Paul.Cullen at med.monash.edu.au
Sun Sep 24 22:38:12 EST 2000
Are you pre-wetting the membrane with methanol before assembling the
transfer apparatus? I've found this to be necessary with Immobilon P.
> I have been having a lot of problems with efficiency of transfer from
> gel (10% acrylamide/bis) to PVDF membrane (Immobilon P). When I stain
> the gel after transfer, there is a lot of protein left on there. I know
> that I am not exceeding the binding capacity of the membrane (I did a
> titration of ug protein loaded and discovered that the ratio of protein
> transferred to those that stay behind is the same).
> The protein of interest is high moleculat weight (around 160
> kDa). I have tried :
> - reducing MeOH concetration in the buffer from 20% to 10 %.
> - doing an O/N transfer (25 V) followed by 1/2 hr 100 V
> - doing a 2 hr 100 V transfer
> Nothig really helps. Somethimes there is enough protein for me to see (I
> use LumiLight, Roche) and sometimes there's not. So help, please !! Are
> high mol wt proteins transferred better at high or low field strength ?
> Has anyone tried SDS in the transfer buffer ?
Bacterial Pathogenesis Research Group
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