LPL FISH Probe

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 Details
SKU Test Kits Buffer Dye Color Order Now
LPL-20-RE 20 (40 μL) 200 μL color Request Pricing
LPL-20-OR 20 (40 μL) 200 μL color Request Pricing
LPL-20-GO 20 (40 μL) 200 μL color Request Pricing
LPL-20-GR 20 (40 μL) 200 μL color Request Pricing
LPL-20-AQ 20 (40 μL) 200 μL color Request Pricing

Gene Summary

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 Details

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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