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GCSH anticorps

Cet anticorps anti-GCSH est un anticorps Lapin Polyclonal détectant GCSH dans ELISA et IHC. Adapté pour Humain, Souris et Rat.
N° du produit ABIN7247492

Aperçu rapide pour GCSH anticorps (ABIN7247492)

Antigène

Voir toutes GCSH Anticorps
GCSH (Glycine Cleavage System H Protein (GCSH))

Reactivité

  • 39
  • 10
  • 10
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Humain, Souris, Rat

Hôte

  • 37
  • 2
Lapin

Clonalité

  • 38
  • 1
Polyclonal

Conjugué

  • 13
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp GCSH est non-conjugé

Application

  • 32
  • 14
  • 13
  • 13
  • 3
  • 3
  • 3
  • 2
  • 1
  • 1
ELISA, Immunohistochemistry (IHC)
  • Attributs du produit

    Polyclonal Antibody

    Purification

    Antigen affinity purification

    Immunogène

    Fusion protein of human GCSH

    Isotype

    IgG
  • Indications d'application

    IHC 1:50-1:200, ELISA 1:5000-1:10000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1.02 mg/mL

    Buffer

    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

    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

    GCSH (Glycine Cleavage System H Protein (GCSH))

    Autre désignation

    GCSH

    Sujet

    Degradation of glycine is brought about by the glycine cleavage system, which is composed of four mitochondrial protein components: P protein (a pyridoxal phosphate-dependent glycine decarboxylase), H protein (a lipoic acid-containing protein), T protein (a tetrahydrofolate-requiring enzyme), and L protein (a lipoamide dehydrogenase). The protein encoded by this gene is the H protein, which transfers the methylamine group of glycine from the P protein to the T protein. Defects in this gene are a cause of nonketotic hyperglycinemia (NKH). Two transcript variants, one protein-coding and the other probably not protein-coding,have been found for this gene. Also, several transcribed and non-transcribed pseudogenes of this gene exist throughout the genome.

    UniProt

    P23434
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