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HAP1 Polyclonal Antibody, 100ul Antisense Oligonucleotides The first exon of this

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HAP1 Polyclonal Antibody, 100ul Antisense Oligonucleotides The first exon of thisHuntington'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

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

RXFP3 (Relaxin/Insulin Like Family Peptide Receptor 3) is a Protein Coding gene

and calmodulin

Proteins belonging to this family play a central role in inducible gene transcription during the immune response

HAP1 Polyclonal Antibody, 100ul Antisense Oligonucleotides The first exon of thisHuntington'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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