About 50 and 55 kDa.
Ranen

On Thu, Nov 11, 2010 at 7:04 PM, <[email protected]>wrote:

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>   1. Separation by Superose 6 gel filtration (ranen aviner)
>   2. Re: Separation by Superose 6 gel filtration (WS)
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> Message: 1
> Date: Thu, 11 Nov 2010 11:14:22 +0200
> From: ranen aviner <[email protected]>
> Subject: Separation by Superose 6 gel filtration
> To: [email protected]
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> Dear all,
>
> I'm running cell lysate on superose 6 followed by SDS-PAGE WB. While my
> protein of interest is detected as a single band in the unfractionated
> lysate (i.e. total protein), it reproducibly migrates as two discrete bands
> in superose 6 fractions.
>
> Now, this is not a matter of relative concentration, because the two bands
> occur in ALL superose 6 fractions and cannot be detected in unfractionated
> lysate, even at up to 200ug total protein!
>
> My lysis buffer contains protease and phosphatase inhibitors, so this
> shouldn't be the problem.
>
> Any ideas as to why gel filtration chould affect the migration pattern of
> an
> individual protein?
>
> Thanks,
> Ranen Aviner
>
>
> ------------------------------
>
> Message: 2
> Date: Thu, 11 Nov 2010 07:15:13 -0800 (PST)
> From: WS <[email protected]>
> Subject: Re: Separation by Superose 6 gel filtration
> To: [email protected]
> Message-ID:
>        <[email protected]>
> Content-Type: text/plain; charset=ISO-8859-1
>
> What about the size of the bands you get?
>
> Wo
>
>
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> End of Methods Digest, Vol 66, Issue 6
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