SGLT-1 Polyclonal Antibody, 20ul DNA Fragments Genetic variation in this gene

Genetic variation in this gene is associated with diabetes mellitus insulin-dependent type 19

whereupon it binds to the growth hormone secretagogue receptor in the hypothalamus which results in the secretion of growth hormone (somatotropin)

Mixed lineage kinase domain-like protein plays a critical role in tumor necrosis factor (TNF)-induced necroptosis

This protein localizes to the endoplasmic reticulum

CHSY1 encodes a member of the chondroitin N-acetylgalactosaminyltransferase family

SGLT-1 Polyclonal Antibody, 20ul DNA Fragments Genetic variation in this geneSLC5A1 (solute carrier family 5 member 1) encodes a member of the sodium dependent glucose transporter (SGLT) family. The encoded integral membrane protein is the primary mediator of dietary glucose and galactose uptake from the intestinal lumen. Mutations in SLC5A1 have been associated with glucose galactose malabsorption. Multiple transcript variants encoding different isoforms have been found for SLC5A1.