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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. [provided by RefSeq].
Titration of the LPL antibody may be required due to differences in protocols and secondary/substrate sensitivity.
A portion of amino acids 300-327 from the human protein was used as the immunogen for this LPL antibody.
Aliquot the LPL antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.
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