determine 3′-terminal cDNA sequence. BioTechniques, 36(4), 586–590. https://doi.org/10.2144/04364bm04

Kim, B., Kim, J., Kim, M., Kim, B.-D., Jo, S., Park, S., Son, J., Hwang, S., Dugasani, S., Chang, I., Kim, M., & Liu, W. (2016). Ternary and senary representations using DNA double-crossover tiles. Nanotechnology, 10(45), 105601. https://doi.org/10.1088/0957-4484

Isenbarger, T. A., Finney, M., Ríos-Velázquez, C., Handelsman, J., & Ruvkun, G. (2008). Miniprimer PCR, a new lens for viewing the microbial world. Applied and Environmental Microbiology, 74(3), 840–849. https://doi.org/10.1128/AEM.01933-07

Raoult, D., Aboudharam, G., Crubézy, E., Larrouy, G., Ludes, B., & Drancourt, M. (2000). Molecular identification by “suicide PCR” of Yersinia pestis as the agent of Medieval Black Death. Proceedings of the National Academy of Sciences of the United States of America, 97(23), 12800–12803. https://doi.org/10.1073/pnas.220225197

Herman, J. G., Graff, J. R., Myöhänen, S., Nelkin, B. D., & Baylin, S. B. (1996). Methylation-specific PCR: A novel PCR assay for methylation status of CpG islands. Proceedings of the National Academy of Sciences of the United States of America, 93(18), 9821–9826. https://doi.org/10.1073/pnas.93.18.9821

Zietkiewicz, E., Rafalski, A., & Labuda, D. (1994). Genome fingerprinting by simple sequence repeat (SSR)-anchored polymerase chain reaction amplification. Genomics, 20(2), 176–183. https://doi.org/10.1006/geno.1994.1151

San Millán, R. M., Martínez-Ballesteros, I., Rementeria, A., Garaizar, J., & Bikandi, J. (2013). Online exercise for the design and simulation of PCR and PCR-RFLP experiments. BMC Research Notes, 6(1), 513. https://doi.org/10.1186/1756-0500-6-513

Horton, R. M., Hunt, H. D., Ho, S. N., Pullen, J. K., & Pease, L. R. (1989). Engineering hybrid genes without the use of restriction enzymes: gene splicing by overlap extension. Gene, 77(1), 61–68. https://doi.org/10.1016/0378-1119(89)90359-4

Schwartz, J. J., Lee, C., & Shendure, J. (2012). Accurate gene synthesis with tag-directed retrieval of sequence-verified DNA molecules. Nature Methods, 9(9), 913–915. https://doi.org/10.1038/nmeth.2137

Mueller, P. R., & Wold, B. (1989). In vivo footprinting of a muscle specific enhancer by ligation mediated PCR. Science, 246(4931), 780–786. https://doi.org/10.1126/science.2814500

Priye, A., Hassan, Y. A., & Ugaz, V. M. (2013). Microscale chaotic advection enables robust convective DNA replication. Analytical Chemistry, 85(21), 10536–10541. https://doi.org/10.1021/ac402611s

Vincent, M., Xu, Y., & Kong, H. (2004). Helicase-dependent isothermal DNA amplification. EMBO Reports, 5(8), 795–800. https://doi.org/10.1038/sj.embor.7400200

Pierce, K. E., & Wangh, L. J. (2007). Linear-After-The-Exponential Polymerase Chain Reaction and Allied Technologies (pp. 65–85). https://doi.org/10.1007/978-1-59745-298-4_7

Krishnan, M., Ugaz, V. M., & Burns, M. A. (2002). PCR in a Rayleigh-Bénard convection cell. Science, 298(5594), 793. https://doi.org/10.1126/science.298.5594.793

Innis, M. A., Myambo, K. B., Gelfand, D. H., & Brow, M. A. D. (1988). DNA sequencing with Thermus aquaticus DNA polymerase and direct sequencing of polymerase chain reaction-amplified DNA. Proceedings of the National Academy of Sciences of the United States of America, 85(24), 9436–9440. https://doi.org/10.1073/pnas.85.24.9436

Stemmer, W. P. C., Crameri, A., Ha, K. D., Brennan, T. M., & Heyneker, H. L. (1995). Single-step assembly of a gene and entire plasmid from large numbers of oligodeoxyribonucleotides. Gene, 164(1), 49–53. https://doi.org/10.1016/0378-1119(95)00511-4

Alonso, A., Martín, P., Albarrán, C., García, P., García, O., Fernández De Simón, L., García-Hirschfeld, J., Sancho, M., De La Rúa, C., & Fernández-Piqueras, J. (2004). Real-time PCR designs to estimate nuclear and mitochondrial DNA copy number in forensic and ancient DNA studies. Forensic Science International, 139(2–3), 141–149. https://doi.org/10.1016/j.forsciint.2003.10.008

