Myosin-9 (MYH9) Antibody
This gene encodes a myosin IIA heavy chain that contains an IQ domain and a myosin head-like domain. The protein is involved in several important functions, including cytokinesis, cell motility and maintenance of cell shape. Defects in MYH9 are the cause of non-syndromic sensorineural deafness autosomal dominant type 17, Epstein syndrome, Alport syndrome with macrothrombocytopenia, Sebastian syndrome, Fechtner syndrome and macrothrombocytopenia with progressive sensorineural deafness.
Supplier | Abbexa Ltd. |
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Product # | abx030030-80UL |
Pricing | 80 µl USD $326.25 |
Clonality | Polyclonal |
Conjugation | Unconjugated |
Host | Rabbit |
Tested Applications | ELISA, WB |
UniProt Primary AC | P35579 |
Dry Ice | No |
Availability | Shipped within 5-10 working days. |
Note | This product is for research use only. |