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NKX2-5 Rabbit anti-Human, Polyclonal, Proteintech

Rabbit Polyclonal Antibody
Supplier: Proteintech Group Inc 139211AP150UL
Description
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.Specifications
| NKX2-5 | |
| Polyclonal | |
| Unconjugated | |
| NKX2-5 | |
| Cardiac specific homeobox, CHNG5, CSX, CSX1, Homeobox protein CSX, Homeobox protein Nkx 2.5, NKX2 5, NKX2.5, NKX2-5, NKX2E, NKX4 1 | |
| Rabbit | |
| Antigen Affinity Chromatography | |
| RUO | |
| 1482 | |
| -20°C | |
| Liquid |
| Immunohistochemistry (Paraffin), Western Blot | |
| 0.13 mg/mL | |
| PBS with 50% glycerol and 0.02% sodium azide; pH 7.3 | |
| P52952 | |
| NKX2-5 | |
| NKX2-5 Fusion Protein Ag4930 | |
| 150 μL | |
| Primary | |
| Human | |
| Antibody | |
| IgG |
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