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Glycogen Synthase 1 anticorps

Cet anticorps anti-Glycogen Synthase 1 est un anticorps Lapin Polyclonal détectant Glycogen Synthase 1 dans WB, ELISA, IHC, IF, IP et FACS. Adapté pour Humain, Souris et Rat.
N° du produit ABIN5701758

Aperçu rapide pour Glycogen Synthase 1 anticorps (ABIN5701758)

Antigène

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

Reactivité

  • 58
  • 36
  • 29
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
Humain, Souris, Rat

Hôte

  • 57
  • 2
Lapin

Clonalité

  • 43
  • 16
Polyclonal

Conjugué

  • 38
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
Cet anticorp Glycogen Synthase 1 est non-conjugé

Application

  • 38
  • 23
  • 15
  • 10
  • 8
  • 8
  • 6
  • 4
  • 2
  • 1
  • 1
Western Blotting (WB), ELISA, Immunohistochemistry (IHC), Immunofluorescence (IF), Immunoprecipitation (IP), Flow Cytometry (FACS)
  • Fonction

    GYS1 antibody

    Immunogène

    glycogen synthase 1 (muscle)

    Isotype

    IgG
  • Indications d'application

    Optimal working dilution should be determined by the investigator.

    Commentaires

    K-562 cells were subjected to SDS PAGE followed by western blot with FNab03736(GYS1 antibody) at dilution of 1:500

    Restrictions

    For Research Use only
  • Buffer

    PBS with 0.02 % sodium azide and 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.

    Conseil sur la manipulation

    Avoid repeated freeze / thaw cycles.

    Stock

    -20 °C

    Stockage commentaire

    -20°C for 12 months

    Date de péremption

    12 months
  • Antigène

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

    Autre désignation

    GYS1

    Sujet

    Synonyms: Glycogen [starch] synthase, muscle|Glycogen synthase 1|GYS1|GYS

    Background: 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. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.

    Poids moléculaire

    84 kDa

    ID gène

    2997

    UniProt

    P13807

    Pathways

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