Fig. 1.
Fig. 1. Immunoblot analyses of GPIIIa (nonreduced) and GPIIb (reduced). SDS-solubilized platelets (1 μL of 5 × 107platelets/mL) were electrophoresed into a 7.5% polyacrylamide gel, electrotransferred onto PVDF membranes, and developed as previously described.31 (A) Control, patient, and two other GT patient samples with mutations in GPIIIa (I-J: Iraqi-Jewish) and GPIIb (Arab)44 were run under nonreduced conditions. The membranes were incubated with the anti-GPIIIa specific murine MoAb, 7H2.29 The arrow indicates the position of GPIIIa. (B) Two patient samples prepared on different dates (January 1990 and February 1995) and a control sample were run under reduced conditions. The membranes were incubated with the anti-GPIIb heavy chain specific murine MoAb, PMI-1.3233 The solid arrow indicates the position of proGPIIb, the open arrow, mature processed GPIIb, and the arrow head an abnormally migrating fragment.

Immunoblot analyses of GPIIIa (nonreduced) and GPIIb (reduced). SDS-solubilized platelets (1 μL of 5 × 107platelets/mL) were electrophoresed into a 7.5% polyacrylamide gel, electrotransferred onto PVDF membranes, and developed as previously described.31 (A) Control, patient, and two other GT patient samples with mutations in GPIIIa (I-J: Iraqi-Jewish) and GPIIb (Arab)44 were run under nonreduced conditions. The membranes were incubated with the anti-GPIIIa specific murine MoAb, 7H2.29 The arrow indicates the position of GPIIIa. (B) Two patient samples prepared on different dates (January 1990 and February 1995) and a control sample were run under reduced conditions. The membranes were incubated with the anti-GPIIb heavy chain specific murine MoAb, PMI-1.32,33 The solid arrow indicates the position of proGPIIb, the open arrow, mature processed GPIIb, and the arrow head an abnormally migrating fragment.

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