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Description
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
Specifications
Specifications
| Antigen | LPL |
| Applications | ELISA, Western Blot |
| Classification | Monoclonal |
| Clone | 2C5 |
| Conjugate | Unconjugated |
| Description | Mouse monoclonal antibody raised against partial recombinant LPL. |
| Dilution | ELISA (1:10000) Western Blot (1:500-1:2000) The optimal working dilution should be determined by the end user. |
| Formulation | In ascites (0.03% sodium azide) |
| Gene | LPL |
| Gene Alias | HDLCQ11/LIPD |
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