血管性血友病
血管性血友病因子
医学
免疫学
计算生物学
生物
血小板
作者
Susan Oliver,Kun Kan Edwin Lau,Kent Chapman,Emmanuel J. Favaloro
出处
期刊:Methods in molecular biology
日期:2017-01-01
卷期号:: 495-511
被引量:35
标识
DOI:10.1007/978-1-4939-7196-1_36
摘要
Von Willebrand disease (VWD) is reportedly the most common inherited bleeding disorder and can also arise as an acquired syndrome (AVWS). These disorders develop due to defects and/or deficiency of the plasma protein von Willebrand factor (VWF). Laboratory testing for the VWF-related disorders requires assessment of both VWF level and VWF activity, the latter requiring multiple assays because of the many functions carried out by VWF to help prevent bleeding. As an additional step, an evaluation of VWF structural features by multimer analysis is useful in selective investigations. The current paper therefore describes a protocol for assessment of VWF multimers by gel electrophoresis, thus enabling identification of protein bands that represent differently sized multimers. The sample protocol described in this chapter is the methodology developed by Sebia.
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