Relevant bibliographies by topics / Real-time QPCR

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Real-time QPCR'

Author: Grafiati
Published: 4 June 2021
Last updated: 25 July 2025

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Journal articles on the topic "Real-time QPCR"

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Zhu, Tianyu, Xin Liu, and Xinqing Xiao. "Physical Simulation-Based Calibration for Quantitative Real-Time PCR." Applied Sciences 14, no. 12 (2024): 5031. http://dx.doi.org/10.3390/app14125031.

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The fluorescence quantitative polymerase chain reaction (qPCR) instrument has been widely used in molecular biology applications, where the reliability of the qPCR performance directly affects the accuracy of its detection results. In this paper, an integrated, physics-based calibration device was developed to improve the accuracy and reliability of qPCR, realizing the calibration of qPCR instruments’ standard curve through physical simulations. With this calibration device, the collected temperature was used as the control signal to alter the fluorescence output, which allowed different probe
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Nybo, Kristie. "Real-Time qPCR/qRT-PCR Methods: Standard Curves." BioTechniques 48, no. 1 (2010): 31–33. http://dx.doi.org/10.2144/000113340.

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Baskarathevan, J., R. K. Taylor, W. Ho, R. L. McDougal, R. G. Shivas, and B. J. R. Alexander. "Real-Time PCR Assays for the Detection of Puccinia psidii." Plant Disease 100, no. 3 (2016): 617–24. http://dx.doi.org/10.1094/pdis-08-15-0851-re.

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Puccinia psidii (Myrtle rust) is an emerging pathogen that has a wide host range in the Myrtaceae family; it continues to show an increase in geographic range and is considered to be a significant threat to Myrtaceae plants worldwide. In this study, we describe the development and validation of three novel real-time polymerase reaction (qPCR) assays using ribosomal DNA and β-tubulin gene sequences to detect P. psidii. All qPCR assays were able to detect P. psidii DNA extracted from urediniospores and from infected plants, including asymptomatic leaf tissues. Depending on the gene target, qPCR
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Lv, Zhongquan, Mingxin Zhang, Hui Zhang, and Xinxin Lu. "Utility of Real-Time Quantitative Polymerase Chain Reaction in DetectingMycobacterium tuberculosis." BioMed Research International 2017 (2017): 1–5. http://dx.doi.org/10.1155/2017/1058579.

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This study aimed to assess the value of real-time quantitative polymerase chain reaction (RT-qPCR) for the detection ofMycobacterium tuberculosis(MTB). Samples from 192 patients with suspected MTB were examined by RT-qPCR and an improved Löwenstein–Jensen (L-J) culture method. To evaluate the diagnostic usefulness of RT-qPCR in detecting MTB, a receiver operating characteristic (ROC) curve for RT-qPCR was generated, and the area under the curve (AUC) as well as a cutoff value was calculated. Using the L-J culture method as the gold standard, accuracy of the RT-qPCR method for detecting MTB was
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CHENG, CHORNG-MING, TARA DORAN, WEN LIN, KAI-SHUN CHEN, DONNA WILLIAMS-HILL, and RUIQING PAMBOUKIAN. "Interlaboratory Validation for a Real-Time PCR Salmonella Detection Method Using the ABI 7500 FAST Real-Time PCR System." Journal of Food Protection 78, no. 6 (2015): 1119–24. http://dx.doi.org/10.4315/0362-028x.jfp-14-244.

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Sixteen FERN (Food Emergency Response Network) member laboratories collaborated in this study to verify extension of the real-time PCR Salmonella detection method originally designed for the single-tube Cepheid SmartCycler II and validated against the Salmonella method of the U.S. Food and Drug Administration Bacteriological Analytical Manual to the Applied Biosystems (ABI) 7500 FAST Real-Time PCR system multiwell plate platform. Four foods were selected for this study: chili powder, soft cheese, fish, and tomatoes; these foods represent products that are commonly analyzed for the presence of
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Knapp, Jenny, Séverine Lallemand, Franck Monnien, et al. "Real-time multiplex PCR for human echinococcosis and differential diagnosis." Parasite 30 (2023): 3. http://dx.doi.org/10.1051/parasite/2023003.

