UGT1A9 rabbit pAb

UGT1A9 rabbit pAb

AO-06-ES12431-50

UGT1A9 rabbit pAb 50μL

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Antibody Product Overview

ELK.NoES12431
Product nameUGT1A9 rabbit pAb
ReactivityHuman; Mouse
ApplicationsWB
Other nameUDP-glucuronosyltransferase 1-9 (UDPGT 1-9) (UGT1*9) (UGT1-09) (UGT1.9) (EC 2.4.1.17) (UDP-glucuronosyltransferase 1-I) (UGT-1I) (UGT1I) (UDP-glucuronosyltransferase 1A9) (lugP4)
Size50μL
Unit price ($)148
Human gene ID54600
Human Swiss-ProtO60656
SourceRabbit
IsotypeIgG
TargetUGT1A9
Fields>>Pentose and glucuronate interconversions;>>Ascorbate and aldarate metabolism;>>Steroid hormone biosynthesis;>>Retinol metabolism;>>Porphyrin metabolism;>>Metabolism of xenobiotics by cytochrome P450;>>Drug metabolism - cytochrome P450;>>Drug metabolism - other enzymes;>>Metabolic pathways;>>Biosynthesis of cofactors;>>Bile secretion;>>Chemical carcinogenesis - DNA adducts;>>Chemical carcinogenesis - receptor activation
Gene nameUGT1A9 GNT1 UGT1
Protein nameUGT1A9
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID394434
Mouse gene linkView Mouse Gene
Mouse Swiss-ProtQ62452
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID
Rat gene link
Rat Swiss-Prot
Rat Swiss link
ImmunogenSynthesized peptide derived from human UGT1A9 AA range: 390-440
SpecificityThis antibody detects endogenous levels of UGT1A9 at Human/Mouse
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.11% sodium azide.
ClonalityPolyclonal
DilutionWB 1:500-2000
PurificationThe antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)
Observed band (KD)75kD
BackgroundThis 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 enzyme encoded by this gene is active on phenols. [provided by RefSeq, Jul 2008],
Functionalternative products:A number of isoforms are produced. The different isozymes have a different N-terminal domain and a common C-terminal domain of 245 residues,alternative products:A number of isoforms may be produced. Isoforms have a different N-terminal domain and a common C-terminal domain of 245 residues,catalytic activity:UDP-glucuronate + acceptor = UDP + acceptor beta-D-glucuronoside.,caution:The sequence shown here is derived from an Ensembl automatic analysis pipeline and should be considered as preliminary data.,disease:Defects in UGT1A1 are the cause of Crigler-Najjar syndrome type I (CN-I) [MIM:218800]. CN-I patients have severe hyperbilirubinemia and usually die of kernicterus (bilirubin accumulation in the basal ganglia and brainstem nuclei) within the first year of life. CN-I inheritance is autosomal recessive.,disease:Defects in UGT1A1 are the cause of Crigler-Najjar syn
Subcellular locationEndoplasmic reticulum membrane ; Single-pass membrane protein .
Expression[Isoform 1]: Expressed in liver, kidney, colon, esophagus and small intestine. ; [Isoform 2]: Expressed in liver, kidney, colon, esophagus and small intestine.

Additional Images

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Western blot analysis of lysates from Hela cells, primary antibody was diluted at 1:1000, 4°over night
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: AO-06-ES12431-50
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