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| Product Name | IMPAD1, 34-359aa, Human, His tag, E Coli (Denatured) |
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| Description | MW: 37.6kDa (349aa). Purity >90% by SDS-PAGE. Inositol monophosphatase 3, also known as IMPAD1, is a member of the inositol monophosphatase family. IMPAD1 is localized to the Golgi apparatus and catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP). Mutations in this gene are a cause of GRAPP type chondrodysplasia with joint dislocations, and a pseudogene of this gene is located on the long arm of chromosome 1. Recombinant human IMPAD1 protein, fused to Hi |
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| Size | 0.1 mg, 0.5 mg |
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| Concentration | 1 mg/ml (determined by Bradford assay) |
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| Applications | SDS-PAGE |
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| Other Names | [Inositol monophosphatase 3; GPAPP; IMP 3; IMP-3; IMPA3] |
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| Gene, Accession, CAS # | IMPAD1, Gene ID: 54928, Accession: NP_060283 |
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| Catalog # | MBS205390 |
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| Order / More Info | IMPAD1, 34-359aa, Human, His tag, E Coli (Denatured) from MYBIOSOURCE INC. |
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| Product Specific References | Vissers L E., et al. (2011) Am J Hum Genet. 88 (5):608-15.; Kalujnaia S., et al. (2010) FASEB J. 24 (10):3981-91. |
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