Kalirin (isoform 2) polyclonal, anti-human, mouse, rat

Background:
Huntington's disease (HD), a neurodegenerative disorder characterized by loss of striatal neurons, is caused by an expansion of a polyglutamine tract in the HD protein huntingtin. This gene encodes a protein that interacts with the huntingtin-associated protein 1, which is a huntingtin binding protein that may function in vesicle trafficking. Alternatively spliced transcript variants encoding different isoforms have been described.

Other Names:
Kalirin, 2.7.11.1, Huntingtin-associated protein-interacting protein, Protein Duo, Serine/threonine-protein kinase with Dbl- and pleckstrin homology domain, KALRN, DUET, DUO, HAPIP, TRAD

Antigen Types:
Synthetic Peptide

Gene Name:
KALRN (HGNC:4814)
Gene ID:
8997
Primary Accession: O60229
Other Accession: NP_003938;8997;545156 (mouse); 84009 (rat);