Virash Gupta wrote: >
Seperating 3.5 and 3.3 kb in agarosegel. [How to do it...]
>
Purify DNA and clone in a PCR cloning vector and slect clones for right insert.
Given that you will need to clone the DNA and select clones no matter what, it may be simpler just to clone the starting mixture, depending on the relative intensity of your two bands.
Peter _______________________________________________ Methods mailing list [email protected] http://www.bio.net/biomail/listinfo/methods