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Molecular identification of rare human infectious pathogens appears to be one of the most relevant current methods for rapid diagnosis and management of patients. PCR techniques, in particular real-time quantitative PCR, are best suited for the detection of DNA from the pathogens, even at low concentrations. Echinococcosis infections are due to helminths of the Echinococcus genus, with closely related species involved in parasitic lesions affecting animals and, accidentally, humans. We developed a multiplex qPCR (MLX qPCR) assay allowing for the detection of four Echinococcus species involved
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de Boer, M. E., D. Roelofs, and N. M. van Straalen. "Real-time RT-QPCR integration in soil quality assessment." Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology 154, no. 1 (2009): S16. http://dx.doi.org/10.1016/j.cbpa.2009.05.059.

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Johnson, Christopher E., Amritha Premasuthan, Jessica Satkoski Trask, and Sree Kanthaswamy. "Species Identification ofCannabis sativaUsing Real-Time Quantitative PCR (qPCR),." Journal of Forensic Sciences 58, no. 2 (2013): 486–90. http://dx.doi.org/10.1111/1556-4029.12055.

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Witvrouwen, Isabel, Andreas B. Gevaert, Emeline M. Van Craenenbroeck, and Amaryllis H. Van Craenenbroeck. "MicroRNA Isolation from Plasma for Real-Time qPCR Array." Current Protocols in Human Genetics 99, no. 1 (2018): e69. http://dx.doi.org/10.1002/cphg.69.

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FONSECA JUNIOR, Antônio Augusto, Carolina Kymie Vasquez NONAKA, Estefânia de Oliveira GUEDES, et al. "Detection of agents associated with respiratory diseases of swine by real time PCR." Revista Brasileira de Saúde e Produção Animal 16, no. 2 (2015): 300–307. http://dx.doi.org/10.1590/s1519-99402015000200005.

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Porcine Respiratory Disease Complex (PRDC) is a group of diseases that cause high losses in the swine industry. Several infectious agents are related to PRDC including porcine circovirus 2 (PCV-2), pseudorabies virus (SuHV-1),Haemophilus parasuis (HP), Mycoplasma hypneumoniae (MH) and Pasteurela multocida (PM). The aim of this study was to develop real-time PCRs (qPCR) for the detection of these infectious agents. Oligonucleotides were designed for each specific infectious agent and labeled with different fluorophores to amplify specific parts of the genome. This was done in two groups of reac
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Dissertations / Theses on the topic "Real-time QPCR"

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Allen, Charlotte Annette. "Cytokine detection in EIAV-infected equine monocyte-derived macrophages using quantitative real-time polymerase chain reaction." Thesis, Texas A&M University, 2007. http://hdl.handle.net/1969.1/85887.

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The replication of equine infectious anemia virus (EIAV) in macrophages not only leads to cell death, but also to the induction of a variety of cytokines that may affect immune function. Cytokine production may be responsible for the fever, anorexia, hemorrhages, lethargy or thrombocytopenia seen in the acute and chronic phases of equine infectious anemia (EIA). The study of the equine immune system and inflammatory responses, by measuring cytokine expression, can provide important insight into disease pathogenesis in the horse. We have extended studies of virulent and avirulent EIAV clones by
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Pettersson, Erik. "Investigation of tissue factor mRNA levels in human platelets using real-time PCR." Thesis, Uppsala universitet, Institutionen för medicinsk biokemi och mikrobiologi, 2012. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-180831.

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Tissue factor (TF), a 47 kDa glycoprotein, is the initiator of the extrinsic pathway of blood coagulation and consequently of the upmost importance when damage to blood vessel occurs. The source of TF in circulation has been investigated. However, the source of TF is still not clear. One theory is that platelets express and increases the expression of TF after stimulation and the aim of our report was to investigate whether platelets really are a source for TF in circulation. Using specific primers for TF mRNA, platelets in plasma from healthy volunteers and from patients suffering from cardia
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Patil, Neeraj. "Detection of Sclerotinia sclerotiorum using qPCR assay and comparison between three qPCR systems to check sensitivity." Thesis, Högskolan i Skövde, Institutionen för biovetenskap, 2021. http://urn.kb.se/resolve?urn=urn:nbn:se:his:diva-20265.

