Recombinant fusion protein of human AHI1(NP_001128304.1).
Conjugation:
Unconjugated
Alternative Names:
AHI1,AHI-1,JBTS3,ORF1,dJ71N10.1,jouberin
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.
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE).
Form:
1mg/ml in PBS with 0.02% sodium azide, 50% glycerol, pH7.2
Application Dilute:
IHC,1:50 - 1:200
Application Notes:
Unmodification
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