I am having difficulty in finding out whether or not I should activate my cells or cell supernatant in order to measure the expression of Amphiregulin using a quantitative ELISA kit.
Has anybody any experience with this, or could advise me?
Thank you for the advice regarding the ADAM17 activation, however I wanted to ask another question.
If you have experience with this, what sort of control would you use to compare against the activated cells.
Surely the non-activated cells aren't a comparable control as one should not be able to measure the AREG shedding in the supernatant, when not activated?
Apologies if this is a very simple question, I'm not so well experienced with this type of work as of yet.