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Questions related from Georgiana Toma
Sometimes when I sort CD8+ cells first from PBMCs and then CD4+ cells, I get a very good purity with the CD8+ beads and a lousy purity with the CD4 beads. I try to keep the beads, buffer, even the...
05 October 2018 9,724 1 View
I am supposed to look at a certain protein by FACS in naive and memory T cells from PBMCs of healthy blood donors. The naive-memory panel i used is: CD3, CD4, CD8, CD45RA and CCR7 At 0h when the...
27 April 2018 9,781 2 View