LPL Monoclonal Antibody, 50ul Electronic Pipette Allelic variations in this gene

Allelic variations in this gene are associated with heparin cofactor II deficiency

this HAT can acetylate soluble but not nucleosomal histone H4 at lysines 5 and 12

as their activation can be triggered by calcium influx and oxidative stress

Consisting of 237 million bases

Mutations in this gene cause ovarian dysgenesis type 1

LPL Monoclonal Antibody, 50ul Electronic Pipette Allelic variations in this geneLPL encodes lipoprotein lipase, which is expressed in heart, muscle, and adipose tissue. LPL functions as a homodimer, and has the dual functions of triglyceride hydrolase and ligand bridging factor for receptor mediated lipoprotein uptake. Severe mutations that cause LPL deficiency result in type I hyperlipoproteinemia, while less extreme mutations in LPL are linked to many disorders of lipoprotein metabolism.