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Nkx-2.5 Monoclonal Antibody

Monoclonal antibody

Specification

BYab-15733

  • 50UL $180 100UL $255
  • Delivery: In Stock

Product introduction Experimental scheme Citation Related products

Product introduction>

Host
Reactiveness
Use
Molecular weight (DA)
Immunogen
Purified recombinant fragment of human Nkx-2.5 expressed in E. Coli.
Specificity
Nkx-2.5 Monoclonal Antibody detects endogenous levels of Nkx-2.5 protein.
Source
Monoclonal, Mouse
Formulation
Antibody are purified by protein G affinity chromatography. Liquid in PBS containing 0.03% sodium azide.
Dilution rate
Western Blot: 1/500 - 1/2000. ELISA: 1/10000. Not yet tested in other applications.
Purification process (Immunogen)
Affinity purification
Concentration
1 mg/ml
Background
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. [provided by RefSeq, Oct 2009],
Function
disease:Defects in NKX2-5 are a cause of tetralogy of Fallot (TOF) [MIM:187500]. TOF is a congenital heart anomaly which consists of pulmonary stenosis, ventricular septal defect, dextroposition of the aorta (aorta is on the right side instead of the left) and hypertrophy of the right ventricle. This condition results in a blue baby at birth due to inadequate oxygenation. Surgical correction is emergent.,disease:Defects in NKX2-5 are the cause of atrial septal defect with atrioventricular conduction defects (ASD-AVCD) [MIM:108900]. ASD-AVCD is a congenital heart malformation characterized by atrioventricular conduction defects and incomplete closure of the wall between the atria resulting in blood flow from the left to the right atria.,disease:Defects in NKX2-5 are the cause of congenital hypothyroidism non-goitrous type 5 (CHNG5) [MIM:225250]. CHNG5 is a non-autoimmune condition charact
Gene Name
NKX2-5
Protein name
Homeobox protein Nkx-2.5
Abbreviation
Nkx-2.5
Other name
NKX2-5; CSX; NKX2.5; NKX2E; Homeobox protein Nkx-2.5; Cardiac-specific homeobox; Homeobox protein CSX; Homeobox protein NK-2 homolog E
Fields
Human gene ID
1482
Human protein sequence Database
P52952
Mouse gene ID
Mouse protein sequence database
P42582
Rat gene ID
Rat protein sequence database
Cellular localization
Nucleus .
Tissue expression
Expressed only in the heart.
Storage
-20°C/1 year

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Nkx-2.5 Monoclonal Antibody

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