AHI1 antibody [N1], N-term

GeneTex

AHI1 antibody [N1], N-term

9

Research Use Only

1 mg/ml

IgG

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. [provided by RefSeq]

2°C to 8°C,-20°C

12352203