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AHI1 Rabbit anti-Human, Mouse, Polyclonal, Proteintech
Rabbit Polyclonal Antibody
Marque: Proteintech 22045-1-AP-20UL
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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.Spécification
| AHI1 | |
| Polyclonal | |
| Unconjugated | |
| AHI1 | |
| AHI 1, AHI1, JBTS3, Jouberin, ORF1 | |
| Rabbit | |
| Antigen Affinity Chromatography | |
| RUO | |
| 52906, 54806 | |
| -20°C | |
| Liquid |
| Western Blot | |
| 0.18 mg/mL | |
| PBS with 50% glycerol and 0.02% sodium azide; pH 7.3 | |
| Q8K3E5, Q8N157 | |
| Ahi1 | |
| AHI1 Fusion Protein Ag16885 | |
| 20 μL | |
| Primary | |
| Human, Mouse | |
| Antibody | |
| IgG |
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