Hi,
I want to sort fibroblast from a mice, than fix them and stain it for immunofluorescence. I dont want to culture it first.
I have no experience with that. What is the best way to do it?
Hello
look at links here will help you
Good Luck
http://medicine.yale.edu/labmed/cellsorter/protocols/staining.aspx
http://www.ebioscience.com/resources/best-protocols/flow-cytometry-protocols.htm
http://flowcytometry.uchc.edu/pdfs/protocols/cellstaining.pdf
http://services.medicine.uab.edu/PublicDocuments/ImmRheum/FACS%20sorting%20protocol.pdf
You need to establish a good validation protocol that includes a viability stain in your stained tubes. Washing buffer is important, I suggest to use colorless RPMI media. I also suggest to validate fixation before and after staining.
Hi, So have you done this? I'm going to stain my samples after sort so I wonder if you found a method to do so.
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