Fig. 1.
Fig. 1. Characterization of hP2X7 receptor MoAb by flow cytometry with HEK293 cells stably transformed with (A) hP2X1, (B) hP2X4, or (C) hP2X7. Cells detached with PBS plus 1 mmol/L EDTA were incubated on ice with 15 μg/mL purified antibody for 30 minutes. The MoAb (bold line) was detected with an FITC-labeled sheep antimouse F(ab′)2fragment. An IgG2b antibody (thin line) was used as an isotype control.

Characterization of hP2X7 receptor MoAb by flow cytometry with HEK293 cells stably transformed with (A) hP2X1, (B) hP2X4, or (C) hP2X7. Cells detached with PBS plus 1 mmol/L EDTA were incubated on ice with 15 μg/mL purified antibody for 30 minutes. The MoAb (bold line) was detected with an FITC-labeled sheep antimouse F(ab′)2fragment. An IgG2b antibody (thin line) was used as an isotype control.

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