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

Q1 Biochemistry, Genetics and Molecular Biology Biomolecular Detection and Quantification Pub Date : 2016-06-01 DOI:10.1016/j.bdq.2016.02.001
Hua-Jun He , Jamie L. Almeida , Steve P. Lund , Carolyn R. Steffen , Steve Choquette , Kenneth D. Cole
{"title":"Development of NIST standard reference material 2373: Genomic DNA standards for HER2 measurements","authors":"Hua-Jun He ,&nbsp;Jamie L. Almeida ,&nbsp;Steve P. Lund ,&nbsp;Carolyn R. Steffen ,&nbsp;Steve Choquette ,&nbsp;Kenneth D. Cole","doi":"10.1016/j.bdq.2016.02.001","DOIUrl":null,"url":null,"abstract":"<div><p>NIST standard reference material (SRM) 2373 was developed to improve the measurements of the <em>HER2</em> gene amplification in DNA samples. SRM 2373 consists of genomic DNA extracted from five breast cancer cell lines with different amounts of amplification of the <em>HER2</em> gene. The five components are derived from the human cell lines SK-BR-3, MDA-MB-231, MDA-MB-361, MDA-MB-453, and BT-474. The certified values are the ratios of the <em>HER2</em> gene copy numbers to the copy numbers of selected reference genes <em>DCK</em>, <em>EIF5B</em>, <em>RPS27A</em>, and <em>PMM1</em>. The ratios were measured using quantitative polymerase chain reaction and digital PCR, methods that gave similar ratios. The five components of SRM 2373 have certified <em>HER2</em> amplification ratios that range from 1.3 to 17.7. The stability and homogeneity of the reference materials were shown by repeated measurements over a period of several years. SRM 2373 is a well characterized genomic DNA reference material that can be used to improve the confidence of the measurements of <em>HER2</em> gene copy number.</p></div>","PeriodicalId":38073,"journal":{"name":"Biomolecular Detection and Quantification","volume":"8 ","pages":"Pages 1-8"},"PeriodicalIF":0.0000,"publicationDate":"2016-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.bdq.2016.02.001","citationCount":"19","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biomolecular Detection and Quantification","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2214753516300031","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
引用次数: 19

Abstract

NIST standard reference material (SRM) 2373 was developed to improve the measurements of the HER2 gene amplification in DNA samples. SRM 2373 consists of genomic DNA extracted from five breast cancer cell lines with different amounts of amplification of the HER2 gene. The five components are derived from the human cell lines SK-BR-3, MDA-MB-231, MDA-MB-361, MDA-MB-453, and BT-474. The certified values are the ratios of the HER2 gene copy numbers to the copy numbers of selected reference genes DCK, EIF5B, RPS27A, and PMM1. The ratios were measured using quantitative polymerase chain reaction and digital PCR, methods that gave similar ratios. The five components of SRM 2373 have certified HER2 amplification ratios that range from 1.3 to 17.7. The stability and homogeneity of the reference materials were shown by repeated measurements over a period of several years. SRM 2373 is a well characterized genomic DNA reference material that can be used to improve the confidence of the measurements of HER2 gene copy number.

Abstract Image

Abstract Image

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
开发NIST标准参考物质2373:用于HER2测量的基因组DNA标准
开发了NIST标准参比物质(SRM) 2373,以改进DNA样品中HER2基因扩增的测量。SRM 2373由从5种不同HER2基因扩增量的乳腺癌细胞系中提取的基因组DNA组成。这五种成分分别来源于人细胞系SK-BR-3、MDA-MB-231、MDA-MB-361、MDA-MB-453和BT-474。认证值为HER2基因拷贝数与选定内参基因DCK、EIF5B、RPS27A、PMM1拷贝数之比。使用定量聚合酶链反应和数字PCR方法测量比率,方法给出相似的比率。SRM 2373的五种组分具有经认证的HER2扩增比,范围从1.3到17.7。通过数年的反复测量,证明了标准物质的稳定性和均匀性。SRM 2373是一种表征良好的基因组DNA参考物质,可用于提高HER2基因拷贝数测量的置信度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Biomolecular Detection and Quantification
Biomolecular Detection and Quantification Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
14.20
自引率
0.00%
发文量
0
审稿时长
8 weeks
期刊最新文献
Publisher's Note Establishing essential quality criteria for the validation of circular RNAs as biomarkers qPCR data analysis: Better results through iconoclasm Considerations and quality controls when analyzing cell-free tumor DNA Next-generation sequencing of HIV-1 single genome amplicons
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1