EPHX1 Antibody
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货号:CSB-PA007734LA01HU
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规格:¥440
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促销:
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图片:
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Western blot
All lanes: EPHX1 antibody at 2µg/ml + Hela whole cell lysate
Secondary
Goat polyclonal to rabbit IgG at 1/10000 dilution
Predicted band size: 53 kDa
Observed band size: 53 kDa -
Immunohistochemistry of paraffin-embedded human pancreatic tissue using CSB-PA007734LA01HU at dilution of 1:100
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Immunohistochemistry of paraffin-embedded human prostate tissue using CSB-PA007734LA01HU at dilution of 1:100
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其他:
产品详情
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产品名称:Rabbit anti-Homo sapiens (Human) EPHX1 Polyclonal antibody
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Uniprot No.:P07099
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基因名:EPHX1
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别名:EPHX 1 antibody; EPHX antibody; Ephx1 antibody; EPOX antibody; Epoxide hydratase antibody; Epoxide hydrolase 1 antibody; Epoxide hydrolase 1 microsomal (xenobiotic) antibody; Epoxide hydroxylase 1 antibody; Epoxide hydroxylase 1 microsomal (xenobiotic) antibody; HYEP_HUMAN antibody; HYL1 antibody; MEH antibody; Microsomal epoxide hydrolase antibody
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宿主:Rabbit
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反应种属:Human
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免疫原:Recombinant Human Epoxide hydrolase 1 protein (1-455AA)
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免疫原种属:Homo sapiens (Human)
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标记方式:Non-conjugated
本页面中的产品,EPHX1 Antibody (CSB-PA007734LA01HU),的标记方式是Non-conjugated。对于EPHX1 Antibody,我们还提供其他标记。见下表:
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克隆类型:Polyclonal
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抗体亚型:IgG
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纯化方式:>95%, Protein G purified
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浓度:It differs from different batches. Please contact us to confirm it.
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保存缓冲液:Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, PH 7.4 -
产品提供形式:Liquid
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应用范围:ELISA, WB, IHC
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推荐稀释比:
Application Recommended Dilution WB 1:500-1:5000 IHC 1:20-1:200 -
Protocols:
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储存条件:Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
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货期:Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
相关产品
靶点详情
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功能: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. Plays a role in the metabolism of endogenous lipids such as epoxide-containing fatty acids. Metabolizes the abundant endocannabinoid 2-arachidonoylglycerol (2-AG) to free arachidonic acid (AA) and glycerol.
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基因功能参考文献:
- The substrate specificity of microsomal epoxide hydrolase should therefore be expanded to include not only epoxides but also the oxetanyl ring system present in AZD1979. PMID: 27256986
- EPHX1 variants were significantly associated with higher metabolic ratio of carbamazepine PMID: 27276192
- Single nucleotide polymorphisms in EPHX1, GSTP1, SERPINE2, and TGFB1 contributing to the quantitative traits of chronic obstructive pulmonary disease in Chinese Han population. PMID: 27193053
- This study showed that polymorphisms of EPHX1 and VKORC1L1 could be determinants of stable warfarin doses. PMID: 29054760
- The Tyr113His T/C variant of rs1051740 and very slow phenotype alters EPHX1, miR-26b-5p and miR-1207-5p expression, and contributes towards low blood iron levels and low birthweights. PMID: 28789952
- Structural characterization of human microsomal epoxide hydrolase by combined homology modeling, molecular dynamics simulations, and molecular docking calculations has been reported. PMID: 28120429
- Y113H polymorphism in EPHX1 gene contributed to increased susceptibility to COPD in the Kazakhstan population. PMID: 28464990
- EPHX1 polymorphisms were not associated with sporadic colorectal neoplasms. PMID: 28018104
- This study demonstrated that two SNPs might play roles in the process of nicotine metabolism and abstinence, rs1051740 being more important; and EPHX SNPs (rs1051740 and rs2234922) are associated with the effectiveness of Nicotine Replacement Therapy . PMID: 27783326
- No association was found between EPHX1 and COPD; however, a minor effect of EPHX1 on COPD risk was not completely excluded. PMID: 27173271
- The SCN1A IVS5-91G>A SNP is associated with susceptibility to epilepsy. SNPs in EPHX1 gene are influencing CBZ metabolism and disposition PMID: 26555147
- In conclusion, GSTs, EPHX1, and XPD are potential genetic factors for arsenic-induced skin cancers. The roles of these genes for arsenic-induced skin carcinogenesis need to be further evaluated. PMID: 26295053
- the EPHX1 Tyr113His polymorphism may be a risk factor for lung cancer in Asians, whereas it may be a decreased risk factor among Caucasians. However, this polymorphism was not found to be associated with breast cancer. PMID: 25222243
- To be poly(ADP-ribose)polymerase-1 (PARP-1) bound to the EPHX1 proximal promoter. PMID: 25992604
- Polymorphism in the EPHX1 gene may have a significant role in differential responses to treatment with N-acetylcysteine in patients with COPD. PMID: 25999707
- This review and meta-analysis suggests that EPHX1 Tyr113His polymorphism may be a risk factor for Head and Neck Cancer, while the EPHX1 His139Arg polymorphism has no association with Head and Neck Cancer risk. PMID: 25923690
