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Blue native PAGE problems

Blue native PAGE problems - Protein Forum

Blue native PAGE problems - Protein Forum

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Old 06-21-2007, 07:33 AM
Hubert Mayerhofer
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Default Blue native PAGE problems


I'm trying to carry out a blue native PAGE as described in the paper by
Ilka Wittig, Hans-Peter Braun and Hermann Schägger in Nature Protocols
1, - 418 - 428 (2006).

Yet if I don't load any protein just to test everything the running
front looks nice. When I load my protein I don't get a sharp band
normally I get smearing over the whole separation gel. I could reduce
this by diluting the protein and now I'm getting something like a zigzag

I prepared the buffers accordingly to the protocol in the paper yet I
didn't cast a gradient gel but a homogenous one as this was also
described to work in a different paper (Reif, S., Voos, W. & Rassow, J.
Intramitochondrial dimerization of citrate synthase characterized by
blue native electrophoresis. Anal. Biochem. 288, 97–99 (2001).) (and to
simplify the casting as I'm lacking the equipment).

Yet I got the impression that this type of gel is normally used for
membrane proteins while I try to use it with soluble proteins. Could
this be the reason that the coomassie doesn't find the required amount
of hydropobic patches on the protein preventing the formation of a sharp

Are there any changes required for soluble proteins or does anyone have
some other suggestions?

thanks in advance

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Old 06-25-2007, 08:24 PM
Dr Engelbert Buxbaum
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Default Blue native PAGE problems

Am 21.06.2007, 03:33 Uhr, schrieb Hubert Mayerhofer <[Only registered users see links. ]>:

You could cast a step gradient (10--12 steps) to test this, as such gel
give essentially the same result as linear gradients. This requires not
much equipment except a steady hand ;-)
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Old 06-11-2010, 11:22 AM
Pipette Filler
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Default Blue native PAGE problems

I Have big problems with blue native, I used a Invitrogen Blue native kit, and detect my proteins with immunoblotting, but in my results I get smearing over part of gel, only one, my proteins are obtein mediated transfection, I used digitonin 1% to solubilize membranes of cellular extract, What Can I do, to obtain band of my proteins???
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