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CHRND anticorps (AA 22-245)

Cet anticorps Souris Monoclonal détecte spécifiquement CHRND dans WB, ELISA et FACS. Il présente une réactivité envers Humain.
N° du produit ABIN5611361

Aperçu rapide pour CHRND anticorps (AA 22-245) (ABIN5611361)

Antigène

Voir toutes CHRND Anticorps
CHRND (Cholinergic Receptor, Nicotinic, delta (Muscle) (CHRND))

Reactivité

  • 29
  • 7
  • 7
  • 5
  • 4
  • 4
  • 4
  • 3
  • 3
  • 2
  • 1
  • 1
Humain

Hôte

  • 28
  • 1
Souris

Clonalité

  • 28
  • 1
Monoclonal

Conjugué

  • 21
  • 2
  • 2
  • 2
  • 1
  • 1
Cet anticorp CHRND est non-conjugé

Application

  • 23
  • 15
  • 9
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Flow Cytometry (FACS)

Clone

1H1F9
  • Épitope

    • 7
    • 5
    • 4
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 22-245

    Fonction

    CHRND Antibody

    Purification

    Purified antibody

    Immunogène

    Purified recombinant fragment of human CHRND (AA: 22-245) 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

    Purified antibody in PBS with 0.05 % 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.
  • Antigène

    CHRND (Cholinergic Receptor, Nicotinic, delta (Muscle) (CHRND))

    Autre désignation

    CHRND

    Sujet

    The acetylcholine receptor of muscle has 5 subunits of 4 different types: 2 alpha and 1 each of beta, gamma and delta subunits. After acetylcholine binding, the receptor undergoes an extensive conformation change that affects all subunits and leads to opening of an ion-conducting channel across the plasma membrane. Defects in this gene are a cause of multiple pterygium syndrome lethal type (MUPSL), congenital myasthenic syndrome slow-channel type (SCCMS), and congenital myasthenic syndrome fast-channel type (FCCMS). Several transcript variants encoding different isoforms have been found for this gene.

    Poids moléculaire

    58.8 kDa

    ID gène

    1144

    UniProt

    Q07001
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