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Sclerotinia sclerotiorum is a pathogenic fungus that infects around 400 species of host    plants. Stem rot disease caused by this fungus is economically disastrous for Brassica napus cultivators in Sweden. Due to the lack of disease resistant cultivars, disease management has been solely dependent on fungicide application. The current disease  prediction models are not scientifically accurate and take into account factors such as   weather, previous disease incidence, and conomic effects which often result in unnecessary and excessive use of fungicides by cultivators. Real-Time Polymerase Cha
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Nayak, Arun Kumar. "Stability and quantitative surveillance of Helicobacter pylori and Campylobacter jejuni in environmental waters by real time qPCR." Diss., Connect to online resource - MSU authorized users, 2008.

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Amiri, Mehdi. "Real-time PCR detection and PFGE typing of Pseudomonas aeruginosa from cystic fibrosis patients." Doctoral thesis, Università Politecnica delle Marche, 2016. http://hdl.handle.net/11566/243098.

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Pseudomonas aeruginosa (PA) infection is the main cause of mortality in Cystic Fibrosis (CF) patients. Rapid and sensitive PA detection is pivotal to improve the prognosis. This thesis includes two parts. The first focuses on the development of a Real-time PCR protocol to detect dormant- non-culturable PA in sputum samples from CF patients (CFPA). 12 culture-positive (CP) and 29 culture-negative (CN) samples were analyzed by a qPCR targeting ecfX, 24% resulted positive (P), with bacterial counts (102 - 106 cells/ml) also higher than those obtained for CP samples. A significant association of c
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Sharif, Sanaz. "Comparison of real-time PCR assays for screening of meticillin-resistant Staphylococcus aureus." Thesis, Uppsala universitet, Institutionen för medicinsk biokemi och mikrobiologi, 2011. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-154460.

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Staphylococcus aureus belongs to the normal flora. Many healthy people are colonized by the bacterium mainly in the nose but also on the skin and on other mucous membranes without showing symptoms. After damage to the skin, the bacterium can enter the wound and cause infections. Methicillin-resistant S. aureus (MRSA) is resistant to b-lactam antibiotics such as penicillin and methicillin. The gene that gives resistance characteristic of MRSA is the mecA-gene. MRSA strains are spread in both hospitals and in the community, and it is important to identify these bacteria with rapid and sensitive
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Muradrasoli, Shaman. "Detection and Quantification of Variable Viral RNA by Real-Time PCR Assays." Doctoral thesis, Uppsala universitet, Klinisk virologi, 2008. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-9193.

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As the area of nucleic acid based technologies develops, so will our understanding of how structural variations in DNA and RNA pathogens are associated with disease. The overall goal of this thesis is the development of broadly targeted measurement techniques for variable viral RNA by Real-Time PCR (here referred to as quantitative reverse transcriptase PCR, QRT-PCR). In papers I & II, broadly targeted and specific QRT-PCRs were used to study expression of endogenous and exogenous betaretrovirus sequences in human tissues. Results from human tissues demonstrated endogenous betaretrovirus e
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Cao, Cong Yuan. "Real-time qPCR and metagenomics for studying filamentous bulking in full-scale and lab-scale activated sludge treatment systems." Thesis, University of Macau, 2015. http://umaclib3.umac.mo/record=b3335494.

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ALBUQUERQUE, Yvana Maria Maia de. "Reação em cadeia da polimerase em tempo real quantitativa (QPCR) para diagnóstico da tuberculos pulmonar em escarro de pacientes com HIV/aids." Universidade Federal de Pernambuco, 2012. https://repositorio.ufpe.br/handle/123456789/18503.

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Submitted by Caroline Falcao (caroline.rfalcao@ufpe.br) on 2017-04-06T16:49:28Z No. of bitstreams: 2 license_rdf: 1232 bytes, checksum: 66e71c371cc565284e70f40736c94386 (MD5) 2012-tese-YvanaMariaMaiaAlbuquerque.pdf: 1555304 bytes, checksum: ce271c42fa04e7796e60750e627bc8d8 (MD5)<br>Made available in DSpace on 2017-04-06T16:49:28Z (GMT). No. of bitstreams: 2 license_rdf: 1232 bytes, checksum: 66e71c371cc565284e70f40736c94386 (MD5) 2012-tese-YvanaMariaMaiaAlbuquerque.pdf: 1555304 bytes, checksum: ce271c42fa04e7796e60750e627bc8d8 (MD5) Previous issue date: 2012-05-25<br>O diagnóstico da tube
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Pinto, Alessandro. "Real-time aptapcr: a novel approach exploiting nucleic acid aptamers for ultrasensitive detection of analytes for clinical diagnostic and in food analysis." Doctoral thesis, Universitat Rovira i Virgili, 2012. http://hdl.handle.net/10803/80744.

