In article <siyer-0510961811450001 at bmg146.cmc.uab.edu>,
siyer at bmg.bhs.uab.edu (Arioch) wrote:
> anybody know of a good protocol to remove the salt from samples
>before they are loaded on to SDS-PAGEs?? i have found out that hi salt
>tends to distort the way the bands run on the gel (screwing up the
>electrical field and therefore affecting protein mobility). i found this
>one protocol that tells you to add 0.15% deoxycholic acid, incubate for 10
>min followed by addition of TCA ---> spin for about 15 min at 3000g --->
>decant all the TCA and resuspend pellet (containing precipitated protein
>with presumably no salt). this however has not been too successful (for
>me) and still causes distortion of my gel bands (much annoyance). anybody
>know of any modicfications to this protocol or other protocols that
>work?? thanks much...
>You might try microfiltration or dialysis on a micro scale.