Hello everyone,
I would like to take a advice from you all. I have protein like 200 KDa
when i lode in a gel it shows band on 200KDa, Is that this protein gets
dimer or anything else is happening.
I would appreciate for some open discussion.
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* Regards,** Arun *
can any one help me in suggesting that what mistake i have did in my mutagenic
pcr . actually my problem is my primer annealing temperature is 81degree. im
using phusion pol enzyme. i have made many trial, i.e., made annealing at 68
and then followed 2 step pcr method and then added 1micro lit