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作 者:黄惠民[1] 陈莹[1] 邱丽君[1] 史桂英[1]
机构地区:[1]上海第二医科大学附属新华医院,上海第二医科大学生物物理教研室
出 处:《中华血液学杂志》1995年第9期471-472,共2页Chinese Journal of Hematology
基 金:国家自然科学基金
摘 要:在洗涤血小板悬液中加入不同浓度纤维蛋白溶酶(纤溶酶)后,FACS测得的抗GPIb单克隆抗体(单抗)的荧光结合强度随纤溶酶浓度的增加而逐渐下降,中止纤溶酶作用并无明显恢复。正常血小板经TritonX~100处理后,抗GPIb单抗荧光结合强度明显增加。纤溶酶作用后的洗涤血小板无论是否经TritonX-100处理,抗GPIb单抗荧光结合强度均明显减弱,但处理者为甚。ffect of plasmin on platelets glycoprotein Ib(GPIb)was studied with flow cytometer. The fluorescencebinding density of anti-GPIb monoclonal antibody(mAb) was reduced gradually with the plasmin con-centration increasing and there was no density restora-tion after plasmin effects were terminated and plateletswere incubated for one to three hours at 22℃. Thedensity of anti-GPIb mAb increased significantly whenplatelets were pretreated with Triton-100. After plas-min treatment , the density in both samples , Pretreatedor not with Triton-100, was reduced significantly
分 类 号:R331.143[医药卫生—人体生理学]
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