Literature DB >> 17121086

Freezing complete polymerase chain reaction master mix reagents for routine molecular diagnostics.

Donna Marie West1, Jason Sawyer.   

Abstract

The potential of storing complete frozen real-time polymerase chain reactions (PCRs) and real-time reverse transcription PCRs (RT-PCRs), which require only thawing and the addition of template nucleic acid before PCR cycling, was examined. Master mixes containing all necessary reagents at working concentration (except template nucleic acid) were aliquoted into single-reaction volumes and stored at -70 degrees C for periods of up to 8 months. Reactions were removed from storage and nucleic acid template was added and amplified using different real-time PCR instruments. Threshold cycle values were used to monitor changes in assay performance after storage. Results for hybridization probe and TaqMan probe assays showed that freezing complete real-time PCR and RT-PCR reaction mixes was possible without deterioration in assay performance. This approach has advantages for routine molecular diagnostics in areas such as convenience, test consistency, quality control, and ease of use by nonspecialist staff.

Mesh:

Substances:

Year:  2006        PMID: 17121086     DOI: 10.1177/104063870601800609

Source DB:  PubMed          Journal:  J Vet Diagn Invest        ISSN: 1040-6387            Impact factor:   1.279


  5 in total

1.  Cost-effective frozen master mix modification of a commercial methicillin-resistant Staphylococcus aureus PCR assay.

Authors:  Erik Munson; Timothy Block; Janet T Voegeli; Jeanne E Hryciuk; Ronald F Schell
Journal:  J Clin Microbiol       Date:  2009-04-22       Impact factor: 5.948

2.  Modifications of commercial toxigenic Clostridium difficile PCR resulting in improved economy and workflow efficiency.

Authors:  Erik Munson; Dorothy Bilbo; Mary Paul; Maureen Napierala; Jeanne E Hryciuk
Journal:  J Clin Microbiol       Date:  2011-03-30       Impact factor: 5.948

3.  Cost-effective modification of a commercial PCR assay for detection of methicillin-resistant or -susceptible Staphylococcus aureus in positive blood cultures.

Authors:  Erik Munson; Timothy Kramme; Anne Culver; Jeanne E Hryciuk; Ronald F Schell
Journal:  J Clin Microbiol       Date:  2010-02-10       Impact factor: 5.948

4.  An Optimized Direct Lysis Gene Expression Microplate Assay and Applications for Disease, Differentiation, and Pharmacological Cell-Based Studies.

Authors:  Neville S Ng; Simon Maksour; Jeremy S Lum; Michelle Newbery; Victoria Shephard; Lezanne Ooi
Journal:  Biosensors (Basel)       Date:  2022-05-26

5.  Optimization of a combined human parechovirus-enterovirus real-time reverse transcription-PCR assay and evaluation of a new parechovirus 3-specific assay for cerebrospinal fluid specimen testing.

Authors:  Suresh B Selvaraju; W Allan Nix; M Steven Oberste; Rangaraj Selvarangan
Journal:  J Clin Microbiol       Date:  2012-11-21       Impact factor: 5.948

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.