• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

一种用于检测结核分枝杆菌富含GC且低丰度模板的改进型实时PCR检测方法。

An improved, real-time PCR assay for the detection of GC-rich and low abundance templates of Mycobacterium tuberculosis.

作者信息

Grassi Manuela, Volpe Elisabetta, Colizzi Vittorio, Mariani Francesca

机构信息

Institute Neurobiology and Molecular Medicine, Molec. Med. Section, National Research Council, Via del Fosso del Cavaliere, 100, 00133, Rome, Italy.

出版信息

J Microbiol Methods. 2006 Mar;64(3):406-10. doi: 10.1016/j.mimet.2005.05.002. Epub 2005 Jun 24.

DOI:10.1016/j.mimet.2005.05.002
PMID:15979747
Abstract

The detection of low abundance mRNA and/or GC-rich targets is very difficult using real-time PCR, often requiring laborious optimization procedures. This work shows that formamide is a useful PCR additive, increasing the sensitivity and specificity of SYBR Green real-time PCR to detect low abundance mycobacterial RNA from infected samples.

摘要

使用实时聚合酶链反应(PCR)检测低丰度信使核糖核酸(mRNA)和/或富含鸟嘌呤-胞嘧啶(GC)的靶标非常困难,通常需要繁琐的优化程序。这项研究表明,甲酰胺是一种有用的PCR添加剂,可提高SYBR Green实时PCR检测感染样本中低丰度分枝杆菌RNA的灵敏度和特异性。

相似文献

1
An improved, real-time PCR assay for the detection of GC-rich and low abundance templates of Mycobacterium tuberculosis.一种用于检测结核分枝杆菌富含GC且低丰度模板的改进型实时PCR检测方法。
J Microbiol Methods. 2006 Mar;64(3):406-10. doi: 10.1016/j.mimet.2005.05.002. Epub 2005 Jun 24.
2
A one-step SYBR Green I-based product-enhanced reverse transcriptase assay for the quantitation of retroviruses in cell culture supernatants.一种基于SYBR Green I的一步法产品增强型逆转录酶检测方法,用于定量细胞培养上清液中的逆转录病毒。
J Virol Methods. 2009 Mar;156(1-2):1-7. doi: 10.1016/j.jviromet.2008.10.012. Epub 2008 Dec 5.
3
Nuclear and cytoplasmic mRNA quantification by SYBR green based real-time RT-PCR.基于SYBR Green的实时逆转录PCR进行细胞核和细胞质mRNA定量分析。
Methods. 2006 Aug;39(4):356-62. doi: 10.1016/j.ymeth.2006.06.010.
4
[Detection of 85B mRNA in Mycobacterium tuberculosis cultures using the quantitative QRT-PCR (TaqMan) method].[运用定量QRT-PCR(TaqMan)方法检测结核分枝杆菌培养物中的85B mRNA]
Wiad Lek. 2003;56(9-10):419-24.
5
[Comparison of Tosoh TRCRapid M.TB assay by transcription-reverse transcription concerted reaction (TRC) with Roche COBAS AMPLICOR assay by PCR and with culture for detection of Mycobacterium tuberculosis complex].[通过转录-逆转录协同反应(TRC)的东芝TRCRapid M.TB检测法与通过聚合酶链反应(PCR)的罗氏COBAS AMPLICOR检测法以及用于检测结核分枝杆菌复合群的培养法的比较]
Rinsho Byori. 2008 Apr;56(4):277-82.
6
Simultaneous detection of HCV and HIV-1 by SYBR Green real time multiplex RT-PCR technique in plasma samples.采用SYBR Green实时多重逆转录聚合酶链反应技术同时检测血浆样本中的丙型肝炎病毒和1型人类免疫缺陷病毒
Mol Cell Probes. 2006 Jun-Aug;20(3-4):223-9. doi: 10.1016/j.mcp.2005.12.005. Epub 2006 Mar 14.
7
Identification of viable and non-viable Mycobacterium tuberculosis in mouse organs by directed RT-PCR for antigen 85B mRNA.通过针对抗原85B mRNA的定向逆转录聚合酶链反应鉴定小鼠器官中活的和非活的结核分枝杆菌。
Microb Pathog. 2000 Jun;28(6):335-42. doi: 10.1006/mpat.2000.0353.
8
Detection and quantification of infectious hematopoietic necrosis virus in rainbow trout (Oncorhynchus mykiss) by SYBR Green real-time reverse transcriptase-polymerase chain reaction.通过SYBR Green实时逆转录-聚合酶链反应检测和定量虹鳟(Oncorhynchus mykiss)中的传染性造血坏死病毒
J Virol Methods. 2008 Jan;147(1):157-66. doi: 10.1016/j.jviromet.2007.08.026. Epub 2007 Oct 22.
9
T cell receptor BV repertoires using real time PCR: a comparison of SYBR green and a dual-labelled HuTrec fluorescent probe.使用实时PCR分析T细胞受体BV谱系:SYBR Green与双标记HuTrec荧光探针的比较
J Immunol Methods. 2004 Nov;294(1-2):43-52. doi: 10.1016/j.jim.2004.08.015. Epub 2004 Oct 6.
10
Analysis of multiple exon-skipping mRNA splice variants using SYBR Green real-time RT-PCR.使用SYBR Green实时逆转录PCR分析多个外显子跳跃mRNA剪接变体
J Neurosci Methods. 2007 Mar 15;160(2):294-301. doi: 10.1016/j.jneumeth.2006.09.022. Epub 2006 Nov 13.

引用本文的文献

1
Facilitation of Dye-Based Quantitative Real-Time Polymerase Chain Reaction with Poly(ethylene glycol)-Engrafted Graphene Oxide.聚乙二醇接枝氧化石墨烯对基于染料的定量实时聚合酶链反应的促进作用
Nanomaterials (Basel). 2023 Apr 12;13(8):1348. doi: 10.3390/nano13081348.
2
Genome-wide expression profiling of the response to linezolid in Mycobacterium tuberculosis.结核分枝杆菌对线利福平反应的全基因组表达谱分析。
Curr Microbiol. 2012 Jun;64(6):530-8. doi: 10.1007/s00284-012-0104-9. Epub 2012 Mar 3.
3
Microarray analysis of the chelerythrine-induced transcriptome of Mycobacterium tuberculosis.
微阵列分析白屈菜红碱诱导的结核分枝杆菌转录组。
Curr Microbiol. 2011 Apr;62(4):1200-8. doi: 10.1007/s00284-010-9837-5. Epub 2010 Dec 19.
4
Development and experimental validation of a predictive threshold cycle equation for quantification of virulence and marker genes by high-throughput nanoliter-volume PCR on the OpenArray platform.用于在OpenArray平台上通过高通量纳升级PCR对毒力基因和标记基因进行定量的预测性阈值循环方程的开发与实验验证。
Appl Environ Microbiol. 2008 Jun;74(12):3831-8. doi: 10.1128/AEM.02743-07. Epub 2008 Apr 18.
5
Gene expression profiling of human macrophages at late time of infection with Mycobacterium tuberculosis.结核分枝杆菌感染后期人类巨噬细胞的基因表达谱分析
Immunology. 2006 Aug;118(4):449-60. doi: 10.1111/j.1365-2567.2006.02378.x.