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Predicted molecular weight: 53 kDa.
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.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: adipose lipoprotein lipase; alpha lipase; lipopotein lipase precursor; Lipoprotein lipase; lipoprotein lipase (EC 3.1.1.34); LPL; O 1-4-5; Phospholipase A1; triacylglycerol lipase
基因别名: HDLCQ11; LIPD; LPL
UniProt ID: (Chicken) P11602, (Human) P06858, (Bovine) P11151, (Rat) Q06000, (Guinea pig) P11153, (Mouse) P11152
Entrez Gene ID: (Chicken) 396219, (Human) 4023, (Bovine) 280843, (Rat) 24539, (Guinea pig) 100135570, (Mouse) 16956