网站地图本站论坛
高级搜索收藏本站
当前位置:试验方案>核酸试验>PCR> 正文
  • Long-PCR Reagents and Guidelines 长距离PCR反应溶液和方法指导[USDA]

  • 点击:    作者:51protocol收集   来源: 日期:2007-03-19    本站论坛
(2). G/C-rich 3' ends may be too sticky and give non-specific products. Using this additional rule primer length might increase to 25 or 26 bases. We have not yet used this rule in our primer-picking but we are experimenting.

REFERENCES

1. Cheng, S., Fockler, C., Barnes, W., Higuchi, R. Effective amplification of long targets from cloned inserts and human genomic DNA. Proc. Natl. Acad. Sci. 91, 5695-5699 (1994).

2. Crameri, A. and Stemmer, W. 10^20-Fold aptamer library amplification without gel purification. Nucleic Acids Research 21, 4410 (1993)


上一篇:RT-PCR 反转录生产cDNA链以及PCR扩增[Yale University]   下一篇:RAPD PCR Colony Miniprep

共2页: 上一页 [1] 2 下一页

推荐文章
·PCR产物克隆
·RT-PCR反应体系的优化
·PCR与RT-PCR技术
·RT-PCR实验方法大全
·RT-PCR (Reverse transcription PCR)
·Two Step REAL TIME RT-PCR PROTOCOL
·RT-PCR简介
·引物设计软件oligo应用简介
·PCR引物设计的黄金法则
·PCR产物的克隆
·PCR的基本原理
·The Polymerase Chain Reaction (PCR)
·Real-Time PCR 与Traditional PCR比较
·PCR[polymerase chain reaction]技术总论
·Primer Design:Manual and Automated Prime
·引物的稀释和使用
相关文章
·RT-PCR 反转录生产cDNA链以及PCR扩增[Yale
·RAPD PCR Colony Miniprep
·RT-PCR Analysis 详细的RT-PCR方法[Harvard
·Degenerate PCR 简并PCR,包括引物设计、反
·RT-PCR Protocol[University of Chicago]
·M. hyopneumoniae PCR [Iowa State Univers
·PCR Protocol(per Adam 08/12/04)[Universi
·"BEST" PCR 从质粒上扩增DNA的PCR条件[Carn
·Protocol for Enhancing PCR of Very Diffi
·Yeast Colony PCR 酵母菌落PCR[]
·Protocol for mRNA amplification,非常详
·Isolation of Retroelement from Plant Gen
·Expand High Fidelity PCR,高保真PCR扩增
·Polymerase Chain Reaction (PCR),热启动P
·Disruption by Fusion PCR[Upstate Medical
·Crude Extract Prep for In Vitro Spindle
·Real time PCR-ABI Prism 7000[MIT]
·RT-PCR Protocol
·PCR Protocol(per Adam 08/12/04) 【Univer
推荐专题

↑返回顶部   打印本页   关闭窗口↓  
 本站申明 联系我们 网站地图
Copyright© 试验方案

Powered by DedeCms email:htmyth#yahoo.com.cn

Optimized to 1024x768 to Firefox,Opera and MS-IE6