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全部话题 - 话题: primerbank
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A******y
发帖数: 2041
1
来自主题: Biology版 - how to design primers for qPCR?
Just use primerbank, it is really 80-90% to give you a usable RT-primer.
Here we go: http://pga.mgh.harvard.edu/primerbank/
m*****n
发帖数: 760
2
来自主题: Biology版 - 最近PrimerBank能用吗?
想设计一些RT-PCR引物,怎么老是server error?
a****d
发帖数: 1919
3
来自主题: Biology版 - 最近PrimerBank能用吗?
got same problem
I used other online tools instead, like IDT
s******r
发帖数: 1245
4
去harvard的primerbank里找你的基因,老鼠的很多都有,一个基因会有不止一对,有
的还有validation data,自己试一下挑最好用的
A******y
发帖数: 2041
l***s
发帖数: 841
6
这浓度也太高了吧。为什么不用标准protocol?要降低10倍。还有primer dimer 的话
,重新设计引物。从这里找:
http://pga.mgh.harvard.edu/primerbank/
l**********1
发帖数: 5204
7
来自主题: Biology版 - 请教Southern blot问题
模板通过PCR获得 then TA sub cloning, then pick up clone do sequencing for
check the probe sequencing or not?
if not how to prove that PCR product as Dig probe without any mutation
if all above steps were done
then might need to PCR about 1kp product as probe
please refer
Primer design
http://pga.mgh.harvard.edu/primerbank/
original hint was from
http://www.mitbbs.com/article_t/Biology/31807477.html
19th floor post
A******y
发帖数: 2041
8
How about go find a new primer using the data base?
http://pga.mgh.harvard.edu/primerbank/
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