| Protocol for mRNA amplification,非常详细的RT-PCR实验过程[Howard Hughes Medical | 点击: 作者:51protocol收集 来源: 时间: 2007-03-19 本站论坛
|
|  | | |
|
2ul |
0.1M DTT |
|
1ul |
RNaseIN (Promega Cat# N2111) |
|
2ul |
10mM dNTP (Pharmacia Cat# 27-2035-02) |
|
2ul |
Superscript II (Gibco BRL Cat# 18064-071) |
42C for 90min in thermal cycler.
From here, follow the procedure of first round amplification for
Second strand synthesis,
DS cDNA cleanup,
In Vitro TRanscription,
and aRNA purification using RNEasy.
Note: when labeling amplified RNA - USE RANDOM HEXAMERS.
上一篇:Isolation of Retroelement from Plant Genomic DNA,PCR法从植物寻找逆转录元件[Univ 下一篇:Yeast Colony PCR 酵母菌落PCR[] 共8页: 上一页 [1] [2] [3] [4] [5] [6] [7] 8 下一页 |