NK2 Homeobox 5 (NKX2-5) Antibody

Product Graph
169€ (20 µl)

Por favor contáctenos para obtener información detallada sobre el precio y disponibilidad.

935106861
info@markelab.com
name
NK2 Homeobox 5 (NKX2-5) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx320608
tested applications
ELISA, IHC

Description

NKX2-5 Antibody is a Rabbit Polyclonal against NKX2-5.

Documents del producto

Instrucciones
Data sheet
Descargar

Product specifications

Category
Primary Antibodies
Immunogen Target
NK2 Homeobox 5 (NKX2-5)
Host
Rabbit
Reactivity
Human
Recommended Dilution
IHC: 1/20 - 1/200. Optimal dilutions/concentrations should be determined by the end user.
Clonality
Polyclonal
Conjugation
Unconjugated
Isotype
IgG
Purification
Antigen Affinity Chromatography.
Size 1
20 µl
Size 2
50 µl
Size 3
100 µl
Size 4
200 µl
Size 5
1 ml
Form
Liquid
Tested Applications
ELISA, IHC
Buffer
PBS, pH 7.3, containing 0.02% sodium azide and 50% glycerol.
Availability
Shipped within 5-10 working days.
Storage
Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
Dry Ice
No
UniProt ID
P52952
Gene ID
1482
NCBI Accession
NP_001159647.1, NM_001166175.1, NP_001159648.1, NM_001166176.1, NP_004378.1, NM_004387.3
OMIM
108900
Background
Antibody anti-NKX2-5
Status
RUO

Descripción

Related Products

FNab05751

NKX2-5 antibody

Implicated in commitment to and/or differentiation of the myocardial lineage. Acts as a transcriptional activator of ANF in cooperation with GATA4(By similarity). It is transcriptionally controlled by PBX1 and acts as a transcriptional repressor of CDKN2B(By similarity). It is required for spleen development.

Ver Producto
P8568

Recombinant Human NKX2-5

Ver Producto
abx004321

NK2 Homeobox 5 (NKX2-5) Antibody

NKX2-5 Antibody is a Rabbit Polyclonal antibody against NKX2-5. 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.

Ver Producto