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NK2 Homeobox 5 anticorps (AA 2-5)

Cet anticorps Lapin Polyclonal détecte spécifiquement NK2 Homeobox 5 dans WB et ELISA. Il présente une réactivité envers Humain et Souris.
N° du produit ABIN3032008

Aperçu rapide pour NK2 Homeobox 5 anticorps (AA 2-5) (ABIN3032008)

Antigène

Voir toutes NK2 Homeobox 5 (NKX2-5) Anticorps
NK2 Homeobox 5 (NKX2-5)

Reactivité

  • 41
  • 19
  • 7
  • 5
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Humain, Souris

Hôte

  • 42
  • 8
  • 1
Lapin

Clonalité

  • 44
  • 7
Polyclonal

Conjugué

  • 41
  • 3
  • 2
  • 2
  • 2
  • 1
Cet anticorp NK2 Homeobox 5 est non-conjugé

Application

  • 43
  • 28
  • 8
  • 6
  • 6
  • 4
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB), ELISA
  • Épitope

    • 7
    • 5
    • 4
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 2-5

    Purification

    Antigen affinity purified

    Immunogène

    A portion of amino acids 2-5 from the human protein was used as the immunogen for this NKX2.5 antibody.

    Isotype

    Ig Fraction
  • Indications d'application

    Titration of the NKX2.5 antibody may be required due to differences in protocols and secondary/substrate sensitivity.\. Western blot: 1:1000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    In 1X PBS, pH 7.4, with 0.09 % 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

    -20 °C

    Stockage commentaire

    Aliquot the NKX2.5 antibody and store frozen at -20°C or colder. Avoid repeated freeze-thaw cycles.
  • Antigène

    NK2 Homeobox 5 (NKX2-5)

    Autre désignation

    NKX2.5

    Sujet

    This gene encodes a homeobox-containing transcription factor. This transcription factor functions in heart formation and development. Mutations in this gene cause atrial septal defect with atrioventricular conduction defect, and also tetralogy of Fallot, which are both heart malformation diseases. Mutations in this gene can also cause congenital hypothyroidism non-goitrous type 5, a non-autoimmune condition. Alternative splicing results in multiple transcript variants.

    UniProt

    P52952

    Pathways

    Regulation of Muscle Cell Differentiation, Skeletal Muscle Fiber Development
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