Synthetic peptide sequence: 103-132aa, AKDPRAEKKELCALQKAVELEKTEADNAER.
Reconstitution information: Add 0.2 mL of distilled water will yield a concentration of 500 µg/mL.
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.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: Cardiac-specific homeobox; cardiac-specific homeobox 1; CSX, NKX2.5, NKX2E; Drosophila NK2 transcription factor related, locus 5; Homeobox protein CSX; Homeobox protein NK-2 homolog E; homeobox protein NKX 2-5; Homeobox protein Nkx-2.5; NK2 transcription factor related locus 5; NK2 transcription factor related, locus 5; NKX 2-5; NKX2-5; tinman paralog
Gene Aliases: CHNG5; CSX; CSX1; HLHS2; Nkx-2.5; NKX2-5; NKX2.5; NKX2E; NKX4-1; tinman; VSD3