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. [provided by RefSeq].
Product Information
Source: HEK293
| Purity: >95% by SDS-PAGE analysis
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Purification Method: FPLC
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Gene/Protein Information
Gene Name: KALRN
| Gene Symbol: DUET, FLJ16443, HAPIP, TRAD, duo
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Gene Name Synonyms: DUET, FLJ16443, HAPIP, TRAD, duo
| NCBI Acc#: NM_001024660
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Chromosomal Location: 3q21.1-q21.2
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