| 产品详情 |
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| Product Name | Recombinant Human Myosin-9 (MYH9) , partial |
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| Description | 2-241aa, partial. MW: 159,864 Da. Purity >85% (SDS-PAGE). 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 macrothrombocyt |
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| Size | 0.05 mg (E-Coli), 0.2 mg (E-Coli), 0.05 mg (Baculovirus), 0.5 mg (E-Coli), 0.2 mg (Yeast) |
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| Concentration | n/a |
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| Applications | n/a |
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| Other Names | [myosin-9; Myosin-9; myosin-9; myosin heavy chain 9; Cellular myosin heavy chain, type A; Myosin heavy chain 9; Myosin heavy chain, non-muscle IIa; Non-muscle myosin heavy chain A; NMMHC-A; Non-muscle myosin heavy chain IIa; NMMHC II-a; NMMHC-IIA] |
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| Gene, Accession, CAS # | MYH9, Gene ID: 4627, Accession: NP_002464.1 |
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| Catalog # | MBS718871 |
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| Order / More Info | Recombinant Human Myosin-9 (MYH9) , partial from MYBIOSOURCE INC. |
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| Product Specific References | n/a |
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