I think different pH is maintained to obtain greater resolution.In the
stacking gel the sample protein moves faster as compared to resolving gel.
and  while reaching the seperating gel the protein moves gently and a
greater resolution is obtained.

On 11/13/08, puneet sharma <[EMAIL PROTECTED]> wrote:
>
> dear
>  the ph of the separating gel and stacking gel is different.
> i think the ph of the stacking gel is 4.2 and separating gel is 6.2 on the
> basais of this difference the different pattern of bands are appeared on the
> gel.ph can be measured with ph meter or litmus paper.
>
>
>  On Sat, Nov 8, 2008 at 1:51 PM, 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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