Hi,
I am looking to try a cross-linking protocol to assess alpha-synuclein species in my adherent cells. I have DSS for this and have found several papers with a semi-descriptive method but I have several questions. Primarily, what is a suitable volume of the DSS solution to add to these cells? I have cells in a 6cm plate with approx. 500,000 cells. I have also seen some protocols where this method is done when cells are lysed first and the reactions take place in a tube, so I am not sure if one is more effective than the other. If anybody has any tips for using DSS with adherent cells, I would be very grateful!
Thanks in advance