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Glycogen Synthase 1 anticorps

Cet anticorps anti-Glycogen Synthase 1 est un anticorps Souris Monoclonal détectant Glycogen Synthase 1 dans WB, ELISA et FACS. Adapté pour Humain. Ce Primary Antibody a été cité dans 1 publication.
N° du produit ABIN969183

Aperçu rapide pour Glycogen Synthase 1 anticorps (ABIN969183)

Antigène

Voir toutes Glycogen Synthase 1 (GYS1) Anticorps
Glycogen Synthase 1 (GYS1) (Glycogen Synthase 1 (Muscle) (GYS1))

Reactivité

  • 56
  • 35
  • 28
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
Humain

Hôte

  • 56
  • 1
Souris

Clonalité

  • 42
  • 15
Monoclonal

Conjugué

  • 36
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
Cet anticorp Glycogen Synthase 1 est non-conjugé

Application

  • 36
  • 21
  • 16
  • 11
  • 9
  • 8
  • 5
  • 4
  • 2
  • 1
  • 1
Western Blotting (WB), ELISA, Flow Cytometry (FACS)

Clone

3A7
  • Fonction

    GYS1 Antibody

    Purification

    Ascitic fluid

    Immunogène

    Purified recombinant fragment of human GYS1 expressed in E. Coli.

    Isotype

    IgG1
  • Indications d'application

    ELISA: 1/10000

    FCM: 1/200 - 1/400

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Ascitic fluid containing 0.03 % sodium azide.

    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

    4 °C,-20 °C

    Stockage commentaire

    Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
  • Luttjeboer, Harada, Hughes, Johnson, Lilford, Mol: "Tubal flushing for subfertility." dans: Cochrane database of systematic reviews (Online), Issue 3, pp. CD003718, (2007) (PubMed).

  • Antigène

    Glycogen Synthase 1 (GYS1) (Glycogen Synthase 1 (Muscle) (GYS1))

    Autre désignation

    GYS1

    Sujet

    Glycogen synthase, skeletal muscle, the rate limiting enzyme of the insulin-induced glycogenesis. The protein encoded by this gene catalyzes the addition of glucose monomers to the growing glycogen molecule through the formation of alpha-1, 4-glycoside linkages. Mutations in this gene are associated with muscle glycogen storage disease. Muscle GS is expressed in several tissues.

    Poids moléculaire

    85 kDa

    ID gène

    2997

    UniProt

    P13807

    Pathways

    Signalisation PI3K-Akt, AMPK Signaling, Cellular Glucan Metabolic Process
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