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- Tel: 858.663.9055
- Email: info@nsjbio.com
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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. [RefSeq]
Optimal dilution of the LPL antibody should be determined by the researcher.
A synthetic peptide specific to human Lipoprotein lipase / LPL was used as the immunogen for the LPL antibody.
Store the LPL antibody at -20oC.
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