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问个分子克隆的问题,求助大拿...
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问个分子克隆的问题,求助大拿...# Biology - 生物学
a*n
1
感觉怎么样?
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s*r
2
在做一个targeting vector,总长17kb多。现在做到最后一步克隆了,把一个4.4kb的
片段用BamHI切下来,装到BclI线性化的12kb backbone里。已经反复做了几次,每次8-
12miniprep里面90%都是一个大小3kb的奇怪质粒,偶尔出来的几个大小正确的测序发现
全部都是反向。先前怀疑是由于质粒太大在E.coli里发生重组,这次换成了stbl3的感
受态,还是一样的结果。求有经验的给点建议...
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w*d
3
I encountered a similar problem previously.
Someone told me that writhing of a circular DNA may occur when the insertion
is too long. If this cannot be tolerated during replication, the circular
DNA will not be amplified.
Finally, I changed another vector to fix it.
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m*5
4
by which method did you dephorsphorylate your plasmid? I usually got most of
plasmid self ligased
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c*g
5
CIP from NEB is pretty good.

of

【在 m******5 的大作中提到】
: by which method did you dephorsphorylate your plasmid? I usually got most of
: plasmid self ligased

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s*r
6
Yes, I CIPed the vector for 1h, but it didnt appears to be self ligation.
The 3kb plasmid is weird, because the vector itself is 12kb.
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a*p
7
17k还用酶切,还是单酶切? 真牛呀。 用重组吧
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m*5
8
??? detail??

【在 a******p 的大作中提到】
: 17k还用酶切,还是单酶切? 真牛呀。 用重组吧
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a*p
9
A highly efficient recombineering-based method for generating conditional
knockout mutations
看看这片文章,然后朝作者要个能重组的菌
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I*a
10
让E。coli长慢一点,
以前遇到这种情况,
我每次都筛选几十个或是上百个克隆,有时候会有对的,
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