期刊文献+

cDNA末端扩增技术的研究进展 被引量:8

Research progress of rapid amplification of cDNA ends
下载PDF
导出
摘要 cDNA末端扩增技术是一种以PCR反应为基础,快速获得已知cDNA序列3′端和5′端的方法,是克隆全长cDNA序列的主要手段之一。本文从RACE原理出发,对RACE技术3个关键步骤(反转录、TdT加尾、PCR扩增)的优化和改良措施进行了透彻分析,并详细阐述RACE的最新研究进展———“电子”cDNA克隆。 Rapid amplification of cDNA ends is a method obtaining 3' ends and 5' ends of known cDNA fragments based on PCR reaction, and one of the primary means cloning cDNA fragments. Beginning with the principle this article analyses the three critical steps (transcription, TdT tailing, PCR amplification) of RACE technique in detail, and expatiates the latest RACE techniques (Marathon - PCR, SMART - RACE, In silico cloning).
出处 《河北林果研究》 2006年第2期157-161,共5页 Hebei Journal of Forestry and Orchard Research
关键词 RACE 全长CDNA序列 PCR 反转录 RACE full - length cDNA PCR transcription
  • 相关文献

参考文献25

  • 1Frohman M A,Dush M K,Mrtin G R,et al.Rapid production of full-length cDNAs from rare transcripts:amplification using single gene-specific oligonuleotide primer[J].Proc Natl Acad Sci USA,1988,85(23):8998-9002.
  • 2Chomczynski P,Sacchi N.Single step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction[J].Anal Biochem,1987,162:156-159.
  • 3Favaloro J,Treisman R,Kamen R.Transcription maps of polyma virus-specific RNA:analysis by two-dimer-sional nucleas S1 gel mapping[J].Methods Enzymol,1980,65:719-748.
  • 4邢桂春,张成岗,魏汉东,贺福初.采用RACE技术获得全长人新基因MAGE-D1[J].中国生物化学与分子生物学报,2001,17(2):203-208. 被引量:27
  • 5Schaefer B C.Revolutions in rapid amolification of cDNA ends:New strategies for polymerase chain reaction cloning of full-length cDNA ends[J].Anal Biochem,1995,227:255-273.
  • 6Loh E Y,Elliott J F,Cwirla S,et al.Polymerase Chain Reaction with Single-Sided Specificity:Analysis of T Cell Receptor delta Chain[J].Science,1989,243:217-220.
  • 7Templeton N S,Urselay E,Safer B.Reducing artifact and increasing the yield of specific DNA target fragments during PCR-RACE or anchor PCR[J].Bio Techniques,1992,15:48-51.
  • 8Ewards J B D M,Delort J,Mallet J.Oligodeoxyribonucleotide ligation to single-stranded cDNAs:A new tool for cloning 5′ends of mRNA and for contructing cDNA libraries by in vitro amplification[J].Nucleic Acids Res,1991,19(19):5227-5232.
  • 9Troutt A B.Ligation-anchored PCR:A simple amplification technique with single-sided specificity[J].Proc Natl Acad Sci USA,1992,89:9823-9825.
  • 10Liu X W,Gorovsky M A.Mapping the 5′ and 3′ ends of Tetrahymena thermophila mRNA using RNA ligase mediated amplification of cDNA ends (RLM-RACE)[J].Nucleic Acids Res,1993,21(21):4954-4960.

二级参考文献87

  • 1[1]Frohman MA et al.Proc Natl Acad Sci USA,1988:85:8998
  • 2[2]LohEY et al.Science,1989;243:217
  • 3[3]Ohara O et al.Proc NatlAcadSciUSA,1989;86:5673
  • 4[4]Edwards JBDM et al.Nucleic Acids Res,1991; 195227
  • 5[5]Troutt AB et al.Proc Natl Acad Sci USA,1992;899823
  • 6[6]Liu Xet al.Nucleic Acids Res,1993;21:4954
  • 7[7]Apte Aet al.BioTechniques,1993;15:890
  • 8[8]Maruyama Ket al.Gene,1994;138:171
  • 9[9]Schaefer BC.Anal Biochem,1995;227:255
  • 10[10]Templeton NS et al.BioTechniques,1993;15:48

共引文献72

同被引文献114

引证文献8

二级引证文献46

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部