FA2H Antikörper

Produktnummer ABIN6292085

Produktdetails anti-FA2H Antikörper

Target: FA2H (Fatty Acid 2-Hydroxylase (FA2H))

Reaktivität: Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser FA2H Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Aufreinigung: Affinity purification

Immunogen: Recombinant protein of human FA2H

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:500 - 1:2000

Kommentare:

Detected in differentiating cultured keratinocytes (at protein level), Detected in epidermis and cultured keratinocytes, Highly expressed in brain and colon, Detected at lower levels in testis, prostate, pancreas and kidney

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 FA2H

Target: FA2H (Fatty Acid 2-Hydroxylase (FA2H))

Andere Bezeichnung: FA2H (FA2H Produkte)

Synonyme: FAAH antikoerper, FAH1 antikoerper, FAXDC1 antikoerper, SCS7 antikoerper, SPG35 antikoerper, RGD1310347 antikoerper, Wdr59 antikoerper, Faxdc1 antikoerper, G630055L08Rik antikoerper, MGC85470 antikoerper, MGC97767 antikoerper, cb1044 antikoerper, zgc:153777 antikoerper, fatty acid 2-hydroxylase antikoerper, fatty acid 2-hydroxylase L homeolog antikoerper, fatty acid hydroxylase antikoerper, FA2H antikoerper, Fa2h antikoerper, fa2h.L antikoerper, fa2h antikoerper, Tsp_11648 antikoerper, Ilyop_0703 antikoerper, Celly_1453 antikoerper, Weevi_1515 antikoerper, Fluta_1455 antikoerper, Mesop_3301 antikoerper

Hintergrund: This gene encodes a protein that catalyzes the synthesis of 2-hydroxysphingolipids, a subset of sphingolipids that contain 2-hydroxy fatty acids. Sphingolipids play roles in many cellular processes and their structural diversity arises from modification of the hydrophobic ceramide moiety, such as by 2-hydroxylation of the N-acyl chain, and the existence of many different head groups. Mutations in this gene have been associated with leukodystrophy dysmyelinating with spastic paraparesis with or without dystonia.

Molekulargewicht: 42.791 kDa

Gen-ID: 79152

UniProt: Q7L5A8