Full Product Name
AHI1 Antibody, HRP Conjugated
Product Synonym Names
Jouberin; Abelson helper integration site 1 protein homolog; AHI-1; AHI1
Product Gene Name
anti-AHI1 antibody
[Similar Products]
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
3D Structure
ModBase 3D Structure for Q8N157
Purity/Purification
>95%
Protein G Purified
Immunogen
Recombinant Human Jouberin protein (1-213AA)
Preservative
0.03% Proclin 300
Constituents
50% Glycerol, 0.01M PBS, pH 7.4
Preparation and Storage
Upon receipt, store at-20 degree C or-80 degree C. Avoid repeated freeze.
ISO Certification
Manufactured in an ISO 13485:2003 and EN ISO 13485:2012 Certified Laboratory.
Other Notes
Small volumes of anti-AHI1 antibody vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
Product Categories/Family for anti-AHI1 antibody
Cell Biology
Applications Tested/Suitable for anti-AHI1 antibody
ELISA (EIA)
NCBI/Uniprot data below describe general gene information for AHI1. It may not necessarily be applicable to this product.
NCBI Accession #
NP_001128302.1
[Other Products]
NCBI GenBank Nucleotide #
NM_001134830.1
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UniProt Primary Accession #
Q8N157
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UniProt Secondary Accession #
Q4FD35; Q504T3; Q5TCP9; Q6P098; Q6PIT6; Q8NDX0; Q9H0H2; E1P584[Other Products]
UniProt Related Accession #
Q8N157[Other Products]
Molecular Weight
120,853 Da
NCBI Official Full Name
jouberin isoform a
NCBI Official Synonym Full Names
Abelson helper integration site 1
NCBI Official Symbol
AHI1 [Similar Products]
NCBI Official Synonym Symbols
ORF1; AHI-1; JBTS3; dJ71N10.1
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NCBI Protein Information
jouberin
UniProt Protein Name
Jouberin
UniProt Synonym Protein Names
Abelson helper integration site 1 protein homolog; AHI-1
UniProt Gene Name
AHI1 [Similar Products]
UniProt Synonym Gene Names
AHI-1 [Similar Products]
NCBI Summary for AHI1
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, Oct 2008]
UniProt Comments for AHI1
Involved in vesicle trafficking and required for ciliogenesis, formation of primary non-motile cilium, and recruitment of RAB8A to the basal body of primary cilium. Component of the tectonic-like complex, a complex localized at the transition zone of primary cilia and acting as a barrier that prevents diffusion of transmembrane proteins between the cilia and plasma membranes. Involved in neuronal differentiation. As a positive modulator of classical Wnt signaling, may play a crucial role in ciliary signaling during cerebellum embryonic development (PubMed:21623382).
Research Articles on AHI1
1. Two copies of the MS risk allele within AHI1 (rs11154801) is associated with increased relapses among children and *****s.
Precautions
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Disclaimer
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