LPL: lipoprotein lipase, also known as LIPD, HDLCQ11. Entrez Protein: NP_000228. It 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.

Aliases ：   LIPD, HDLCQ11    

Entrez GeneID：    4023    

Swissprot ：   P06858    

WB Predicted band size：    53.1kDa    

Host/Isotype  ：  Mouse IgG1    

Species Reactivity ：   Human    

Immunogen  ：  Purified recombinant fragment of LPL expressed in E. Coli.    

WB    1/500 - 1/2000    

ELISA    1/10000