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Description
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 nonsyndromic sensorineural deafness autosomal dominant type 17, Epstein syndrome, Alport syndrome with macrothrombocytopenia, Sebastian syndrome, Fechtner syndrome and macrothrombocytopenia with progressive sensorineural deafness. [provided by RefSeq
Specifications
Specifications
| Antigen | MYH9 |
| Applications | Immunofluorescence, Immunohistochemistry (PFA fixed) |
| Classification | Polyclonal |
| Conjugate | Unconjugated |
| Description | Rabbit polyclonal antibody raised against recombinant MYH9 |
| Dilution | Immunohistochemistry(1:1000-1:2500) Immunofluorescence(1-4 ug/ml) The optimal working dilution should be determined by the end user. |
| Formulation | In PBS, pH 7.2 (40% glycerol, 0.02% sodium azide) |
| Gene | MYH9 |
| Gene Alias | DFNA17/EPSTS/FTNS/MGC104539/MHA/NMHC-II-A/NMMHCA |
| Gene Symbols | MYH9 |
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