Cloning large inserts into pGEM7F

[John R. McQuiston]

It depends on how big they are, whether the gene(s) are toxic to E.coli.....
If they're big they could be shearing.  Give me (us) more info either on the 
newsgroup or directly and I'll see if I can help.

I have cloned a 30kb fragment into pGEM 3z but I used a kan gene tagged on it 
to select and maintain it.  



John R. McQuiston

Foodborne Diseases Branch
Centers for Disease Control and Prevention
Atlanta Ga

In article <7344ti$168m at majestix.uni-muenster.de>, jackisc at uni-muenster.de 
says...
>
>Hi!
>
>Since 4 weeks now, we are trying to clone two XhoI/XhoI-cut fragments into the 
>pGEM7F vector. Has anyone any experience and helpful hints for cloning such 
>fragments in this or any other system?? 
>
>Thanks, Bjoern
>
>bo.jackisch at uni-muenster.de
>