Fig. 4.
Fig. 4. Effects of GRGDS peptide plus EGTA on p72syk-associated tyrosine kinase activity induced by botrocetin-vWF. Platelets were incubated with or without 200 μmol/L GRGDS peptide plus 1 mmol/L EGTA (instead of Ca2+) for 5 minutes and then activated with 3 μg/mL of botrocetin and 10 μg/mL of vWF for the indicated time intervals. For analysis of p72syk autophosphorylation, reactions were terminated by adding lysis buffer. p72syk was immunoprecipitated with anti-p72syk MoAb, and the sample was Western-blotted using antiphosphotyrosine MoAb, 4G10. The arrowhead represents the band presumably derived from IgG heavy chains. The data are representative of three experiments.

Effects of GRGDS peptide plus EGTA on p72syk-associated tyrosine kinase activity induced by botrocetin-vWF. Platelets were incubated with or without 200 μmol/L GRGDS peptide plus 1 mmol/L EGTA (instead of Ca2+) for 5 minutes and then activated with 3 μg/mL of botrocetin and 10 μg/mL of vWF for the indicated time intervals. For analysis of p72syk autophosphorylation, reactions were terminated by adding lysis buffer. p72syk was immunoprecipitated with anti-p72syk MoAb, and the sample was Western-blotted using antiphosphotyrosine MoAb, 4G10. The arrowhead represents the band presumably derived from IgG heavy chains. The data are representative of three experiments.

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