| 产品详情 |
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| Product Name | HMBS, 1-361aa, Human, His tag, E Coli |
| Description | MW: 41.9kDa (385aa) confirmed by MALDI-TOF. Purity >95% by SDS-PAGE. Porphobilinogen deaminase, also known as HMBS, is a member of the hydroxymethylbilane synthase superfamily. It is a cytoplasmic enzyme found in the heme synthesis pathway. Deficiency of HMBS causes errors in pyrrole metabolism which in turn leads to an inherited autosomal disorder called acute intermittent porphyria (AIP) which is characterized by acute attacks of neurological dysfunctions with hypertension, tachycardia, periph |
| Size | 0.1 mg, 0.5 mg |
| Concentration | 1 mg/ml (determined by Bradford assay) |
| Applications | SDS-PAGE |
| Other Names | [Porphobilinogen deaminase; PBG-D; PBGD; PORC; uPS] |
| Gene, Accession, CAS # | HMBS, Gene ID: 3145, Accession: NP_000181 |
| Catalog # | MBS204406 |
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| Order / More Info | HMBS, 1-361aa, Human, His tag, E Coli from MYBIOSOURCE INC. |
| Product Specific References | Schneider Yin X., et al. (2004) J Inherit Metab Dis. 625-631:471-474.; Sheppard L., et al. (1995) Paediatr Anaesth. 15:426-428.; |
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