Human Huntingtin Associated Protein 1 (HAP1) activation kit by CRISPRa

Specifications

Product Data
Format	3 gRNAs (5ug each), 1 scramble ctrl (10ug) and 1 enhancer vector (10ug)
Symbol	HAP1
Locus ID	9001
Kit Components	GA105986G1, Huntingtin Associated Protein 1 gRNA vector 1 in pCas-Guide-GFP-CRISPRa GA105986G2, Huntingtin Associated Protein 1 gRNA vector 2 in pCas-Guide-GFP-CRISPRa GA105986G3, Huntingtin Associated Protein 1 gRNA vector 3 in pCas-Guide-GFP-CRISPRa 1 CRISPRa-Enhancer vector, SKU GE100056 1 CRISPRa scramble vector, SKU GE100077
Reference Data
RefSeq	NM_001079870, NM_001079871, NM_003949, NM_177977, NM_001367459, NM_001367460, NM_001367461, NM_001367462
Synonyms	HAP2; hHLP1; HIP5; HLP
Summary	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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