EHHADH anticorps (AA 673-723)

N° du produit ABIN7451013

Détail du produit anti-EHHADH anticorps

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

Épitope: AA 673-723

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp EHHADH est non-conjugé

Application: Western Blotting (WB), Immunoprecipitation (IP)

Fonction: Rabbit anti-PBE Antibody, Affinity Purified

Homologie: Orangutan

Purification: Affinity Purified

Immunogène: between AA 673 and 723

Isotype: IgG

Information d'application

Indications d'application:

IP: 2 - 10 μg/mg lysate

WB: 1:500 - 1:2,500

Restrictions: For Research Use only

Stockage

Concentration: 1000 μg/mL

Buffer: Tris-citrate/phosphate buffer, pH 7 to 8 containing 0.09 % Sodium Azide

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: 4 °C

Date de péremption: 12 months

Détails sur EHHADH

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

Autre désignation: PBE (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: Background: Peroxisomal bifunctional enzyme (PBE) is one of the four enzymes of the peroxisomal beta-oxidation pathway. The N-terminal region of PBE contains enoyl-CoA hydratase activity while the C-terminal region contains 3-hydroxyacyl-CoA dehydrogenase activity. Defects in the PBE gene are a cause of peroxisomal disorders such as Zellweger syndrome [taken from NCBI Entrez Gene (Gene ID: 1962)].

ID gène: 1962

NCBI Accession: NP_001957

UniProt: Q08426

Pathways: Monocarboxylic Acid Catabolic Process