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ROD1 Rabbit anti-Human, Mouse, Rat, Polyclonal, Proteintech

Rabbit Polyclonal Antibody
Supplier: Proteintech Group Inc 140271AP150UL
Description
This gene is apparently required for both cerebellar and cortical development in humans. This gene mutations cause specific forms of Joubert syndrome-related disorders. Joubert syndrome (JS) is a recessively inherited developmental brain disorder with several identified causative chromosomal loci. Alternatively spliced transcript variants encoding different isoforms have been identified.Specifications
| ROD1 | |
| Polyclonal | |
| Unconjugated | |
| PTBP3 | |
| PTBP3, Regulator of differentiation 1, ROD1 | |
| Rabbit | |
| Antigen Affinity Chromatography | |
| RUO | |
| 230257, 83515, 9991 | |
| -20°C | |
| Liquid |
| Immunohistochemistry (Paraffin), Western Blot | |
| 0.13 mg/mL | |
| PBS with 50% glycerol and 0.02% sodium azide; pH 7.3 | |
| O95758, Q8BHD7, Q9Z118 | |
| Ptbp3 | |
| ROD1 Fusion Protein Ag5172 | |
| 150 μL | |
| Primary | |
| Human, Mouse, Rat | |
| Antibody | |
| IgG |
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