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021-54845833/15800441009
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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. |
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Applications: |
ELISA, IHC |
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Name of antibody: |
LPL |
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Immunogen: |
Synthetic peptide of human LPL |
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Full name: |
lipoprotein lipase |
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Synonyms: |
LIPD; HDLCQ11 |
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SwissProt: |
P06858 |
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ELISA Recommended dilution: |
5000-10000 |
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IHC positive control: |
Human tonsil |
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IHC Recommend dilution: |
25-100 |
