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重组肌球蛋白重链9
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。

重组肌球蛋白重链9(MYH9)
Recombinant MYH9
基因名:

MYH9


产品别名:

BDPLT6; DFNA17; EPSTS; FTNS; MATINS; MHA; NMHC-II-A; NMMHC-IIA; NMMHCA; MYH9; myosin heavy chain 9; myosin heavy chain 9; myosin-9; cellular myosin heavy chain, type A; myosin, heavy chain 9, non-muscle; non-muscle myosin heavy chain 9; non-muscle myosin heavy chain A; non-muscle myosin heavy chain IIa; non-muscle myosin heavy polypeptide 9; nonmuscle myosin heavy chain II-A; 肌球蛋白重链9; 肌球蛋白重链9(MYH9);


背景信息:
Cellular myosin that appears to play a role in cytokinesis, cell shape, and specialized functions such as secretion and capping. Defects in MYH9 are the cause of May-Hegglin anomaly (MHA) . MHA is an autosomal dominant macrothrombocytopenia characterized by thrombocytopenia, giant platelets and leukokyte inclusions appearing as highly parallel paracrystalline bodies.
 
 
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