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SGCE anticorps (AA 1-317)

Cet anticorps Lapin Polyclonal détecte spécifiquement SGCE dans WB, ELISA, IF et IP. Il présente une réactivité envers Humain, Souris et Rat.
N° du produit ABIN5704723

Aperçu rapide pour SGCE anticorps (AA 1-317) (ABIN5704723)

Antigène

Voir toutes SGCE Anticorps
SGCE (Sarcoglycan, epsilon (SGCE))

Reactivité

  • 25
  • 22
  • 20
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Humain, Souris, Rat

Hôte

  • 38
  • 2
Lapin

Clonalité

  • 40
Polyclonal

Conjugué

  • 17
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp SGCE est non-conjugé

Application

  • 30
  • 13
  • 13
  • 8
  • 6
  • 5
  • 4
  • 2
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Immunofluorescence (IF), Immunoprecipitation (IP)
  • Épitope

    • 15
    • 4
    • 4
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 1-317

    Fonction

    SGCE antibody

    Immunogène

    Immunogen sequence: 1-317aa

    Immunogen: sarcoglycan, epsilon

    Isotype

    IgG
  • Indications d'application

    Optimal working dilution should be determined by the investigator.

    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

    SGCE (Sarcoglycan, epsilon (SGCE))

    Autre désignation

    SGCE

    Sujet

    Synonyms: Epsilon-sarcoglycan (Epsilon-SG)|SGCE|ESG

    Background: This gene encodes the epsilon member of the sarcoglycan family. Sarcoglycans are transmembrane proteins that are components of the dystrophin-glycoprotein complex, which link the actin cytoskeleton to the extracellular matrix. Unlike other family members which are predominantly expressed in striated muscle, the epsilon sarcoglycan is more broadly expressed. Mutations in this gene are associated with myoclonus-dystonia syndrome. This gene is imprinted, with preferential expression from the paternal allele. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. A pseudogene associated with this gene is located on chromosome 2.

    ID gène

    8910

    UniProt

    O43556
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