NKX2-5 Antibody (Center) Blocking Peptide
€363.00
In stock
SKU
AC-BP17406c
Background:
This gene encodes a homeobox-containing transcriptionfactor. This transcription factor functions in heart formation anddevelopment. Mutations in this gene cause atrial septal defect withatrioventricular conduction defect, and also tetralogy of Fallot,which are both heart malformation diseases. Mutations in this genecan also cause congenital hypothyroidism non-goitrous type 5, anon-autoimmune condition. Alternative splicing results in multipletranscript variants.
Other Names:
Homeobox protein Nkx-25, Cardiac-specific homeobox, Homeobox protein CSX, Homeobox protein NK-2 homolog E, NKX2-5, CSX, NKX25, NKX2E
Gene Name: NKX2-5
Gene ID: 1482
Primary Accession: P52952
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
This gene encodes a homeobox-containing transcriptionfactor. This transcription factor functions in heart formation anddevelopment. Mutations in this gene cause atrial septal defect withatrioventricular conduction defect, and also tetralogy of Fallot,which are both heart malformation diseases. Mutations in this genecan also cause congenital hypothyroidism non-goitrous type 5, anon-autoimmune condition. Alternative splicing results in multipletranscript variants.
Other Names:
Homeobox protein Nkx-25, Cardiac-specific homeobox, Homeobox protein CSX, Homeobox protein NK-2 homolog E, NKX2-5, CSX, NKX25, NKX2E
Gene Name: NKX2-5
Gene ID: 1482
Primary Accession: P52952
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
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