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, Jul 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| LPLBA-20-REGO | 20 (40 μL) | 200 μL |
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| LPLBA-20-REGR | 20 (40 μL) | 200 μL |
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| LPLBA-20-ORGR | 20 (40 μL) | 200 μL |
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| LPLBA-20-GOGR | 20 (40 μL) | 200 μL |
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| LPLBA-20-GRRE | 20 (40 μL) | 200 μL |
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| LPLBA-20-GROR | 20 (40 μL) | 200 μL |
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| LPLBA-20-GRGO | 20 (40 μL) | 200 μL |
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| LPLBA-20-AQOR | 20 (40 μL) | 200 μL |
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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, Jul 2008]
Gene Symbol : LPL
Gene Name : Lipoprotein lipase
Chromosome : CHR 8: 199,390,70-199,672,58
Locus : 8p21.3
Alt. Genes : FEM1B
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