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NK2 Homeobox 5 anticorps (AA 82-111)

L’anticorps Lapin Polyclonal anti-NK2 Homeobox 5 a été validé pour WB. Il convient pour détecter NK2 Homeobox 5 dans des échantillons de Humain et Souris.
N° du produit ABIN1538648

Aperçu rapide pour NK2 Homeobox 5 anticorps (AA 82-111) (ABIN1538648)

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
  • 29
  • 8
  • 6
  • 6
  • 4
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB)

Clone

RB36777
  • Épitope

    • 6
    • 5
    • 4
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 82-111

    Purification

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogène

    This NKX2-5 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 82-111 amino acids from the Central region of human NKX2-5.

    Isotype

    Ig Fraction
  • Indications d'application

    WB: 1:2000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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

    NKX2-5 Antibody (Center) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

    Date de péremption

    6 months
  • 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.

    Poids moléculaire

    34918

    ID gène

    1482

    NCBI Accession

    NP_001159647, NP_001159648, NP_004378

    UniProt

    P52952

    Pathways

    Regulation of Muscle Cell Differentiation, Skeletal Muscle Fiber Development
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