NK2 Homeobox 5 anticorps (AA 82-111)

N° du produit ABIN1538648

L’anticorps anti-NK2 Homeobox 5 Polyclonal Lapin est utilisé pour la détection de NK2 Homeobox 5 dans des échantillons de Humain et Souris. Il a été validé pour WB.

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

Antigène: NK2 Homeobox 5 (NKX2-5)

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp NK2 Homeobox 5 est non-conjugé

Application: Western Blotting (WB)

Clone: RB36777

Détail du produit anti-NK2 Homeobox 5 anticorps

Épitope: 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

Information d'application

Indications d'application: WB: 1:2000

Restrictions: For Research Use only

Stockage

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

Détails sur NK2 Homeobox 5

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