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Glycogenin 1 anticorps (AA 251-350) (Biotin)

Cet anticorps anti-Glycogenin 1 est un anticorps Lapin Polyclonal détectant Glycogenin 1 dans WB, ELISA, IHC (p) et IHC (fro). Adapté pour Humain.
N° du produit ABIN752190

Aperçu rapide pour Glycogenin 1 anticorps (AA 251-350) (Biotin) (ABIN752190)

Antigène

Voir toutes Glycogenin 1 (GYG1) Anticorps
Glycogenin 1 (GYG1)

Reactivité

  • 27
  • 4
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
Humain

Hôte

  • 22
  • 5
Lapin

Clonalité

  • 24
  • 3
Polyclonal

Conjugué

  • 14
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp Glycogenin 1 est conjugé à/à la Biotin

Application

  • 26
  • 14
  • 14
  • 9
  • 6
  • 3
  • 3
  • 1
  • 1
Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
  • Épitope

    • 15
    • 3
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 251-350

    Homologie

    Human,Mouse,Rat,Dog,Cow,Sheep,Pig

    Purification

    Purified by Protein A.

    Immunogène

    KLH conjugated synthetic peptide derived from human Gyg1

    Isotype

    IgG
  • Indications d'application

    WB 1:300-5000
    IHC-P 1:200-400
    IHC-F 1:100-500

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 μg/μL

    Buffer

    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

    Agent conservateur

    ProClin

    Précaution d'utilisation

    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

    Stock

    -20 °C

    Stockage commentaire

    Store at -20°C for 12 months.

    Date de péremption

    12 months
  • Antigène

    Glycogenin 1 (GYG1)

    Autre désignation

    GYG1

    Sujet

    Synonyms: Glycogenin, Glycogenin1, GYG 1, GYG, GYG1, GLYG_HUMAN.

    Background: This gene encodes a member of the glycogenin family. Glycogenin is a glycosyltransferase that catalyzes the formation of a short glucose polymer from uridine diphosphate glucose in an autoglucosylation reaction. This reaction is followed by elongation and branching of the polymer, catalyzed by glycogen synthase and branching enzyme, to form glycogen. This gene is expressed in muscle and other tissues. Mutations in this gene result in glycogen storage disease XV. This gene has pseudogenes on chromosomes 1, 8 and 13 respectively. Alternatively spliced transcript variants encoding different isoforms have been identified.[provided by RefSeq, Sep 2010].

    ID gène

    2992

    Pathways

    Cellular Glucan Metabolic Process
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