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#1
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| I'm trying to detect a 7kDa protein by Western Blot. I've ran the cell lysate in a 15% acrylamide gel and the problem is, proteins bellow 14kDa just vanish. The Molecular standard is broad range (6-150kDa) and even the weight doesn't show in coomassie or in the ponceau (I've stained half the gel and transfered the other half). Does anyone has a tip or similar problem? Thanks |
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#2
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| In article <[Only registered users see links. ].net> , "Daniel Kerr" <[Only registered users see links. ]> wrote: Bis-Tricine gels have been developed precisely to combat a problem of poor resolution of small proteins/peptides. If your problem is actually a poor retention on membrane (make sure it is not a poor transfer first!), switching to a lower porosity (0.2 um) and higher capacity (PVDF) membranes combined with the removal of SDS from gel (15-30 min soak in transfer buffer before assembling the sandwich) should help. May also try increasing MeOH in transfer buffer to 30%. DK |
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#3
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| DK wrote: And of course: leave out the SDS from the transfer buffer. SDS increases mobilisation of large proteins, but reduces binding to the membrane. MeOH increases binding of small proteins to the membrane, but reduces mobility. Thus only one or the other are to be used, not both at the same time, as commonly seen. |
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| 7kda , electrophoresis , protein |
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