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Actin anticorps

Cet anticorps anti-Actin est un anticorps Lapin Polyclonal détectant Actin dans WB et ELISA. Adapté pour Humain, Souris et Rat.
N° du produit ABIN7000360

Aperçu rapide pour Actin anticorps (ABIN7000360)

Antigène

Voir toutes Actin (ACTA1) Anticorps
Actin (ACTA1) (Actin, alpha 1, Skeletal Muscle (ACTA1))

Reactivité

  • 88
  • 45
  • 39
  • 15
  • 10
  • 9
  • 9
  • 7
  • 6
  • 5
  • 5
  • 5
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Humain, Souris, Rat

Hôte

  • 76
  • 31
Lapin

Clonalité

  • 72
  • 32
  • 1
Polyclonal

Conjugué

  • 61
  • 12
  • 11
  • 10
  • 4
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp Actin est non-conjugé

Application

  • 83
  • 59
  • 44
  • 25
  • 24
  • 20
  • 10
  • 9
  • 6
  • 2
  • 1
  • 1
Western Blotting (WB), ELISA
  • Attributs du produit

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogène

    Recombinant protein of human ACTA1

    Isotype

    IgG
  • Indications d'application

    WB 1:200-1:1000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.2 mg/mL

    Buffer

    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4

    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

    Actin (ACTA1) (Actin, alpha 1, Skeletal Muscle (ACTA1))

    Autre désignation

    ACTA1

    Sujet

    The product encoded by this gene belongs to the actin family of proteins, which are highly conserved proteins that play a role in cell motility, structure and integrity. Alpha, beta and gamma actin isoforms have been identified, with alpha actins being a major constituent of the contractile apparatus, while beta and gamma actins are involved in the regulation of cell motility. This actin is an alpha actin that is found in skeletal muscle. Mutations in this gene cause nemaline myopathy type 3, congenital myopathy with excess of thin myofilaments, congenital myopathy with cores, and congenital myopathy with fiber-type disproportion, diseases that lead to muscle fiber defects.

    Poids moléculaire

    42 kDa

    UniProt

    P68133

    Pathways

    Caspase Cascade in Apoptosis, Myometrial Relaxation and Contraction, Skeletal Muscle Fiber Development
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