Literature DB >> 19377837

Production and certification of NIST Standard Reference Material 2372 Human DNA Quantitation Standard.

Margaret C Kline1, David L Duewer, John C Travis, Melody V Smith, Janette W Redman, Peter M Vallone, Amy E Decker, John M Butler.   

Abstract

Modern highly multiplexed short tandem repeat (STR) assays used by the forensic human-identity community require tight control of the initial amount of sample DNA amplified in the polymerase chain reaction (PCR) process. This, in turn, requires the ability to reproducibly measure the concentration of human DNA, [DNA], in a sample extract. Quantitative PCR (qPCR) techniques can determine the number of intact stretches of DNA of specified nucleotide sequence in an extremely small sample; however, these assays must be calibrated with DNA extracts of well-characterized and stable composition. By 2004, studies coordinated by or reported to the National Institute of Standards and Technology (NIST) indicated that a well-characterized, stable human DNA quantitation certified reference material (CRM) could help the forensic community reduce within- and among-laboratory quantitation variability. To ensure that the stability of such a quantitation standard can be monitored and that, if and when required, equivalent replacement materials can be prepared, a measurement of some stable quantity directly related to [DNA] is required. Using a long-established conventional relationship linking optical density (properly designated as decadic attenuance) at 260 nm with [DNA] in aqueous solution, NIST Standard Reference Material (SRM) 2372 Human DNA Quantitation Standard was issued in October 2007. This SRM consists of three quite different DNA extracts: a single-source male, a multiple-source female, and a mixture of male and female sources. All three SRM components have very similar optical densities, and thus very similar conventional [DNA]. The materials perform very similarly in several widely used gender-neutral assays, demonstrating that the combination of appropriate preparation methods and metrologically sound spectrophotometric measurements enables the preparation and certification of quantitation [DNA] standards that are both maintainable and of practical utility.

Entities:  

Mesh:

Substances:

Year:  2009        PMID: 19377837     DOI: 10.1007/s00216-009-2782-0

Source DB:  PubMed          Journal:  Anal Bioanal Chem        ISSN: 1618-2642            Impact factor:   4.142


  12 in total

1.  Quantification of plasmid DNA standards for U.S. EPA fecal indicator bacteria qPCR methods by droplet digital PCR analysis.

Authors:  Mano Sivaganesan; Manju Varma; Shawn Siefring; Richard Haugland
Journal:  J Microbiol Methods       Date:  2018-07-11       Impact factor: 2.363

2.  Development of a Vero cell DNA reference standard for residual DNA measurement in China.

Authors:  Shouchun Cao; Guanmu Dong; Jianrong Tang; Jia Li; Jinghua Liu; Leitai Shi; Changgui Li; Junzhi Wang
Journal:  Hum Vaccin Immunother       Date:  2013-01-04       Impact factor: 3.452

3.  Evaluating Digital PCR for the Quantification of Human Genomic DNA: Accessible Amplifiable Targets.

Authors:  Margaret C Kline; Erica L Romsos; David L Duewer
Journal:  Anal Chem       Date:  2016-01-25       Impact factor: 6.986

4.  Nuclear, chloroplast, and mitochondrial data of a US cannabis DNA database.

Authors:  Rachel Houston; Matthew Birck; Bobby LaRue; Sheree Hughes-Stamm; David Gangitano
Journal:  Int J Legal Med       Date:  2018-02-20       Impact factor: 2.686

5.  Evaluation of a 13-loci STR multiplex system for Cannabis sativa genetic identification.

Authors:  Rachel Houston; Matthew Birck; Sheree Hughes-Stamm; David Gangitano
Journal:  Int J Legal Med       Date:  2015-12-10       Impact factor: 2.686

Review 6.  U.S. initiatives to strengthen forensic science & international standards in forensic DNA.

Authors:  John M Butler
Journal:  Forensic Sci Int Genet       Date:  2015-06-30       Impact factor: 4.882

7.  Development of a reference standard of Escherichia coli DNA for residual DNA determination in China.

Authors:  Lan Wang; Chunming Rao; Kai Gao; Yonghong Li; Zhihao Fu; Hua Bi; Junzhi Wang
Journal:  PLoS One       Date:  2013-09-25       Impact factor: 3.240

8.  Evaluation of microbial qPCR workflows using engineered Saccharomyces cerevisiae.

Authors:  S M Da Silva; L K Vang; N D Olson; S P Lund; A S Downey; Z Kelman; M L Salit; N J Lin; J B Morrow
Journal:  Biomol Detect Quantif       Date:  2016-02-19

9.  Development of NIST standard reference material 2373: Genomic DNA standards for HER2 measurements.

Authors:  Hua-Jun He; Jamie L Almeida; Steve P Lund; Carolyn R Steffen; Steve Choquette; Kenneth D Cole
Journal:  Biomol Detect Quantif       Date:  2016-03-09

10.  Quantification of plasmid DNA reference materials for Shiga toxin-producing Escherichia coli based on UV, HR-ICP-MS and digital PCR.

Authors:  Wen Liang; Li Xu; Zhiwei Sui; Yan Li; Lanying Li; Yanli Wen; Chunhua Li; Shuzhen Ren; Gang Liu
Journal:  Chem Cent J       Date:  2016-09-12       Impact factor: 4.215

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.