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AHI1 Rabbit anti-Human, Polyclonal, Bethyl Laboratories
Rabbit Polyclonal Antibody
Supplier: Bethyl Laboratories, Inc A303300AT

Description
The recommended shelf life for this product is 1 year from date of receipt.
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.Specifications
AHI1 | |
Polyclonal | |
Unconjugated | |
AHI1 | |
RP1-32B1.2, AHI-1, JBTS3, ORF1, dJ71N10.1, abelson helper integration site 1 protein homolog, contatins SH3 and WD40 domains, jouberin | |
Rabbit | |
Antigen affinity chromatography | |
RUO | |
54806 | |
4° C | |
Liquid |
Immunoprecipitation | |
1 mg/ml | |
phosphate, tris citrate with 0.09% sodium azide; pH 7-8 | |
Q8N157 | |
AHI1 | |
Between 25 and 75 | |
10 μL | |
Primary | |
Human | |
Antibody | |
IgG |
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