Fig. 4.
Fig. 4. Homocysteine increases the stable association between GRP78 and vWF. HUVEC cultured in the absence or presence of 0.2, 1.0, or 5.0 mmol/L homocysteine for 8 or 18 hours were metabolically labeled for 1 hour in the presence of [35S]methionine and [35S]cysteine. Radiolabeled proteins from cell lysates were immunoprecipitated with anti-vWF antibodies, separated on 7.5% SDS polyacrylamide gel under reducing conditions, and detected by fluorography. Immunoprecipitation of pro and mature vWF coprecipitated GRP78. kD, molecular mass markers.

Homocysteine increases the stable association between GRP78 and vWF. HUVEC cultured in the absence or presence of 0.2, 1.0, or 5.0 mmol/L homocysteine for 8 or 18 hours were metabolically labeled for 1 hour in the presence of [35S]methionine and [35S]cysteine. Radiolabeled proteins from cell lysates were immunoprecipitated with anti-vWF antibodies, separated on 7.5% SDS polyacrylamide gel under reducing conditions, and detected by fluorography. Immunoprecipitation of pro and mature vWF coprecipitated GRP78. kD, molecular mass markers.

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