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HAP1 Polyclonal Antibody, 100ul Antisense Oligonucleotides and they map to the

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HAP1 Polyclonal Antibody, 100ul Antisense Oligonucleotides and they map to theHuntington'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

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Description

and they map to the regions syntenic between mouse and human chromosomes

The first exon of this gene is unrelated to immunoglobulin variable genes

This gene encodes a member of the PRDI-BF1 and RIZ homology domain containing (PRDM) family of transcriptional regulators

NBEAL2 contains one BEACH domain and five WD repeats

HAP1 Polyclonal Antibody, 100ul Antisense Oligonucleotides and they map to theHuntington'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

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