FA2H Antikörper (AA 95-170)

Produktnummer ABIN6140410

Produktdetails anti-FA2H Antikörper

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

Bindungsspezifität: AA 95-170

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser FA2H Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Sequenz: NEPVALEETQ KTDPAMEPRF KVVDWDKDLV DWRKPLLWQV GHLGEKYDEW VHQPVTRPIR LFHSDLIEGL SKTVWY

Kreuzreaktivität: Human, Ratte

Produktmerkmale: Polyclonal Antibodies

Aufreinigung: Affinity purification

Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 95-170 of human FA2H (NP_077282.3).

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB,1:500 - 1:2000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

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 -20°C. 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.,FA2H,FAAH,FAH1,FAXDC1,SCS7,SPG35,Signal Transduction,Endocrine & Metabolism,Lipid Metabolism,Neuroscience,Cell Type Marker,Neuron marker,Axon marker,FA2H

Molekulargewicht: 18 kDa/42 kDa

Gen-ID: 79152

UniProt: Q7L5A8