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The thesis aimed to develop and characterize a novel detection approach, which we termed aptaPCR exploiting nucleic acid aptamers as combined recognition and reporter biocomponents for the ultrasensitive detection of analytes. Nucleic acid aptamers are synthetic ligands selected from vast combinatorial libraries through a process referred to as SELEX – Systematic Evolution of Ligand By Exponential Enrichment. As compared to other natural and synthetic receptor, aptamers possess unique chemical and biochemical characteristics, such as: a well known chemistry, remarkable stability, an abi
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Books on the topic "Real-time QPCR"

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Taberlet, Pierre, Aurélie Bonin, Lucie Zinger, and Eric Coissac. Single-species detection. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780198767220.003.0009.

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Chapter 9 “Single-species detection” deals with the practical aspects of detecting a single and predefined taxon with eDNA, with a particular focus on the use of quantitative PCR (qPCR) for this purpose. After presenting how single-species detection has been implemented in a few seminal studies, it details the principles underlying qPCR. More specifically, it describes the typical qPCR amplification curve and the different systems (SYBR green and TaqMan probe assays) available to record amplicon accumulation in real time via fluorescence measurements. Chapter 9 also explains how the initial nu
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Book chapters on the topic "Real-time QPCR"

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Chen, Caifu, Ruoying Tan, Linda Wong, Richard Fekete, and Jason Halsey. "Quantitation of MicroRNAs by Real-Time RT-qPCR." In Methods in Molecular Biology. Humana Press, 2010. http://dx.doi.org/10.1007/978-1-60761-944-4_8.

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Wang, Wei, Katja Scheffler, Ying Esbensen, and Lars Eide. "Quantification of DNA Damage by Real-Time qPCR." In Methods in Molecular Biology. Springer New York, 2016. http://dx.doi.org/10.1007/978-1-4939-3040-1_3.

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Bifeld, Eugenia. "Quantification of Intracellular Leishmania spp. Using Real-Time Quantitative PCR (qPCR)." In Methods in Molecular Biology. Springer New York, 2019. http://dx.doi.org/10.1007/978-1-4939-9210-2_13.

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Lech, Maciej, and Hans-Joachim Anders. "Expression Profiling by Real-Time Quantitative Polymerase Chain Reaction (RT-qPCR)." In Methods in Molecular Biology. Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4939-0882-0_13.

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Trindade, Gisela Freitas, Sheila Maria Barbosa de Lima, Constança Britto, and Alice Gomes Fernandes-Monteiro. "Detection of Yellow Fever Virus by Quantitative Real-Time PCR (qPCR)." In Methods in Molecular Biology. Springer New York, 2019. http://dx.doi.org/10.1007/978-1-4939-9833-3_6.

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Farhana, Wani, Nulevino Iralu, Sumiah Wani, Dasari Meghanath, and Aflaq Hamid. "Real-Time PCR (qPCR) for Plant Virus Detection and Expression Analysis." In Springer Protocols Handbooks. Springer US, 2025. https://doi.org/10.1007/978-1-0716-4390-7_23.

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Lewis, April M., and Kelly C. Rice. "Quantitative Real-Time PCR (qPCR) Workflow for Analyzing Staphylococcus aureus Gene Expression." In Methods in Molecular Biology. Springer New York, 2014. http://dx.doi.org/10.1007/7651_2014_193.

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Busi, Florent. "Fluorescent Oligonucleotide Probes for the Quantification of RNA by Real-Time qPCR." In Methods in Molecular Biology. Springer US, 2020. http://dx.doi.org/10.1007/978-1-0716-0278-2_18.

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Elfving, Betina. "Investigation of Synaptic Vesicle Proteins in Rat Brain Tissue Using Real-Time qPCR." In Methods in Molecular Biology. Springer US, 2022. http://dx.doi.org/10.1007/978-1-0716-1916-2_5.

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Stoddard, Robyn Anne. "Detection of Pathogenic Leptospira spp. Through Real-Time PCR (qPCR) Targeting the LipL32 Gene." In PCR Detection of Microbial Pathogens. Humana Press, 2012. http://dx.doi.org/10.1007/978-1-60327-353-4_17.