Yeh, S. H., & Mink, C. A. M. (2012). Bordetella pertussis and Pertussis (Whooping Cough). In Netter’s Infectious Disease (pp. 11–14). Elsevier Inc. https://doi.org/10.1016/B978-1-4377-0126-5.00003-3

Kwok, S., Mack, D. H., Mullis, K. B., Poiesz, B., Ehrlich, G., Blair, D., Friedman-Kien, A., & Sninsky, J. J. (1987). Identification of human immunodeficiency virus sequences by using in vitro enzymatic amplification and oligomer cleavage detection. Journal of Virology, 61(5), 1690–1694. https://doi.org/10.1128/jvi.61.5.1690-1694.1987

Cai, H. Y., Caswell, J. L., & Prescott, J. F. (2014). Nonculture Molecular Techniques for Diagnosis of Bacterial Disease in Animals: A Diagnostic Laboratory Perspective. In Veterinary Pathology (Vol. 51, Issue 2, pp. 341–350). https://doi.org/10.1177/0300985813511132

Bustin, S. A., Benes, V., Garson, J. A., Hellemans, J., Huggett, J., Kubista, M., Mueller, R., Nolan, T., Pfaffl, M. W., Shipley, G. L., Vandesompele, J., & Wittwer, C. T. (2009). The MIQE guidelines: Minimum information for publication of quantitative real-time PCR experiments. Clinical Chemistry, 55(4), 611–622. https://doi.org/10.1373/clinchem.2008.112797

Quill, E. (2008). Medicine: Bood-matching goes genetic. In Science (Vol. 319, Issue 5869, pp. 1478–1479). https://doi.org/10.1126/science.319.5869.1478

Garibyan, L., & Avashia, N. (2013). Polymerase chain reaction. Journal of Investigative Dermatology, 133(3), 1–4. https://doi.org/10.1038/jid.2013.1

Movert, E., Wu, Y., Lambeau, G., Kahn, F., Touqui, L., & Areschoug, T. (2013). Using Patient Pathways to Accelerate the Drive to Ending Tuberculosis. Journal of Infectious Diseases, 208(12), 2025–2035. https://doi.org/10.1093/INFDIS

Lawyer, F. C., Stoffel, S., Saiki, R. K., Chang, S. Y., Landre, P. A., Abramson, R. D., & Gelfand, D. H. (1993). High-level expression, purification, and enzymatic characterization of full-length Thermus aquaticus DNA polymerase and a truncated form deficient in 5′ to 3′ exonuclease activity. Genome Research, 2(4), 275–287. https://doi.org/10.1101/gr.2.4.275

Pombert, J. F., Sistek, V., Boissinot, M., & Frenette, M. (2009). Evolutionary relationships among salivarius streptococci as inferred from multilocus phylogenies based on 16S rRNA-encoding, recA, secA, and secY gene sequences. BMC Microbiology, 9, 232. https://doi.org/10.1186/1471-2180-9-232

Chien, A., Edgar, D. B., & Trela, J. M. (1976). Deoxyribonucleic acid polymerase from the extreme thermophile Thermus aquaticus. Journal of Bacteriology, 127(3), 1550–1557. https://doi.org/10.1128/jb.127.3.1550-1557.1976

Sharkey, D. J., Scalice, E. R., Christy, K. G., Atwood, S. M., & Daiss, J. L. (1994). Antibodies as thermolabile switches: High temperature triggering for the polymerase chain reaction. Bio/Technology, 12(5), 506–509. https://doi.org/10.1038/nbt0594-506

Carr, A. C., & Moore, S. D. (2012). Robust quantification of polymerase chain reactions using global fitting. PLoS ONE, 7(5), e37640. https://doi.org/10.1371/journal.pone.0037640

Rhizobium, G. E. (2013). Complete Genome Sequence of the Sesbania Symbiont and Rice. Nucleic Acids Research, 1(1256879), 13–14. https://doi.org/10.1093/nar

Pavlov, A. R., Pavlova, N. V., Kozyavkin, S. A., & Slesarev, A. I. (2004). Recent developments in the optimization of thermostable DNA polymerases for efficient applications. In Trends in Biotechnology (Vol. 22, Issue 5, pp. 253–260). https://doi.org/10.1016/j.tibtech.2004.02.011

Determining Annealing Temperatures for Polymerase Chain Reaction. (2012). The American Biology Teacher, 74(4), 256–260. https://doi.org/10.1525/abt.2012.74.4.9

