EHHADH Antikörper

Produktnummer ABIN6292474

Produktdetails anti-EHHADH Antikörper

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

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser EHHADH Antikörper ist unkonjugiert

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

Aufreinigung: Affinity purification

Immunogen: Recombinant protein of human EHHADH

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:500 - 1:2000
IHC 1:50 - 1:200
IF 1:50 - 1:200

Kommentare:

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

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

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

Konservierungsmittel: Sodium azide

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

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20C. Avoid freeze / thaw cycles.

Details zu EHHADH

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

Andere Bezeichnung: EHHADH (EHHADH Produkte)

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

Hintergrund: 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.

Molekulargewicht: 79.495 kDa

Gen-ID: 1962

UniProt: Q08426

Pathways: Monocarboxylic Acid Catabolic Process