catalog number :
MBS8245670
products full name :
Anti-EPHX1 Antibody
products short name :
[EPHX1]
products name syn :
[EPHX; EPOX; Epoxide hydrolase 1; Epoxide hydratase; Microsomal epoxide hydrolase]
other names :
[epoxide hydrolase 1; Epoxide hydrolase 1; epoxide hydrolase 1; epoxide hydrolase 1; Epoxide hydratase; Microsomal epoxide hydrolase]
products gene name :
[EPHX1]
other gene names :
[EPHX1; EPHX1; MEH; EPHX; EPOX; HYL1; EPHX; EPOX]
uniprot entry name :
HYEP_HUMAN
reactivity :
Human, Mouse, Rat
specificity :
Recognizes endogenous levels of EPHX1 protein.
purity :
The antibody was purified by immunogen affinity chromatography.
form :
Liquid in 0.42% Potassium phosphate, 0.87% Sodium chloride, pH 7.3, 30% glycerol, and 0.01% sodium azide.
storage stability :
Shipped at 4 degree C. Upon delivery aliquot and store at -20 degree C for one year. Avoid freeze/thaw cycles.
tested application :
Western Blot (WB), Immunohistochemistry (IHC)
app notes :
WB: 1/500 - 1/2000; IHC: 1/50 - 1/200
image1 heading :
Western Blot (WB)
image2 heading :
Immunohistochemistry (IHC)
other info1 :
Source: Rabbit. Immunogen: Recombinant full length protein of human EPHX1
products description :
Rabbit polyclonal antibody to EPHX1
ncbi acc num :
NP_000111.1
ncbi gb acc num :
NM_000120.3
ncbi mol weight :
52,949 Da
ncbi pathways :
Aflatoxin B1 Metabolism Pathway (198808); Benzo(a)pyrene Metabolism Pathway (198911); Bile Secretion Pathway (193146); Bile Secretion Pathway (193095); Biological Oxidations Pathway (1270189); Chemical Carcinogenesis Pathway (673221); Chemical Carcinogenesis Pathway (673237); Metabolism Pathway (1269956); Metabolism Of Xenobiotics By Cytochrome P450 Pathway (83031); Metabolism Of Xenobiotics By Cytochrome P450 Pathway (425)
ncbi summary :
Epoxide hydrolase is a critical biotransformation enzyme that converts epoxides from the degradation of aromatic compounds to trans-dihydrodiols which can be conjugated and excreted from the body. Epoxide hydrolase functions in both the activation and detoxification of epoxides. Mutations in this gene cause preeclampsia, epoxide hydrolase deficiency or increased epoxide hydrolase activity. Alternatively spliced transcript variants encoding the same protein have been found for this gene.[provided by RefSeq, Dec 2008]
uniprot summary :
Ephx1: Biotransformation enzyme that catalyzes the hydrolysis of arene and aliphatic epoxides to less reactive and more water soluble dihydrodiols by the trans addition of water. In some populations, the high activity haplotype tyr113/his139 is overrepresented among women suffering from pregnancy-induced hypertension (pre-eclampsia) when compared with healthy controls. Defects in EPHX1 are a cause of familial hypercholanemia (FHCA). FHCA is a disorder characterized by elevated serum bile acid concentrations, itching, and fat malabsorption. Belongs to the peptidase S33 family. Protein type: EC 3.3.2.9; Membrane protein, integral; Xenobiotic Metabolism - metabolism by cytochrome P450; Hydrolase. Chromosomal Location of Human Ortholog: 1q42.1. Cellular Component: endoplasmic reticulum membrane; integral to membrane. Molecular Function: cis-stilbene-oxide hydrolase activity; epoxide hydrolase activity. Biological Process: aromatic compound catabolic process; response to organic cyclic substance; response to toxin; xenobiotic metabolic process. Disease: Hypercholanemia, Familial; Preeclampsia/eclampsia 1