Cheng, S., Fockler, C., Barnes, W. M., & Higuchi, R. (1994). Effective amplification of long targets from cloned inserts and human genomic DNA. Proceedings of the National Academy of Sciences of the United States of America, 91(12), 5695–5699. https://doi.org/10.1073/pnas.91.12.5695

Saiki, R., Gelfand, D., Stoffel, S., Scharf, S., Higuchi, R., Horn, G., Mullis, K., & Erlich, H. (1988). Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase. Science, 239(4839), 487–491. https://doi.org/10.1126/science.239.4839.487

Saiki, R. K., Scharf, S., Faloona, F., Mullis, K. B., Horn, G. T., Erlich, H. A., & Arnheim, N. (1985). Enzymatic amplification of β-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia. Science, 230(4732), 1350–1354. https://doi.org/10.1126/science.2999980

[kenhangiang]

TRI TÔN 🔴 Trong ngày 15-8, trên địa bàn huyện phát hiện thêm 6 trường hợp mắc COVID-19 (đã có kết quả xét nghiệm RealtimePCR dương tính với SARS-CoV-2). Tri Tôn đẩy mạnh tầm soát, phát hiện trường hợp nhiễm COVID-19 trong...

[theworldthroughthemindeye]

AIDS and its Virus.

AIDS or Acquired Immuno Deficiency Syndrome is a disease that is troubling this world for more than 3 decades since it’s discovery in 1981. More than 20.9 million people are inflicted by the disease as reported by WHO in mid-2017. The disease is caused by a Virus named Human Immuno Deficiency Virus, which attacks our immune system making us vulnerable to diseases. AIDS patients suffer from a…

[marialabtro]

Real Time PCR System LT-RPS301

Labtro advanced real-time PCR system uses long-lasting LED technology for reliable results with ±0.2℃ accuracy and uniformity. It minimizes multi-color crosstalk, eliminates ROX correction, and reduces reagent use with its new optical scanning detection system.

[athenese-dx]

We're excited to launch our latest innovation in molecular diagnostics. Our new real-time PCR kits are designed to deliver precise and reliable results for your laboratory needs.

To explore the full details of our real-time PCR kits, visit → https://athenesedx.com/product-category/molecular-pcr-kits/

To Buy → https://store.athenesedx.com/product-category/molecular-pcr-kits/

AtheneseDx #IVD #India #PCR #PCRKits #MolecularDiagnostics #Innovation #RealTimePCR #NewProductLaunch #LaboratoryExcellence #DiagnosticSolutions #Diagnostics #Pathology #Medical #Medicine #Practitioner #ClinicalDiagnostics #ClinicalChemistry #ELISA #RapidTest #ClinicalLaboratory #RTPCR #Healthcare #InVitroDiagnostics #LabSupplies #LaboratorySupplies #DiagnosticKits

[pathologylab]

comprehensive #HPV detection with #G2M's cutting-edge HPV-Q Real-Time PCR kit. Our multiplex diagnostic kits qualitatively detect the #DNA of 28 types of HPV in human specimens, including 14 low, medium, and 14 high-risk HPV strains. Utilizing specific primers and fluorescent-labeled probes, our kit ensures precise identification and accurate #results.

Visit our website for more information https://www.genes2me.com/ivd-real-time-pcr-test-kits/human-papilloma-virus-detection-kit

For more details, Call us at +91-8800821778 or drop us an email at social@genes2me.com

#Genes2Me #Humanpapillomavirus #RealTimePCR #ViralDetection #Comprehensive #CervicalCancer #HPVVirus #MolecularDiagnostics #Kits #rtpcr #ivd #solutions #pcr #detection

[seanzim]

Here's a video of how Thermo Fisher Scientific is helping with #Covid19 on a global scale. And, on that note, I've had the privilege of leading the visuals for 2 of the 4 instruments talked about. Super honored to work here and actually see our products making a difference in the world.

[marialabtro]

Real Time PCR System LT-RPS401

Labtro advanced real-time PCR system offers rapid heating (6.1°C/s) and cooling (5.0°C/s) with ±0.1°C uniformity. It features a 10.4-inch LCD touchscreen, efficient temperature control, and a high-brightness, long-life, maintenance-free LED light source for reliable results.

[marialabtro]

Real Time PCR System LT-RPS401

Labtro advanced real-time PCR system offers rapid heating (6.1°C/s) and cooling (5.0°C/s) with ±0.1°C uniformity. It features a 10.4-inch LCD touchscreen, efficient temperature control, and a high-brightness, long-life, maintenance-free LED light source for reliable results.

[marialabtro]

Real Time PCR System LT-RPS301

Labtro advanced real-time PCR system uses long-lasting LED technology for reliable results with ±0.2℃ accuracy and uniformity. It minimizes multi-color crosstalk, eliminates ROX correction, and reduces reagent use with its new optical scanning detection system.