UROS protein (His tag) (80R-1823)
Purified recombinant Human UROS protein
Overview
Overview
Synonyms | Uroporphyrinogen III synthase protein, Uroporphyrinogen-III synthase protein |
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Species | Human |
Protein Type | Recombinant |
Applications | SDS-PAGE |
Images
Coomassie Blue stained SDS-PAGE of UROS protein (His tag) (80R-1823)
Figure annotation denotes ug of protein loaded and % gel used.
Specifications
Residues | 1-265 amino acids: MGSSHHHHHH SSGLVPRGSH MKVLLLKDAK EDDCGQDPYI RELGLYGLEA TLIPVLSFEF LSLPSFSEKL SHPEDYGGLI FTSPRAVEAA ELCLEQNNKT EVWERSLKEK WNAKSVYVVG NATASLVSKI GLDTEGETCG NAEKLAEYIC SRESSALPLL FPCGNLKREI LPKALKDKGI AMESITVYQT VAHPGIQGNL NSYYSQQGVP ASITFFSPSG LTYSLKHIQE LSGDNIDQIK FAAIGPTTAR ALAAQGLPVS CTAESPTPQA LATGIRKALQ PHGCC |
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Expression System | E.coli |
Grade & Purity | > 95% pure |
Molecular Weight | 30.7 kDa (285aa) confirmed by MALDI-TOF |
Tag/Conjugate | His tag |
Form & Buffer | Supplied as a liquid in 20mM Tris-HCl buffer, pH 8.0, containing 10% glycerol and 0.1M NaCl. |
Concentration | 1 mg/ml |
Storage & Safety
Storage | Store at 4 deg C for short term storage (1/2 weeks). Aliquot and store at -20 deg C or - 70 deg C for long term storage. Avoid repeated freeze/thaw cycles. |
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General Information
Biological Significance | UROS, also known as Uroporphyrinogen III synthase, is an enzyme involved in the fourth step of porphyrin metabolism, involved in the conversion of hydroxymethyl bilane into uroporphyrinogen III. Defects in this protein can cause molecular lesions that lead to the autosomal recessive Gunther disease, also known as congenital erythropoietic porphyria (CEP). Recombinant human UROS protein, fused to His-tag at N-terminus, was expressed in E. coli and purified by using conventional chromatography. |
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