兔抗AHI1多克隆抗體

Background:

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.

Applications:

ELISA, IHC

Name of antibody:

AHI1

Immunogen:

Synthetic peptide of humanAHI1

Full name:

Abelson helper integration site 1

Synonyms：

ORF1; AHI-1; JBTS3; dJ71N10.1

SwissProt:

Q8N157

ELISA Recommended dilution:

2000-5000

IHC positive control:

Human liver cancer

IHC Recommend dilution:

25-100