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mEH Antibody (17): sc-135984

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Datasheets
  • mEH Antibody (17) is a mouse monoclonal IgG1 κ mEH antibody, cited in 8 publications, provided at 200 µg/ml
  • raised against amino acids 13-125 of mEH of human origin
  • recommended for detection of mEH of mouse, rat and human origin by WB, IP and IF
  • m-IgGκ BP-HRP is the preferred secondary detection reagent for mEH Antibody (17) for WB applications. This reagent is now offered in a bundle with mEH Antibody (17) (see ordering information below). For additional m-IgGκ BP conjugates see our complete list of Mouse IgG Binding Proteins.

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mEH Antibody (17) is a mouse monoclonal IgG1 kappa light chain antibody that detects mEH protein of mouse, rat, and human origin by western blotting (WB), immunoprecipitation (IP), and immunofluorescence (IF). anti-mEH antibody (17) is available as the non-conjugated form. mEH protein, also known as microsomal epoxide hydrolase, plays a crucial role in the detoxification of harmful compounds by catalyzing the hydrolysis of epoxides into less reactive and more water-soluble dihydrodiols, which can then be easily excreted from the body. This enzymatic process is vital for protecting cells from the potentially damaging effects of various endogenous and exogenous toxicants, including those derived from tobacco smoke. mEH protein is encoded by the EPHX1 gene, located on chromosome 1q42.12, and exhibits broad substrate specificity, allowing mEH protein to metabolize a wide range of substrates. Notably, polymorphisms in the EPHX1 gene have been associated with an increased risk of certain cancers, such as ovarian cancer and hepatocellular carcinoma, highlighting the importance of mEH in both metabolic processes and disease susceptibility.

For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.

Alexa Fluor® is a trademark of Molecular Probes Inc., OR., USA

LI-COR® and Odyssey® are registered trademarks of LI-COR Biosciences

mEH Antibody (17) References:

  1. Analysis of the EPHX1 113 polymorphism and GSTM1 homozygous null polymorphism and oral clefting associated with maternal smoking.  |  Hartsfield, JK., et al. 2001. Am J Med Genet. 102: 21-4. PMID: 11471167
  2. Inhibitors of soluble epoxide hydrolase attenuate vascular smooth muscle cell proliferation.  |  Davis, BB., et al. 2002. Proc Natl Acad Sci U S A. 99: 2222-7. PMID: 11842228
  3. Microsomal epoxide hydrolase polymorphism as a risk factor for ovarian cancer.  |  Lancaster, JM., et al. 1996. Mol Carcinog. 17: 160-2. PMID: 8944076
  4. The role of human glutathione transferases and epoxide hydrolases in the metabolism of xenobiotics.  |  Seidegård, J. and Ekström, G. 1997. Environ Health Perspect. 105 Suppl 4: 791-9. PMID: 9255563

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

mEH Antibody (17)

sc-135984
200 µg/ml
$316.00

mEH Antibody (17): m-IgGκ BP-HRP Bundle

sc-521315
200 µg Ab, 40 µg BP
$354.00

I am using mEH (17): sc-135984 for immunofluorescence, what dilution of this antibody should I use?

Asked by: jerojero
Thank you for your question. We recommend a starting dilution of 1:50. However, optimal antibody concentration should be determined by titration. Please find our full immunofluorescence protocol here: https://www.scbt.com/scbt/resources/protocols/immunofluorescence-cell-staining
Answered by: Technical Support
Date published: 2017-03-24
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Rated 3 out of 5 by from Provides strong bands for WBUsed at 1:200 dilution for mouse tissue lysates. Provided good strong bands for WB. However, some non-specific binding as well. Will need to be optimized.
Date published: 2018-03-22
Rated 5 out of 5 by from Excellent for westernsWe ran this Ab on western blot of WT and mEH null liver lysates. Blocked with 5% NFM, ran Ab in 1:200 in PBST with 1% BSA. We got clear bands in WT. No bands in the null mice. Clean background.
Date published: 2016-10-26
Rated 4 out of 5 by from Clear immunofluorescence cytoplasmic stainingClear immunofluorescence cytoplasmic staining in NIH/3T3 cells. -SCBT QC
Date published: 2015-03-11
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mEH Antibody (17) is rated 4.0 out of 5 by 4.
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