hey..

In SDS-PAGE, stacking gel has larger pore size than the resolving
gel,,,,,, if u have done SDS-PAGE, u must have maintained different
voltage-current when the sample proteins runs through the stacking gel
(~70 V) and resolving gel (~ 150 V) ..... it must be due to the same
resason different pH should be maintained


On Nov 8, 11:51 am, "Vijayashree Navali"
<[EMAIL PROTECTED]> wrote:
> hello frnds,
>
>                 can anybody explain me y we hv 2 maintain different pH for
> separating gel & stacking gel in SDS PAGE???????????

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