兔抗LPL多克隆抗体

Background:

LPL 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.

Applications:

ELISA, IHC

Name of antibody:

LPL

Immunogen:

Synthetic peptide of human LPL

Full name:

lipoprotein lipase

Synonyms:

LIPD; HDLCQ11

SwissProt:

P06858

ELISA Recommended dilution:

5000-10000

IHC positive control:

Human tonsil

IHC Recommend dilution:

25-100