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TNNT1 anticorps

L’anticorps Lapin Polyclonal anti-TNNT1 a été validé pour WB, IHC et ELISA. Il convient pour détecter TNNT1 dans des échantillons de Humain et Souris.
N° du produit ABIN7254007

Aperçu rapide pour TNNT1 anticorps (ABIN7254007)

Antigène

Voir toutes TNNT1 Anticorps
TNNT1 (Slow Skeletal Troponin T (TNNT1))

Reactivité

  • 19
  • 8
  • 6
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Humain, Souris

Hôte

  • 18
  • 6
  • 1
Lapin

Clonalité

  • 21
  • 4
Polyclonal

Conjugué

  • 20
  • 3
  • 2
Cet anticorp TNNT1 est non-conjugé

Application

  • 25
  • 13
  • 9
  • 8
  • 4
  • 3
  • 3
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), ELISA
  • Attributs du produit

    Polyclonal Antibody

    Purification

    Antigen affinity purification

    Immunogène

    Fusion protein of human TNNT1

    Isotype

    IgG
  • Indications d'application

    WB 1:500-1:2000, IHC 1:25-1:50, ELISA 1:5000-1:10000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.66 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

    TNNT1 (Slow Skeletal Troponin T (TNNT1))

    Autre désignation

    TNNT1

    Sujet

    This gene encodes a protein that is a subunit of troponin, which is a regulatory complex located on the thin filament of the sarcomere. This complex regulates striated muscle contraction in response to fluctuations in intracellular calcium concentration. This complex is composed of three subunits: troponin C, which binds calcium, troponin T, which binds tropomyosin, and troponin I, which is an inhibitory subunit. This protein is the slow skeletal troponin T subunit. Mutations in this gene cause nemaline myopathy type 5, also known as Amish nemaline myopathy, a neuromuscular disorder characterized by muscle weakness and rod-shaped, or nemaline, inclusions in skeletal muscle fibers which affects infants, resulting in death due to respiratory insufficiency, usually in the second year. Multiple transcript variants encoding different isoforms have been found for this gene.

    Poids moléculaire

    Observed_MW: Refer to figures

    Calculated_MW: 33 kDa

    UniProt

    P13805
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