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- 详细信息
- 文献和实验
- 技术资料
- 保存条件:
<- 20℃
- 保质期:
>2 years
- 英文名:
Friendbio Science & Technology Co.,Ltd.
- 库存:
200
- 供应商:
福因德科技(武汉)有限公司
- 规格:
20μg
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文献和实验The traditional method for combating RNases in enzymatic reactions such as in vitro transcription, reverse transcription and translation is to use human placental ribonuclease inhibitor (also known as RNase Inhibitor Protein, RI or hPRI
Human FastTrack mRNA Isolation
. Modified FastTrack 2.0 Protocol Isolation of mRNA 1.Add 15ml of Lysis Buffer (15ml Stock Buffer + 300 ul RNase/Protein Degrader) to the frozen pellet. 2.The tissue homogenizer should be cleaned so that it is RNase-free. At a minimum will require
.3 ). Concatamers of tags are cloned and sequenced to yield a STAGE library. Tags in the library represent DNA fragments that were occupied by the DNA?binding protein, and mapping these tag sequences to the genome identifies the binding loci of the DNA?binding
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