d*i
2 楼
google了半天拿不定主意。。有商用的最好。
a*e
4 楼
SV40 NLS: PKKKRKV
l*l
5 楼
求細節。
d*i
6 楼
我是想把目的蛋白和核定位信号序列融合构成plasmid,希望转染后表达的蛋白都进到
细胞核内。这种融合的时候在NLS和目的基因之间要加其他序列吗?不会就这么硬生生
的连在一起吧?谢谢!
细胞核内。这种融合的时候在NLS和目的基因之间要加其他序列吗?不会就这么硬生生
的连在一起吧?谢谢!
b*y
7 楼
Check Yuh Min Chook's studies. There are many options. Of course, the one
suggested by ahche works. As far as linkers are concerned, a GGS linker in
between should do it. If your protein is intrinsically disordered at the
location of linkage, direct fusion should also do it. What matters is the
availability of the NLS to importin(s).
suggested by ahche works. As far as linkers are concerned, a GGS linker in
between should do it. If your protein is intrinsically disordered at the
location of linkage, direct fusion should also do it. What matters is the
availability of the NLS to importin(s).
相关阅读
concentration and kinds of detergent for cell (293T) lysis?说点实际问题,到底博后工资多少啊?回国工作国内大学提供的条件 (转载)这篇谈职业生涯的文章?怎么找RNA splicing variants? 有相关的数据库吗?生物版最有文化求助:欧洲开会,回美签证问题生物PhD想进工业界,不知有什么职位适合包子,求一篇文章问个问题问个cloning 的问题古代的表亲婚姻 (转载)Funding: Australia's grant system wastes timeWhat does X^X and X^Y mean for drosophila genetics?打听一个PI:Yi Zheng @ Cincinnati, Ohio有人恢复过超级计算机上的删除的目录吗?如果你有100万RMB科研启动资金建自己的新lab哪里可以找到time-series Alzheimer‘s disease gene expression data?2013 Gairdner Award生物千老的家事