This is an aptamer development services to screening aptamers binds to the AHI1 with an affinity of 1nM~1μM.
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| Target Category | Protein |
| Target | AHI1 |
| Alternative Names | Abelson Helper Integration Site 1; Jouberin; Abelson Helper Integration Site 1 Protein Homolog; AHI-1; JBTS3; ORF1; Abelson Helper Integration Site; Contatins SH3 And WD40 Domains; DJ71N10.1; FLJ20069; AHI1 |
| Gene ID | 54806 |
| UniProt ID | Q8N157 |
| Target Overview | 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. |
| Chemical Modification | N/A |
| Type | DNA |
| Length | 20-80 nt |
| Affinity (Kd) | 1nM~1μM |
| Binding Conditions/Buffer | PBS; buffer system with Serum; other |