由买买提看人间百态

boards

本页内容为未名空间相应帖子的节选和存档,一周内的贴子最多显示50字,超过一周显示500字 访问原贴
Biology版 - DNA T7 测序结果 NO band, NO data
相关主题
请推荐好的DNaseHow to study DNA hairpin? Nuclease S1?
EMSA 的问题柱层材料国内到现在用于生物的一些产品咋还是做不好呢?
ChIP-qPCR primer设计next generation sequencing
paper help please, fabaozi thanks!奇怪的PCR结果
TA克隆的问题,从飞机失联开始到现在都没搞定digest 100ug plasmid DNA 最小体积多少啊?
请教:突变基因,如何进行 primer sequence design?关于Luciferase Asssay
Re: 请教求教dual luciferase reporter assay经验指点
mammalian cells transfection 后 integration 的效率大概是多少?问个sequencing的初级问题
相关话题的讨论汇总
话题: t7话题: cat话题: promoter话题: primer话题: dna
进入Biology版参与讨论
1 (共1页)
M*******C
发帖数: 183
1
同一个DNA样品,根据vector map,T3, T7 两个方向测序,primer都是测序中心提供。
T3的结果正常,T7却NO band, NO data。 再测一次,还是这样。
大家觉得这是怎么回事?thx
b***8
发帖数: 31
2
From Promega:
Due to a sequence
difference between the T7 Promoter Primer (Cat.# Q5021) and the T7 RNA
polymerase promoter in the pCI-neo Mammalian Expression Vector, the T7
Promoter Primer cannot be used for sequencing these expression vectors. The
sequence difference is downstream of the transcriptional start site and is
located at the 3′-end of the T7 Promoter Primer. The T7 EEV (Eukaryotic
Expression Vector) Promoter Primer (Cat.# Q6700) has been designed
specifically to prime sequencing reactions from the mammalian expression
vectors, pCI-neo (Cat.# E1841), pSI (Cat.# E1721), pCI (Cat.# E1731) and
pALTER®-MAX (Cat.# Q5761).
M*******C
发帖数: 183
3
原来如此!
多谢

The

【在 b***8 的大作中提到】
: From Promega:
: Due to a sequence
: difference between the T7 Promoter Primer (Cat.# Q5021) and the T7 RNA
: polymerase promoter in the pCI-neo Mammalian Expression Vector, the T7
: Promoter Primer cannot be used for sequencing these expression vectors. The
: sequence difference is downstream of the transcriptional start site and is
: located at the 3′-end of the T7 Promoter Primer. The T7 EEV (Eukaryotic
: Expression Vector) Promoter Primer (Cat.# Q6700) has been designed
: specifically to prime sequencing reactions from the mammalian expression
: vectors, pCI-neo (Cat.# E1841), pSI (Cat.# E1721), pCI (Cat.# E1731) and

1 (共1页)
进入Biology版参与讨论
相关主题
问个sequencing的初级问题TA克隆的问题,从飞机失联开始到现在都没搞定
请教DNA长度的一个问题请教:突变基因,如何进行 primer sequence design?
mammalian cell genomic DNA extractionRe: 请教
每个细胞都有一样的DNA?mammalian cells transfection 后 integration 的效率大概是多少?
请推荐好的DNaseHow to study DNA hairpin? Nuclease S1?
EMSA 的问题柱层材料国内到现在用于生物的一些产品咋还是做不好呢?
ChIP-qPCR primer设计next generation sequencing
paper help please, fabaozi thanks!奇怪的PCR结果
相关话题的讨论汇总
话题: t7话题: cat话题: promoter话题: primer话题: dna