Home Antibody All anti-HAP1 antibodies
Also for HAP1 (NM_001079870)
|HAP1 antibody was raised against a 19 amino acid peptide from near the center of human HAP1.|
|Human, Mouse, Rat
||Lot dependent; please refer to CoA along with shipment
||WB: 0.5 - 1 ug/ml
|PBS containing 0.02% sodium azide.|
|Affinity chromatography purified via peptide column
|Homo sapiens huntingtin-associated protein 1 (HAP1), transcript variant 3|
|HAP2; hHLP1; HIP5; HLP|
Entrez Gene 9001 Human
Entrez Gene 15114 Mouse
Entrez Gene 29430 Rat
|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. HAP1 was initially identified through a two-hybrid library screening; the binding of HAP1 to huntingtin correlated with the expansion of the polyglutamine tract. HAP1 also interacts with two cytoskeletal proteins (dynactin and pericentriolar autoantigen protein 1), suggesting that HAP1 may play a role in vesicular trafficking or organelle transport. HAP1 is also involved with the huntingtin-enhanced BDNF transport along the cellular microtubles. Attenuation of this process led to the loss of neurotrophic support and neuronal toxicity, which suggests that loss of this function might contribute to pathogenesis. Several alternatively spliced isoforms have been described for HAP1.|
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Western blot analysis of HAP1 in mouse brain tissue lysate with HAP1 antibody at (A) 0.5 and (B) 1 ug/ml.
Immunohistochemistry of HAP1 in human brain tissue with HAP1 antibody at 2.5 ug/ml.