HAP1 蛋白
(Huntingtin Associated Protein 1 (HAP1))
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 huntingtin, with two cytoskeletal proteins (dynactin and pericentriolar autoantigen protein 1), and with a hepatocyte growth factor-regulated tyrosine kinase substrate. The interactions with cytoskeletal proteins and a kinase substrate suggest a role for this protein in vesicular trafficking or organelle transport. Several alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2008].
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8 results
HAP1
宿主: 人
宿主: 大肠杆菌（E. Coli）
Recombinant
>95 %
SDS, WB, Imm, PC
HAP1
宿主: 小鼠
宿主: 大肠杆菌（E. Coli）
Recombinant
> 95 %
SDS, WB, Imm, PC
HAP1
宿主: 大鼠
宿主: 大肠杆菌（E. Coli）
Recombinant
> 90 %
SDS, WB, Imm, PC
custom-made
HAP1
宿主: 小鼠
宿主: Cell-free protein synthesis (CFPS)
Recombinant
approximately 70-80 % as determined by SDS PAGE, Western Blot and analytical SEC (HPLC).
SDS, WB, ELISA
custom-made
HAP1
宿主: 人
宿主: Cell-free protein synthesis (CFPS)
Recombinant
approximately 70-80 % as determined by SDS PAGE, Western Blot and analytical SEC (HPLC).
SDS, WB, ELISA
Aliases for HAP1 蛋白
huntingtin associated protein 1 (HAP1) 蛋白huntingtin-associated protein 1 (Hap1) 蛋白
HAP-1 蛋白
HAP1-A 蛋白
HAP1-B 蛋白
HAP2 蛋白
hHLP1 蛋白
HIP5 蛋白
HLP 蛋白
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