GK1 Polyclonal Antibody, 100ul Cryopreservation including point mutations

including point mutations

This protein plays a key role in skeletal homeostasis and many bone density related diseases are caused by mutations in this gene

Various capacities and specifications are available

The protein is primarily localized to membrane-associated adherens junctions and focal adhesions but is also found at the endoplasmic reticulum and nucleus

A mutation in this gene has been associate

GK1 Polyclonal Antibody, 100ul Cryopreservation including point mutationsGlycerol kinase encoded by GK belongs to the FGGY kinase family. Glycerol kinase is a key enzyme in the regulation of glycerol uptake and metabolism. It catalyzes the phosphorylation of glycerol by ATP, yielding ADP and glycerol 3 phosphate. Mutations in this gene are associated with glycerol kinase deficiency (GKD). Alternatively spliced transcript variants encoding different isoforms have been found for this gene.