| 产品详情 |
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| Product Name | Recombinant Rat Huntingtin-associated protein 1 (Hap1) |
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| Description | 1-629aa, Full length protein. MW: 67,004 Da. Purity >85% (SDS-PAGE). Huntington s disease (HD), a neurodegenerative disorder characterized by loss of striatal neurons, is caused by an expansion of a polyglutamine tract in the HD protein huntingtin. This gene encodes a protein that interacts with huntingtin, with two cytoskeletal proteins (dynactin and pericentriolar autoantigen protein 1), and with a hepatocyte growth factor-regulated tyrosine kinase substrate. The interactions with cytoskeletal |
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| Size | 0.05 mg (E-Coli), 0.05 mg (Baculovirus), 0.2 mg (E-Coli), 0.05 mg (Mammalian-Cell), 0.2 mg (Yeast) |
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| Concentration | n/a |
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| Applications | n/a |
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| Other Names | [huntingtin-associated protein 1 isoform A; Huntingtin-associated protein 1; huntingtin-associated protein 1; huntingtin-associated protein 1] |
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| Gene, Accession, CAS # | Hap1, Gene ID: 29430, Accession: NP_077047.1 |
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| Catalog # | MBS718762 |
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| Order / More Info | Recombinant Rat Huntingtin-associated protein 1 (Hap1) from MYBIOSOURCE INC. |
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| Product Specific References | n/a |
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