| 产品详情 |
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| Product Name | IMPAD1, human recombinant |
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| Description | IMPAD1, also known as Inositol monophosphatase 3, 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 His-tag at N-terminus, was expressed in E.coli and purified by conventional chromatography, after refolding of the isolated inclusion bodies in a renaturation buffer. MW: 37.6 kDa (349 aa, 34-359 aa + His Tag). Purity ≥90% |
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| Size | 10 µg |
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| Concentration | 0.25 mg/ml |
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| Applications | RUO |
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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: Q9NX62 |
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| Catalog # | 7812-10 |
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| Order / More Info | IMPAD1, human recombinant from BIOVISION, INC. |
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| Product Specific References | n/a |
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