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FA2H anticorps (AA 95-170)

Cet anticorps anti-FA2H est un anticorps Lapin Polyclonal détectant FA2H dans WB. Adapté pour Humain.
N° du produit ABIN6140410

Aperçu rapide pour FA2H anticorps (AA 95-170) (ABIN6140410)

Antigène

Voir toutes FA2H Anticorps
FA2H (Fatty Acid 2-Hydroxylase (FA2H))

Reactivité

  • 30
  • 20
  • 12
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Humain

Hôte

  • 24
  • 6
Lapin

Clonalité

  • 26
  • 4
Polyclonal

Conjugué

  • 18
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp FA2H est non-conjugé

Application

  • 23
  • 12
  • 10
  • 2
  • 1
Western Blotting (WB)
  • Épitope

    • 7
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 95-170

    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
  • Indications d'application

    WB,1:500 - 1:2000

    Restrictions

    For Research Use only
  • 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.
  • Antigène

    FA2H (Fatty Acid 2-Hydroxylase (FA2H))

    Autre désignation

    FA2H

    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
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