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PGK1 anticorps

Cet anticorps anti-PGK1 est un anticorps Lapin Polyclonal détectant PGK1 dans IHC. Adapté pour Humain, Souris et Rat.
N° du produit ABIN7008583

Aperçu rapide pour PGK1 anticorps (ABIN7008583)

Antigène

Voir toutes PGK1 Anticorps
PGK1 (Phosphoglycerate Kinase 1 (PGK1))

Reactivité

  • 77
  • 42
  • 22
  • 5
  • 5
  • 4
  • 4
  • 4
  • 4
  • 3
  • 3
  • 3
  • 2
  • 1
  • 1
Humain, Souris, Rat

Hôte

  • 67
  • 12
  • 1
  • 1
Lapin

Clonalité

  • 58
  • 20
Polyclonal

Conjugué

  • 52
  • 6
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
Cet anticorp PGK1 est non-conjugé

Application

  • 63
  • 35
  • 33
  • 18
  • 15
  • 12
  • 9
  • 5
  • 4
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Immunohistochemistry (IHC)
  • Attributs du produit

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogène

    Recombinant fusion protein of human PGK1 (NP_000282.1).

    Isotype

    IgG
  • Indications d'application

    IHC 1:50-1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    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

    PGK1 (Phosphoglycerate Kinase 1 (PGK1))

    Autre désignation

    PGK1

    Sujet

    The protein encoded by this gene is a glycolytic enzyme that catalyzes the conversion of 1,3-diphosphoglycerate to 3-phosphoglycerate. The encoded protein may also act as a cofactor for polymerase alpha. Additionally, this protein is secreted by tumor cells where it participates in angiogenesis by functioning to reduce disulfide bonds in the serine protease, plasmin, which consequently leads to the release of the tumor blood vessel inhibitor angiostatin. The encoded protein has been identified as a moonlighting protein based on its ability to perform mechanistically distinct functions. Deficiency of the enzyme is associated with a wide range of clinical phenotypes hemolytic anemia and neurological impairment. Pseudogenes of this gene have been defined on chromosomes 19, 21 and the X chromosome.

    ID gène

    5230

    UniProt

    P00558

    Pathways

    Cellular Glucan Metabolic Process
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