G50 remove hot oligos?

[Raj Shankarappa]

Jim:
				I am not sure whether G50 spin would be ideal with regard to both 
the resolution and yield.  To separate unligated adapters, I have had 
good results with a simple PEG precipitation.  The yield has been good 
and the procedure is quite simple.  Standard PEG ppt protocols should 
work fine.  Let me know if you need a detailed protocol.

Raj Shankarappa
rajs at u.washington.edu
  

jgraham at bronze.ucs.indiana.edu (the End) wrote:
>Hello,
>
>Has anyone tried to send radiolabled oligos through a G50 spin
>column to see if they are effectively retained? Perhaps a 
>a CL-4(6)B? I need to separate double stranded linkers
>from a cDNA insert with as few steps as possible (no gel).
>
>Thanks much, E-mail copies please,
>
>Jim
>J. Graham PhD 
>Biology Department 
>Washington University of St. Louis 
>
>