LPL encodes lipoprotein lipase, which is expressed innheart, muscle, and adipose tissue. LPL functions as a homodimer,nand has the dual functions of triglyceride hydrolase andnligand/bridging factor for receptor-mediated lipoprotein uptake.nSevere mutations that cause LPL deficiency result in type Inhyperlipoproteinemia, while less extreme mutations in LPL arenlinked to many disorders of lipoprotein metabolism. [provided bynRefSeq].
应用类型
WB,FCM
免疫原
This LPL antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 300-327 amino acids from the Central region of human LPL.
