05 May 2015 2 607 Report

Hello Guys,

I have some questions regarding to buffer and method for cultured cell fractionation as following:

  • Can I just use PBS with some inhibitors for buffer? because what matter is centrifuge speed to dissociate cell organelles.
  • Can I use just mild lysis buffer (NP40 or tritonx100) to homoginize cell lysate instead of douce homoginizer before centrifuge each pellet?
  • Can I use sonication to homoginize cell lysate? Will it break nucleus of mitochondria before centrifuge?
  • There are so many recipe for the buffer and method for cell fractanation, which is the best or most standard protocol I should follow? Any paper suggestion?
  • Thank you so much

    More Asa Wu's questions See All
    Similar questions and discussions