NK2 Homeobox 5 anticorps (AA 82-111)

N° du produit ABIN1538648

Détail du produit anti-NK2 Homeobox 5 anticorps

Antigène: NK2 Homeobox 5 (NKX2-5)

Épitope: AA 82-111

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp NK2 Homeobox 5 est non-conjugé

Application: Western Blotting (WB)

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.

Clone: RB36777

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 (NKX2-5 Produits)

Synonymes: anticorps CHNG5, anticorps CSX, anticorps CSX1, anticorps HLHS2, anticorps NKX2.5, anticorps NKX2E, anticorps NKX4-1, anticorps VSD3, anticorps Csx, anticorps Nkx-2.5, anticorps Nkx2.5, anticorps tinman, anticorps nk2.5, anticorps nkx2-5, anticorps zgc:111912, anticorps AR2, anticorps XNkx2-5, anticorps csx, anticorps nkx-2.5, anticorps nkx2-5b, anticorps nkx2.5, anticorps NKX2-5, anticorps Nkx2-5, anticorps csx1, anticorps nkx2e, anticorps XNkx-2.5, anticorps CNKX-2.5, anticorps NKX-2.5, anticorps NK2 homeobox 5, anticorps NK2 homeobox 5 S homeolog, anticorps NKX2-5, anticorps Nkx2-5, anticorps nkx2.5, anticorps nkx2-5.S, anticorps 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