I would appreciated any suggestions to facilitate sorting CHO cells which express VE-cadherin. These cells tend to aggregate making sorting difficult. Vortexing seems to increase aggregation. These adherent cells are removed from the culture flask using trypsin("Cell Stripper"). I try to keep the cell concentration low which helps somewhat, but is not ideal. Is any buffer available that will not destroy VE-cadherin? Thanks in advance, Paul L. Hallberg Flow Cytometry Manager KCC CORE Flow Cytometry Facility Thomas Jefferson University 215-503-4556 215-923-0249(fax) Paul.Hallberg@mail.tju.edu
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