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Conference papers on the topic "Real-time QPCR"

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Lin, Xueju, Neil Sharma, and Crystal Lee. "Development and Validation of In-Field qPCR Methods for Water Microbial Analysis at Oil and Gas Facilities." In CORROSION 2015. NACE International, 2015. https://doi.org/10.5006/c2015-05948.

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Abstract Quantitative real-time polymerase chain reaction (qPCR) is a highly sensitive method for the quantification of microorganisms in natural and engineered environments such as oil and gas facilities. This study developed in-field methods for sample processing and nucleic acid extraction from water samples, the design and validation of qPCR assays targeting Domains Bacteria and Archaea, and 3 physiological groups (iron-reducing bacteria, sulfate-reducing microorganisms (SRM), and methanogens) of corrosion-causing microorganisms. A novel, field-friendly method was successful for use in iso
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Zhu, Xiang Y., Alvin Ayala, Hetal Modi, and John J. Kilbane. "Application of Quantitative, Real-Time PCR in Monitoring Microbiologically-Influenced Corrosion (MIC) in Gas Pipelines." In CORROSION 2005. NACE International, 2005. https://doi.org/10.5006/c2005-05493.

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Abstract Quantitative PCR (qPCR) methods (fluorogenic 5′-nuclease assay and SYBR Green I assay) were developed to detect and quantify bacteria and some critical sub-populations related to gas and oil pipeline corrosion. 16S rRNA genes were targeted for the detection and quantification of total bacteria using fluorogenic 5′-nuclease assays. The functional genes, dissimilatory sulfite reductase gene (dsrAB), nitrite reductase gene (nirS), and methyl-coenzyme M reductase gene (mcrA), were targeted for sulfate reducing bacteria (SRB), denitrifying bacteria, and methanognes, respectively. The metho
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Hutcherson, Justin, and Mark Reed. "On Site qPCR Application for Rapid Microbial Detection and Quantification." In CORROSION 2020. NACE International, 2020. https://doi.org/10.5006/c2020-14600.

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Abstract Microbial contamination is a major concern in oil/gas system or industrial water operation where it can result in multiple major corrosion issues and efficiency losses. Chemical treatment is the primary means to control microbial contamination, but due to changes in temperature and water sources, this results in major shifts in the microbial levels and populations which can influence the efficacy of these treatments. Due to the shifts in the number of bacteria and the change in the dominant microbial species, optimal dosage of biocide is very difficult. Inadequate dosage regimen will
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Yim, Priscilla, Jennifer Berkman, Cora Woo, and Junko Stevens. "Abstract 4978: Rapid and sensitive detection of oncoviruses using a simplified real-time RT-qPCR system." In Proceedings: AACR 102nd Annual Meeting 2011‐‐ Apr 2‐6, 2011; Orlando, FL. American Association for Cancer Research, 2011. http://dx.doi.org/10.1158/1538-7445.am2011-4978.

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Andavolu, Radhika G., Dennis M. Frisman, Arnold H. Rodriguez, Shinger Shu, and Murthy VS Andavolu. "Abstract C168: Oligo GEArray®: Validation of gene expression data by Real‐Time™ qPCR and immunohistochemistry." In Abstracts: AACR-NCI-EORTC International Conference: Molecular Targets and Cancer Therapeutics--Nov 15-19, 2009; Boston, MA. American Association for Cancer Research, 2009. http://dx.doi.org/10.1158/1535-7163.targ-09-c168.

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Na, Young-Soon, Young Soo Park, Min-Hee Ryu, et al. "Abstract B211: Comparison of detection ofFGFR2amplification by quantitative real-time-PCR (qPCR) and fluorescentin situhybridization (FISH) in gastric cancer." In Abstracts: AACR-NCI-EORTC International Conference: Molecular Targets and Cancer Therapeutics--Oct 19-23, 2013; Boston, MA. American Association for Cancer Research, 2013. http://dx.doi.org/10.1158/1535-7163.targ-13-b211.

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Kahane, D. "140. Evaluation of Airborne Sampling and Analysis Data by Quantitative Real-Time PCR (QPCR): Its Implications for the Industrial Hygienist." In AIHce 2004. AIHA, 2004. http://dx.doi.org/10.3320/1.2758111.

