NKX2-5 antibody (clone S1), anti-human
€435.00
In stock
SKU
AC-AT3057a
Catalog Number: AC-AT3057a
Size: 100 µg
Isotype: mouse IgG1 Kappa
Applications: WB, E
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Size: 100 µg
Isotype: mouse IgG1 Kappa
Applications: WB, E
Request Information AC-AT3057a">Request Information
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.
Other Names:
Homeobox protein Nkx-25, Cardiac-specific homeobox, Homeobox protein CSX, Homeobox protein NK-2 homolog E, NKX2-5, CSX, NKX25, NKX2E
Antigen Type:
Recombinant Protein
Gene Name: NKX2-5
Gene ID: 1482
NCBI Accession: NP_001159647.1;NP_001159648.1;NP_004378.1
Primary Accession: P52952
Other Accession: BC025711
Format: Clear, colorless solution in phosphate buffered saline, pH 7.2 .
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.
Other Names:
Homeobox protein Nkx-25, Cardiac-specific homeobox, Homeobox protein CSX, Homeobox protein NK-2 homolog E, NKX2-5, CSX, NKX25, NKX2E
Antigen Type:
Recombinant Protein
Gene Name: NKX2-5
Gene ID: 1482
NCBI Accession: NP_001159647.1;NP_001159648.1;NP_004378.1
Primary Accession: P52952
Other Accession: BC025711
Format: Clear, colorless solution in phosphate buffered saline, pH 7.2 .
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