NK2 Homeobox 5 (NKX2-5) Antibody

Por favor contáctenos para obtener información detallada sobre el precio y disponibilidad.
Description
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.
Documents del producto
Product specifications
Category | Primary Antibodies |
Immunogen Target | NK2 Homeobox 5 (NKX2-5) |
Host | Rabbit |
Reactivity | Human, Mouse, Rat |
Recommended Dilution | WB: 1/500 - 1/2000. Optimal dilutions/concentrations should be determined by the end user. |
Clonality | Polyclonal |
Conjugation | Unconjugated |
Isotype | IgG |
Purification | Purified by affinity chromatography. |
Size 1 | 60 µl |
Size 2 | 120 µl |
Size 3 | 200 µl |
Form | Liquid |
Tested Applications | WB |
Buffer | PBS, pH 7.3, containing 0.02% sodium azide, 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_004378.1 |
Background | Antibody anti-NKX2-5 |
Status | RUO |
Note | Concentration: 1 mg/ml - |
Descripción
Related Products

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
Recombinant Human NKX2-5
Ver Producto
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