• 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

Formalin-induced infidelity in PCR-amplified DNA fragments.

作者信息

De Giorgi C, Finetti Sialer M, Lamberti F

机构信息

Istituto di Nematologia Agraria, Consiglio Nazionale delle Ricerche, Bari, Italy.

出版信息

Mol Cell Probes. 1994 Dec;8(6):459-62. doi: 10.1006/mcpr.1994.1065.

DOI:10.1006/mcpr.1994.1065
PMID:7700266
Abstract

A 643-nucleotide-long fragment of rDNA gene was amplified by PCR in the nematode worm Caenorhabditis elegans. When the experiments were performed by using samples fixed in formalin, artefacts were detected. While the size of the amplified fragment resulted unaffected, very striking differences were seen in the nucleotide sequences of the amplified fragments. Furthermore, in many cases, the PCR reaction failed completely. The results obtained might warn of potential problems, especially when the amount of DNA to be amplified is scarce.

摘要

相似文献

1
Formalin-induced infidelity in PCR-amplified DNA fragments.
Mol Cell Probes. 1994 Dec;8(6):459-62. doi: 10.1006/mcpr.1994.1065.
2
Caenorhabditis elegans as a model system for mtDNA replication defects.秀丽隐杆线虫作为 mtDNA 复制缺陷的模型系统。
Methods. 2010 Aug;51(4):437-43. doi: 10.1016/j.ymeth.2010.03.003. Epub 2010 Mar 15.
3
Discrimination of primer 3'-nucleotide mismatch by taq DNA polymerase during polymerase chain reaction.聚合酶链反应过程中Taq DNA聚合酶对引物3' -核苷酸错配的识别
Anal Biochem. 2000 Aug 15;284(1):11-8. doi: 10.1006/abio.2000.4635.
4
Development of a new PCR protocol for the detection of species and genotypes (strains) of Echinococcus in formalin-fixed, paraffin-embedded tissues.开发一种用于检测福尔马林固定、石蜡包埋组织中棘球蚴物种和基因型(菌株)的新型聚合酶链反应方案。
Int J Parasitol. 2008 Jul;38(8-9):1065-71. doi: 10.1016/j.ijpara.2007.11.008. Epub 2007 Dec 4.
5
Polymerase chain reaction/sequencing analysis of ras mutations in paraffin-embedded tissues as compared with 3T3 transfection and polymerase chain reaction/sequencing of frozen tumor deoxyribonucleic acids.石蜡包埋组织中ras突变的聚合酶链反应/测序分析与3T3转染及冷冻肿瘤脱氧核糖核酸的聚合酶链反应/测序的比较
Lab Invest. 1992 Apr;66(4):504-11.
6
Rapid and reliable protocol for direct sequencing of material amplified by the polymerase chain reaction.用于对聚合酶链反应扩增产物进行直接测序的快速可靠方案。
Biotechniques. 1990 Jul;9(1):66-8, 70, 72.
7
Sampling the genomic pool of protein tyrosine kinase genes using the polymerase chain reaction with genomic DNA.利用聚合酶链反应和基因组DNA对蛋白质酪氨酸激酶基因的基因组文库进行采样。
Biochem Biophys Res Commun. 1998 Aug 28;249(3):660-7. doi: 10.1006/bbrc.1998.9003.
8
Large fragment Bst DNA polymerase for whole genome amplification of DNA from formalin-fixed paraffin-embedded tissues.用于从福尔马林固定石蜡包埋组织中进行DNA全基因组扩增的大片段Bst DNA聚合酶。
BMC Genomics. 2006 Dec 12;7:312. doi: 10.1186/1471-2164-7-312.
9
Detection of immunoglobulin gene rearrangement of B cell non-Hodgkin's lymphomas and leukemias in fresh, unfixed and formalin-fixed, paraffin-embedded tissue by polymerase chain reaction.通过聚合酶链反应检测新鲜、未固定以及福尔马林固定、石蜡包埋组织中B细胞非霍奇金淋巴瘤和白血病的免疫球蛋白基因重排
Lab Invest. 1993 Jun;68(6):746-57.
10
Genomic characterization of Tv-ant-1, a Caenorhabditis elegans tag-61 homologue from the parasitic nematode Trichostrongylus vitrinus.来自寄生线虫玻璃细颈线虫的秀丽隐杆线虫tag-61同源物Tv-ant-1的基因组特征分析。
Gene. 2007 Aug 1;397(1-2):12-25. doi: 10.1016/j.gene.2007.03.011. Epub 2007 Mar 30.

引用本文的文献

1
Update on Molecular Diagnosis in Extranodal NK/T-Cell Lymphoma and Its Role in the Era of Personalized Medicine.结外NK/T细胞淋巴瘤分子诊断的最新进展及其在精准医学时代的作用
Diagnostics (Basel). 2022 Feb 5;12(2):409. doi: 10.3390/diagnostics12020409.
2
Probing the active fraction of soil microbiomes using BONCAT-FACS.利用 BONCAT-FACS 探测土壤微生物组的活性组分。
Nat Commun. 2019 Jun 24;10(1):2770. doi: 10.1038/s41467-019-10542-0.
3
Methanol-based fixation is superior to buffered formalin for next-generation sequencing of DNA from clinical cancer samples.
对于临床癌症样本DNA的下一代测序,基于甲醇的固定方法优于缓冲福尔马林。
Ann Oncol. 2016 Mar;27(3):532-9. doi: 10.1093/annonc/mdv613. Epub 2015 Dec 17.
4
gbpA as a Novel qPCR Target for the Species-Specific Detection of Vibrio cholerae O1, O139, Non-O1/Non-O139 in Environmental, Stool, and Historical Continuous Plankton Recorder Samples.将gbpA作为实时定量聚合酶链反应(qPCR)的新型靶标,用于在环境样本、粪便样本及历史连续浮游生物记录器样本中对霍乱弧菌O1群、O139群、非O1/非O139群进行特异性检测。
PLoS One. 2015 Apr 27;10(4):e0123983. doi: 10.1371/journal.pone.0123983. eCollection 2015.
5
Long-term effects of ocean warming on the prokaryotic community: evidence from the vibrios.海洋变暖对原核生物群落的长期影响:弧菌的证据。
ISME J. 2012 Jan;6(1):21-30. doi: 10.1038/ismej.2011.89. Epub 2011 Jul 14.
6
Accuracy of BRCA1 and BRCA2 founder mutation analysis in formalin-fixed and paraffin-embedded (FFPE) tissue.福尔马林固定石蜡包埋(FFPE)组织中BRCA1和BRCA2始祖突变分析的准确性
Fam Cancer. 2006;5(4):337-42. doi: 10.1007/s10689-006-0003-y. Epub 2006 May 25.
7
Flow sorting of microorganisms for molecular analysis.用于分子分析的微生物流式分选
Appl Environ Microbiol. 1997 Nov;63(11):4223-31. doi: 10.1128/aem.63.11.4223-4231.1997.