FA2H anticorps (AA 95-170)

N° du produit ABIN6140410

Détail du produit anti-FA2H anticorps

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

Épitope: AA 95-170

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp FA2H est non-conjugé

Application: Western Blotting (WB)

Séquence: NEPVALEETQ KTDPAMEPRF KVVDWDKDLV DWRKPLLWQV GHLGEKYDEW VHQPVTRPIR LFHSDLIEGL SKTVWY

Réactivité croisée: Humain, Rat

Attributs du produit: Polyclonal Antibodies

Purification: Affinity purification

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

Isotype: IgG

Information d'application

Indications d'application: WB,1:500 - 1:2000

Restrictions: For Research Use only

Stockage

Format: Liquid

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 -20°C. Avoid freeze / thaw cycles.

Détails sur FA2H

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

Autre désignation: FA2H (FA2H Produits)

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

Sujet: 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

Poids moléculaire: 18 kDa/42 kDa

ID gène: 79152

UniProt: Q7L5A8