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AHI1 Antibody

Abelson helper integration site 1 (AHI1) is also known as jouberin. AHI1 is apparently required for both cerebellar and cortical development in humans. Mutations in AH1 cause specific forms of Joubert syndrome-related disorders. Joubert syndrome (JS) is a recessively inherited developmental brain disorder with several identified causative chromosomal loci [taken from NCBI Entrez Gene (Gene ID: 55054)].
AHI1
Abelson helper integration site 1
Jouberin
:  abelson helper integration site 1 protein homolog AHI-1 contatins SH3 and WD40 domains dJ71N10.1 JBTS3 jouberin ORF1
Product
Specifications
Ordering Information
Human
IP
between 25 and 75
$339
$99
Human
WB, IP
between 1146 and 1196
$339
$229
$99
Human
WB, IP
Includes: 1 each of A303-300A and A303-301A
$472