Can any one provide me appropriate protocol for preparing crude mouse tissue lysate for western blotting. The protein of interest resides both in cytoplasm and nucleus so which lysis buffer would be appropriate?
I agree with Mirsada, RIPA buffer solubilizes all membranes. However, RIPA buffer breaks interactions between proteins, so it also depends what the purpose of your experiment is.
If you don't need nuclear proteins and if you want to preserve protein-protein interactions and protein structure integrity I would recommend either NP40 or TritonX buffer. CHAPS buffer is a bit stronger than NP40 and TritonX, but preserves some protein interactions.
I resuspend the tissue in the buffer, keep the sample on ice for 30' and resuspend every 10'. You can also use a homogenizer/sonicator. Spin down @ 13200rpm, and collect the supernatant.
I saw that you made approx. 20% homogenate from rat tissue for western blot as you have mentioned in the protocol (used ~5ml RIPA for 1g of tissue). Do you have reference in support of it? It will be very helpful if you provide it here.
Dear Shubhashish I am working on my MSc project. I am wondering about the final protocol you used for your research. I need to know the exact protocol of extraction protein from the rat brain for WB. I will be appreciated. sincerely solmaz