Abbreviation: MYH9
Target Synonym: MYH9;BDPLT6;DFNA17;EPSTS;FTNS;MHA;NMHC-II-A;NMMHC-IIA;NMMHCA;myosin-9
Conjugation: Unconjugated
UNIProt ID: P35579
Background: This gene encodes a conventional non-muscle myosin; this protein should not be confused with the unconventional myosin-9a or 9b (MYO9A or MYO9B). The encoded protein is a myosin IIA heavy chain that contains an IQ domain and a myosin head-like domain which is involved in several important functions, including cytokinesis, cell motility and maintenance of cell shape. Defects in this gene have been associated with non-syndromic sensorineural deafness autosomal dominant type 17, Epstein syndrome, Alport syndrome with macrothrombocytopenia, Sebastian syndrome, Fechtner syndrome and macrothrombocytopenia with progressive sensorineural deafness.
Concentration: 1mg/mL
Immunogen: Recombinant fusion protein of human MYH9
Dilution: WB 1:500-1:2000,IHC 1:50-1:200
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