I am interested in hearing about peoples experience (good or bad) with this technology. I am considering using these gels to normalize for gel loading on immunoblots. Please share your input. Thanks
I used to cast my own gels, then Bio-Rad sent a selection of gels free with an order and I never went back to casting my own gels. This was partly due to me being lazy and also due to the usefulness of the stain-free normalisation.
To blot I used PVDF membrane and a semi-dry blotting protocol.
One thing I did notice proteins under 25 kDa did not work as well as larger proteins this could be attributed to the blotting protocol we used rather than separation during electrophoresis.