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| Product Name | Recombinant Mouse Kalirin (Kalrn) , partial |
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| Description | MW: 116,985 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 the huntingtin-associated protein 1, which is a huntingtin binding protein that may function in vesicle trafficking. Alternatively spliced transcript variants encoding different isoforms have been described. |
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| Size | 0.05 mg (E-Coli), 0.05 mg (Yeast), 0.2 mg (E-Coli), 0.05 mg (Baculovirus), 0.5 mg (E-Coli) |
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| Concentration | n/a |
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| Applications | n/a |
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| Other Names | [kalirin isoform 2; Kalirin; kalirin; kalirin, RhoGEF kinase; Protein Duo; Serine/threonine-protein kinase with Dbl- and pleckstrin homology domain] |
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| Gene, Accession, CAS # | Kalrn, Gene ID: 545156, Accession: NP_001157740.1 |
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| Catalog # | MBS952190 |
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| Price | |
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| Order / More Info | Recombinant Mouse Kalirin (Kalrn) , partial from MYBIOSOURCE INC. |
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| Product Specific References | n/a |
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