丁香实验_LOGO
登录
提问
我要登录
|免费注册
点赞
收藏
wx-share
分享

反向PCR

互联网

1851

 

主要内容如下:

         RT-PCR

         Competitive and Quantative RT-PCR

         In Situ RT-PCR

         RL-PCR

         DNA Contamination

         RT-PCR FAQ


RT-PCR

         RT-PCR Protocol (UMBC)
First strand synthesis and subsequent PCR amplification. Based on LTI protocol

         Reverse Transcriptase PCR (NWFSC)
Procedure for cDNA synthesis on dynabeads oligo(dT)25

         RT-PCR (Cause's  Lab)
Detailed protocol for RT and PCR

         RT-PCR (Lazo Lab)
First strand cDNA synthesis and PCR amplification

         RT-PCR
Procedure either for RT-PCR and primer extension. For primer extension, just add hot dATP 

         cDNA Synthesis and Amplification of POLY(A) mRNA by RT-PCR (Immunology Resource)
CDNA synthesis from mRNA and subsequent PCR amplification 

         Nested RT-PCR From Paraffin Section (Hans Popper)
This protocol is for the non-isotopic detection of hepatitis C RNA and albumin mRNA (as an internal control) from 4 micron sections of formalin-fixed, paraffin-embedded liver biopsies by RT-PCR. The procedure for RNA extraction from formalin fixed paraffin embedded section and PCR amplification is described. 

Competitive and Quantative RT-PCR

 

         Competitive Quantitative RT-PCR (PDF) (Ambion)
Detailed protocol for competitive quantitative RT-PCR

         Semi-Quantitative RT-PCR (Mike A. Dyer)
From RNA isolation, reverse transcription to PCR...

         RT In Situ PCR (Gerard J. Nuovo)
RT in situ PCR allows for the routine and rapid detection of low copy viral and human RNAs. Success with RT in situ PCR is best accomplished with formalin fixed, paraffin embedded material, which allows the study of archival material.

         In Situ RT-PCR (HYBAID)
Detailed Step-by-step protocol  

         In Situ PCR On Plant Tissues (Bo Johansen)
Provides detailed protocol on tissue preparation, in situ PCR, detection and required reagents.

RL-PCR

         Reverse Ligation Mediated RT-PCR (Antisense Research Group)
RL-PCR can be broken down into a number of simple steps. Synthesis by in vitro transcription and purification of an RNA linker species. Extraction of total RNA from cells into which oligodeoxynucleotide has been delivered by, for example, streptolysin O permeabilization. Ligation of the RNA linker to all available 5' monophosphates in the purified total cellular RNA sample. Reverse Transcription of the RNA using a gene - specific primer. Amplification of specific fragments by PCR using linker - specific and gene - specific primers. Sub- amplification of the first PCR product using linker specific and nested, labelled, gene specific primers. 

RT-PCR FAQ

提问
扫一扫
丁香实验小程序二维码
实验小助手
丁香实验公众号二维码
关注公众号
反馈
TOP
打开小程序