Recombinant Human UGT1A1, MYC/DDK-tagged

Cat.No. : UGT1A1-26H
Product Overview : Recombinant Human UGT1A1, fused with C-terminal MYC/DDK, was expressed in HEK293 cells.
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Description : This gene encodes a UDP-glucuronosyltransferase, an enzyme of the glucuronidation pathway that transforms small lipophilic molecules, such as steroids, bilirubin, hormones, and drugs, into water-soluble, excretable metabolites. This gene is part of a complex locus that encodes several UDP-glucuronosyltransferases. The locus includes thirteen unique alternate first exons followed by four common exons. Four of the alternate first exons are considered pseudogenes. Each of the remaining nine 5' exons may be spliced to the four common exons, resulting in nine proteins with different N-termini and identical C-termini. Each first exon encodes the substrate binding site, and is regulated by its own promoter. The preferred substrate of this enzyme is bilirubin, although it also has moderate activity with simple phenols, flavones, and C18 steroids. Mutations in this gene result in Crigler-Najjar syndromes types I and II and in Gilbert syndrome.
Source : HEK293 cells
Species : Human
Tag : MYC/DDK
Molecular Mass : 57.1 kDa
Purity : > 80% as determined by SDS-PAGE and Coomassie blue staining
Concentration : >50 ug/mL as determined by microplate BCA method
Storage Buffer : 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10% glycerol.
Gene Name : UGT1A1 UDP glucuronosyltransferase 1 family, polypeptide A1 [ Homo sapiens (human) ]
Official Symbol : UGT1A1
Synonyms : UGT1A1; UDP glucuronosyltransferase 1 family, polypeptide A1; GNT1; UGT1; UDPGT; UGT1A; HUG-BR1; BILIQTL1; UDPGT 1-1; UDP-glucuronosyltransferase 1-1; UDP glycosyltransferase 1 family, polypeptide A1; UDP-glucuronosyltransferase 1-A; UDP-glucuronosyltransferase 1A1; UGT-1A; UGT1*1; UGT1-01; UGT1.1; bilirubin UDP-glucuronosyltransferase 1-1; bilirubin UDP-glucuronosyltransferase isozyme 1; bilirubin-specific UDPGT isozyme 1; NP_000454.1; EC 2.4.1.17
Gene ID : 54658
mRNA Refseq : NM_000463
Protein Refseq : NP_000454
MIM : 191740
UniProt ID : P22309
Chromosome Location : 2q37
Pathway : AhR pathway; Chemical carcinogenesis; Defective GSS causes Glutathione synthetase deficiency (GSS deficiency); Defective MAT1A causes Methionine adenosyltransferase deficiency (MATD)
Function : enzyme binding; enzyme inhibitor activity; NOT glucuronosyltransferase activity; glucuronosyltransferase activity

For Research Use Only. Not intended for any clinical use. No products from Creative BioMart may be resold, modified for resale or used to manufacture commercial products without prior written approval from Creative BioMart.

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08/12/2022

    The product was kept in perfect condition and delivered on time so that I got the perfect product in the shortest time possible.

    05/14/2022

      Customer service contacted me in a timely manner and helped me solve a lot of problems that arose in my experiments.

      Q&As (5)

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      What is the function of UGT1A1? 07/14/2022

      UGT1A1 converts lipophilic small molecules, such as drugs, into water-soluble and excretable metabolites.

      What is the relationship between bilirubin and UGT1A1? 01/24/2022

      Bilirubin is a binding substrate for UGT1A1 and UGT1A1 is involved in bilirubin metabolism.

      What diseases is UGT1A1 involved in? 11/23/2021

      UGT1A1 is involved in lung cancer, colorectal cancer and hyperbilirubinemia, among other diseases.

      Where is UGT1A1 mainly expressed? 03/11/2021

      UGT1A1 is mainly expressed in the liver.

      What are the effects of mutations in the UGT1A1 gene? 02/09/2021

      Mutations in the UGT1A1 gene prevent the glucuronidation of free bilirubin and reduces bilirubin metabolism and increases serum free bilirubin levels.

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