EHHADH antibody

Catalog No. ABIN6292474

Product Details anti-EHHADH Antibody

Target: EHHADH (Enoyl-CoA, Hydratase/3-Hydroxyacyl CoA Dehydrogenase (EHHADH))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This EHHADH antibody is un-conjugated

Application: Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)

Purification: Affinity purification

Immunogen: Recombinant protein of human EHHADH

Isotype: IgG

Application Details

Application Notes: WB 1:500 - 1:2000
IHC 1:50 - 1:200
IF 1:50 - 1:200

Comment:

Liver and kidney, Strongly expressed in the terminal segments of the proximal tubule, Lower amounts seen in the brain

Restrictions: For Research Use only

Handling

Buffer: PBS with 0.02 % sodium azide, 50 % glycerol,  pH 7.3.

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Store at -20C. Avoid freeze / thaw cycles.

Target Details for EHHADH

Target: EHHADH (Enoyl-CoA, Hydratase/3-Hydroxyacyl CoA Dehydrogenase (EHHADH))

Alternative Name: EHHADH (EHHADH Products)

Synonyms: ECHD antibody, L-PBE antibody, LBFP antibody, LBP antibody, PBFE antibody, 1 antibody, Lbp antibody, MEF antibody, Mfe antibody, Mfe1 antibody, Pbe antibody, Pbfe antibody, perMFE-1 antibody, 1300002P22Rik antibody, HD antibody, MFP antibody, MFP1 antibody, zgc:77526 antibody, Ehhadh antibody, enoyl-CoA hydratase and 3-hydroxyacyl CoA dehydrogenase antibody, enoyl-CoA, hydratase/3-hydroxyacyl CoA dehydrogenase antibody, enoyl-Coenzyme A, hydratase/3-hydroxyacyl Coenzyme A dehydrogenase antibody, peroxisomal bifunctional enzyme-like antibody, EHHADH antibody, ehhadh antibody, Ehhadh antibody, LOC100135519 antibody

Background: The protein encoded by this gene is a bifunctional enzyme and is one of the four enzymes of the peroxisomal beta-oxidation pathway. The N-terminal region of the encoded protein contains enoyl-CoA hydratase activity while the C-terminal region contains 3-hydroxyacyl-CoA dehydrogenase activity. Defects in this gene are a cause of peroxisomal disorders such as Zellweger syndrome. Two transcript variants encoding different isoforms have been found for this gene.

Molecular Weight: 79.495 kDa

Gene ID: 1962

UniProt: Q08426

Pathways: Monocarboxylic Acid Catabolic Process