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MYOZ2 anticorps

Cet anticorps anti-MYOZ2 est un anticorps Lapin Polyclonal détectant MYOZ2 dans WB et ELISA. Adapté pour Humain et Souris.
N° du produit ABIN7252480

Aperçu rapide pour MYOZ2 anticorps (ABIN7252480)

Antigène

Voir toutes MYOZ2 Anticorps
MYOZ2 (Myozenin 2 (MYOZ2))

Reactivité

  • 32
  • 6
  • 3
  • 1
Humain, Souris

Hôte

  • 29
  • 4
Lapin

Clonalité

  • 30
  • 3
Polyclonal

Conjugué

  • 19
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp MYOZ2 est non-conjugé

Application

  • 22
  • 16
  • 5
  • 4
  • 2
  • 2
  • 1
Western Blotting (WB), ELISA
  • Attributs du produit

    Polyclonal Antibody

    Purification

    Antigen affinity purification

    Immunogène

    Full length fusion protein

    Isotype

    IgG
  • Indications d'application

    WB 1:500-1:2000, ELISA 1:5000-1:10000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1.08 mg/mL

    Buffer

    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

    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

    -20 °C

    Stockage commentaire

    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène

    MYOZ2 (Myozenin 2 (MYOZ2))

    Autre désignation

    MYOZ2

    Sujet

    MYOZ2 (Myozenin 2) is a Protein Coding gene. Diseases associated with MYOZ2 include Cardiomyopathy, Hypertrophic, 16 and Myoz2-Related Familial Hypertrophic Cardiomyopathy. GO annotations related to this gene include actin binding and telethonin binding. An important paralog of this gene is MYOZ1.The protein encoded by this gene belongs to a family of sarcomeric proteins that bind to calcineurin, a phosphatase involved in calcium-dependent signal transduction in diverse cell types. These family members tether calcineurin to alpha-actinin at the z-line of the sarcomere of cardiac and skeletal muscle cells, and thus they are important for calcineurin signaling. Mutations in this gene cause cardiomyopathy familial hypertrophic type 16, a hereditary heart disorder.

    Poids moléculaire

    Observed_MW: Refer to figures

    Calculated_MW: 30 kDa

    UniProt

    Q9NPC6
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