Arrdc1 Polyclonal Antibody, 50ul Culture Plate Inserts Choline transporter

Choline transporter

RLN2 and RLN3

members of which are transcription factors characterized by a ligand-binding domain and a DNA-binding domain

Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene

This gene encodes a fusion protein consisting of ubiquitin at the N terminus and ribosomal protein L40 at the C terminus

Arrdc1 Polyclonal Antibody, 50ul Culture Plate Inserts Choline transporterARRDC1, ARRDC2 (which exists as multiple alternatively spliced isoforms), ARRDC4 and ARRDC5 are arrestin domain containing proteins that are encoded by genes which map to human chromosomes 9, 15 and 19. Chromosome 9, on which the ARRDC1 gene is localized, contains 145 million base pairs and comprises 4% of the human genome, encoding nearly 900 genes. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, and