Figure 1
Figure 1. Flow cytometric analysis of HEK293 cells expressing murine WT or R84A EPCR. (A) HEK293 cells were stably transfected with pcDNA3.1(−) vector only (left), or vectors containing the cDNA encoding murine WT (middle) or R84A (right) EPCR. EPCR expression was measured by incubating transfected HEK293 cells with FITC-IgG isotype control (filled histogram) or FITC-labeled goat polyclonal EPCR antibody (gray line). (B) Stably transfected HEK293 cells expressing WT or R84A mEPCR were incubated with murine Fl-APC (0-500 nM) in the presence of 3 mM CaCl2 and 0.6 mM MgCl2 for 15 minutes at room temperature and binding of Fl-labeled protein to cells expressing mEPCR was analyzed by flow cytometry. IgG, immunoglobulin G.

Flow cytometric analysis of HEK293 cells expressing murine WT or R84A EPCR. (A) HEK293 cells were stably transfected with pcDNA3.1(−) vector only (left), or vectors containing the cDNA encoding murine WT (middle) or R84A (right) EPCR. EPCR expression was measured by incubating transfected HEK293 cells with FITC-IgG isotype control (filled histogram) or FITC-labeled goat polyclonal EPCR antibody (gray line). (B) Stably transfected HEK293 cells expressing WT or R84A mEPCR were incubated with murine Fl-APC (0-500 nM) in the presence of 3 mM CaCl2 and 0.6 mM MgCl2 for 15 minutes at room temperature and binding of Fl-labeled protein to cells expressing mEPCR was analyzed by flow cytometry. IgG, immunoglobulin G.

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