Literature DB >> 20810770

Impact of long-term storage on stability of standard DNA for nucleic acid-based methods.

Barbara Röder1, Karin Frühwirth, Claus Vogl, Martin Wagner, Peter Rossmanith.   

Abstract

Real-time PCR is dependent upon a calibration function for quantification. While long-term storage of standards saves cost and time, solutions of DNA are prone to degradation. We present here the benchmark treatment for preservation of DNA standards, involving storage in 50% glycerol-double-distilled water, whereby a deviation of 0.2 threshold cycle (C(T)) values resulted after 100 days of storage.

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Year:  2010        PMID: 20810770      PMCID: PMC3020885          DOI: 10.1128/JCM.01230-10

Source DB:  PubMed          Journal:  J Clin Microbiol        ISSN: 0095-1137            Impact factor:   5.948


  20 in total

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5.  Shear-induced assembly of lambda-phage DNA.

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9.  Evaluation of degradation pathways for plasmid DNA in pharmaceutical formulations via accelerated stability studies.

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Journal:  J Food Prot       Date:  2004-08       Impact factor: 2.077

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  16 in total

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9.  Effect of pre-analytic variables on the reproducibility of qPCR relative telomere length measurement.

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10.  Ensuring the Safety and Security of Frozen Lung Cancer Tissue Collections through the Encapsulation of Dried DNA.

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