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This antibody detects human Lipoprotein Lipase/LPL in direct ELISAs and less than 1% cross-reactivity with recombinant human (rh) LIPG, rhLIPI, and rhPNLIPRP1 is observed.
Reconstitute in sterile PBS to a final concentration of 0.2 mg/mL.
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: alpha lipase; Lipoprotein lipase; LPL; O 1-4-5; Phospholipase A1
基因别名: HDLCQ11; LIPD; LPL
UniProt ID: (Human) P06858, (Mouse) P11152
Entrez Gene ID: (Human) 4023, (Mouse) 16956