- Studies suggest that the presence of microsomal epoxide hydrolase 1 (EPHX1) single nucleotide polymorphisms (SNPs) may significantly affect the risk of lung, upper aerodigestive tract, breast, bladder, and ovarian carcinomas. PMID: 26216302
- the genetic associations exist between mEH polymorphisms and lung cancer susceptibility in Asian populations PMID: 25312477
- These results demonstrate that 2-AG is an endogenous substrate for EPHX1, a potential role of EPHX1 in the endocannabinoid signaling and a new AA biosynthetic pathway. PMID: 24958911
- EPHX1 rs2292566 polymorphism may affect the maintenance dose of warfarin in Caucasians. PMID: 25629049
- His/His genotype of EPHX1 Tyr113His polymorphism is a risk factor for developing caner for Asian and mixed population, while no evidence was found for the association between the EPHX1 His139Arg polymorphism and increased cancer risk. PMID: 25261893
- EPHX1 Tyr113His and His139Arg polymorphism are not associated with esophageal cancer risk. PMID: 25714851
- This meta-analysis suggests that EPHX1 Tyr113His polymorphism contributes to HCC risk. PMID: 26065263
- No clear effect is evident for EPHX1 polymorphisms for different radon concentrations on the risk of lung cancer. PMID: 24852519
- Review/Meta-analysis: suggest p.Tyr113His and p.His139Arg polymorphisms in EPHX1 may not be associated with esophageal cancer development. PMID: 24803829
- This study provides direct evidence that methylation plays an important role in PCOS and demonstrates a novel role for EPHX1 in female reproduction. PMID: 24505354
- Meta-analysis showed that the Tyr113His polymorphism was a stronger power trend towards risk for esophageal cancer using a recessive model PMID: 24615030
- The association of EPHX1 polymorphism with the HELLP syndrome and eclampsia may hint to EPHX being a further key player in the pathogenesis of preeclampsia. PMID: 24013430
- Results suggest that Exons 3 and 4 polymorphisms of the mEH gene may contribute to lung cancer susceptibility through disturbed antioxidant balance. PMID: 23928928
- The C allele and C-G diplotype of EPHX1 may play important roles in increasing the risk of CBZ-SJS/toxic epidermal necrolysis development of epilepsy in Chinese Han patients. PMID: 24861996
- Chinese epilepsy patients with variant EPHX1 c.416A>G genotype have higher plasma carbamazepine concentrations compared to those with the wild type genotype. PMID: 24125961
- No evidence of an association of EPHX1 Tyr113His or His139Arg polymorphisms with risk for development of esophageal cancer. [Meta-analysis] PMID: 24222229
- EPHX1 genetic polymorphisms were not associated with the risk of HCC. PMID: 23955801
- The study showed that microsomal epoxide hydrolase exon 3 113Tyr-139Arg was associated with gastric cancer in presence of H. pylori, though in its absence, it appeared to be protective. PMID: 23580125
- Sp1 and Sp3 are functionally involved as transcriptional integrators regulating the basal expression of the derived microsomal epoxide hydrolase E1b variant transcript. PMID: 24315822
- Genotype frequencies for EPHX1 polymorphisms did not show any correlation with lymphoma. PMID: 23651475
- This meta-analysis suggests that EPHX1 His139Arg polymorphism is associated with decreased risk of esophageal cancer in Caucasians. PMID: 23681797
- There is substantial evidence that mEH polymorphisms interact synergistically with other genes and the environment to modulate risk of HCC PMID: 23451147
- findings suggest that benzene exposure may be associated with hypermethylation in ERCC3, and that genetic variants in EPHX1 may play an important role in epigenetic changes and hematotoxicity among benzene-exposed workers PMID: 23797950
- This is the first report that examined HIF1A polymorphisms in chronic obstructive pulmonary disease and demonstrated a possible role of HIF-1alpha in COPD, as well as GSTP1 and EPHX1. PMID: 21651746
- EPHX1 transcript, termed E1-b', drives EPHX1 expression primarily in the ovary. PMID: 23564882
- EPHX1 gene polymorphisms and haplotypes are associated with an increased risk for alcoholism in the Kota Indian population PMID: 22257321
- minor Tyr113 allele of mEPHX1 polymorphism had a higher risk of type 2 diabetes mellitus PMID: 22555758
- Microsomal epoxide hydrolase 1 T113C polymorphism is associated with lung cancer. PMID: 23378225
- the maternal EPHX1 rs1051740 genotype (RR = 3.26, P = .01) was associated with medulloblastoma risk. PMID: 22994552
- Meta-analyses of available data supported the concept of EPHX1 A139G polymorphism as a genetic susceptibility factor for lung cancer PMID: 23055191
- EPHX1 gene polymorphisms and haplotypes were not involved in the susceptibility to oral cancer in South Indian subjects. PMID: 21453055
- EPHX1 Tyr113His polymorphism may be not associated with CRC development PMID: 22928041
- Study analyzed the association between four SNPs in the EPHX1 and EPHX2 and the risk of oligozoospermia and asthenospermia; rs1051740, rs2234922 and rs751141 were not associated with oligozoospermia and asthenospermia and rs1042064 was a protective factor in idiopathic male infertility. PMID: 22986331
- microsomal epoxide hydrolase polymorphism is associated with chromosomal instability of 1,3-butadiene exposed workers. PMID: 22156006
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相关疾病:Familial hypercholanemia (FHCA)
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亚细胞定位:Microsome membrane; Single-pass type III membrane protein. Endoplasmic reticulum membrane; Single-pass type III membrane protein.
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蛋白家族:Peptidase S33 family
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组织特异性:Found in liver.
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数据库链接:
HGNC: 3401
OMIM: 132810
KEGG: hsa:2052
STRING: 9606.ENSP00000272167
UniGene: Hs.89649
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