EHHADH anticorps

N° du produit ABIN6292474

Détail du produit anti-EHHADH anticorps

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

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp EHHADH est non-conjugé

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

Purification: Affinity purification

Immunogène: Recombinant protein of human EHHADH

Isotype: IgG

Information d'application

Indications d'application: WB 1:500 - 1:2000
IHC 1:50 - 1:200
IF 1:50 - 1:200

Commentaires:

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

Restrictions: For Research Use only

Stockage

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

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Store at -20C. Avoid freeze / thaw cycles.

Détails sur EHHADH

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

Autre désignation: EHHADH (EHHADH Produits)

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

Sujet: 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.

Poids moléculaire: 79.495 kDa

ID gène: 1962

UniProt: Q08426

Pathways: Monocarboxylic Acid Catabolic Process