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Questions related from Fabian Recker
Good evening, I am wondering why sometimes I only have very few cells on my cover slip, after staining. Could it have something to do with my washing procedure? I allways wash 3x with 1ml pbs in...
01 July 2022 5,412 3 View
Good evening, so my question is about chemilumiscence. So when I use a rabbit primary antibody for.my phosphorylated protein, put the rb-HRP 2. antibody on it and envelope it with ECL-solution,...
17 May 2022 7,463 1 View
Good Evening, I have a question about the normalisation of my results when measuring phoshorylated proteins. Example: EGF stimulation experiment: I measure phoshorylation of AKT as a function...
31 December 2021 3,875 1 View
Good Afternoon, the Blot was blocked in 3%BSA/TBST for 1hour, then treated with Akt1/2/3 (SantaCruz, 1:500 in 3%BSA/TBST), ms HRP and ECL, and then developed in Fusion FX. Due to the high...
30 November 2021 3,322 3 View
Maybe you have some ideas about where this backround is coming from? I am not sure if this comes from blotting, blocking or if this is dirt? Thank you very much in advance!
09 November 2021 8,629 3 View