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Silva, LM, LR Riane, MS Silvério, F. Pittella, and OS Pereira Junior. "DESENVOLVIMENTO DE REAGENTE DE EXTRAÇÃO RÁPIDA DE ÁCIDOS NUCLEICOS E VALIDAÇÃO NA DETECÇÃO DE SARS-COV-2 POR RT-QPCR." In Resumos do 54º Congresso Brasileiro de Patologia Clínica/Medicina Laboratorial. Zeppelini Editorial e Comunicação, 2022. http://dx.doi.org/10.5327/1516-3180.140s1.6930.

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Objetivo: O padrão-ouro no diagnóstico da Covid-19 é o RT-qPCR. Embora seja uma técnica sensível, requer conjuntos caros de reagentes, disponibilidade de equipamentos e tempo para processar as amostras. Além disso, existem etapas suscetíveis a erros que podem prejudicar o diagnóstico, como a extração de ácido ribonucleico (RNA), que demanda tempo e é propensa à contaminação. Diante disso, desenvolvemos um reagente de extração rápida de ácidos nucleicos e comparamos com o método de extração por coluna (PureLink RNA Mini Kit, Invitrogen). Método: O desenvolvimento do reagente envolveu testes de
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Bell, Katherine, Dana Gaffney, Gabriela Martinez, Suso Platero, and Jayaprakash Karkera. "Abstract 3174: A real-time qPCR approach to detect fusions between the KIF5B and RET genes in non-small cell lung cancer." In Proceedings: AACR 104th Annual Meeting 2013; Apr 6-10, 2013; Washington, DC. American Association for Cancer Research, 2013. http://dx.doi.org/10.1158/1538-7445.am2013-3174.

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Saparinjuk, Anastasia, Ralf Birkenhäger, Christoph Becker, and Andreas Knopf. "Vergleichende Genexpressionsanalyse in Pleomorphen Adenomen, Karzinomen ex Pleomporphen Adenomen und Warthin-Tumoren von Hypoxiegenen mittels relativer Quantifizierung mithilfe von Real time-qPCR." In 94. Jahresversammlung Deutsche Gesellschaft für Hals-Nasen-Ohren-Heilkunde, Kopf- und Hals-Chirurgie e.V., Bonn. Georg Thieme Verlag, 2023. http://dx.doi.org/10.1055/s-0043-1766665.

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Reports on the topic "Real-time QPCR"

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Black, Jonathan. Quantitative Real-Time Polymerase Chain Reaction (qPCR) of Filamentous Fungi in Carpet. RTI Press, 2009. http://dx.doi.org/10.3768/rtipress.2009.mr.0011.0909.

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Harris, D. L. Hank, Isabel Turney Harris, James S. Dickson, Stephen Gaul, Brad T. Bosworth, and Lori Feldmann. Quantitative Real-time PCR (qPCR) for the Determination of Salmonella Levels in Lairage. Iowa State University, 2009. http://dx.doi.org/10.31274/ans_air-180814-1009.

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Seroussi, Eyal, and George Liu. Genome-Wide Association Study of Copy Number Variation and QTL for Economic Traits in Holstein Cattle. United States Department of Agriculture, 2010. http://dx.doi.org/10.32747/2010.7593397.bard.

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Copy number variation (CNV) has been recently identified in human and other mammalian genomes and increasing awareness that CNV might be a major source for heritable variation in complex traits has emerged. Despite this, little has been published on CNVs in Holsteins. In order to fill this knowledge-gap, we proposed a genome-wide association study between quantitative trait loci (QTL) for economic traits and CNV in the Holstein cattle. The approved feasibility study was aimed at the genome-wide characterization of CNVs in Holstein cattle and at the demonstrating of their possible association w
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Burns, Malcom, and Gavin Nixon. Literature review on analytical methods for the detection of precision bred products. Food Standards Agency, 2023. http://dx.doi.org/10.46756/sci.fsa.ney927.

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The Genetic Technology (Precision Breeding) Act (England) aims to develop a science-based process for the regulation and authorisation of precision bred organisms (PBOs). PBOs are created by genetic technologies but exhibit changes which could have occurred through traditional processes. This current review, commissioned by the Food Standards Agency (FSA), aims to clarify existing terminologies, explore viable methods for the detection, identification, and quantification of products of precision breeding techniques, address and identify potential solutions to the analytical challenges presente
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