LPL (clone 2C5), anti-human
€478.00
In stock
SKU
252872
Protein Family: Enzymes
Pathway and Disease: Lipid Metabolism
Description:
LPL (Lipoprotein lipase) is expressed in heart, muscle and adipose tissue. LPL functions as a homodimer and has 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.
Alternate Names: LIPD, HDLCQ11, Lipoprotein lipase, LPL
Application Notes: WB: 1:500-1:2000
Accession No.: P06858
Antigen: Purified recombinant fragment of LPP expressed in E. coli.
Format: Each vial contains 0.1 ml ascitic fluid with 0.03% sodium azide.
Storage:
Store at 4°C for short term use only. Store at -20°C for storage over 1 month. Product is guaranteed 6 months from the date of shipment.
Pathway and Disease: Lipid Metabolism
Description:
LPL (Lipoprotein lipase) is expressed in heart, muscle and adipose tissue. LPL functions as a homodimer and has 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.
Alternate Names: LIPD, HDLCQ11, Lipoprotein lipase, LPL
Application Notes: WB: 1:500-1:2000
Accession No.: P06858
Antigen: Purified recombinant fragment of LPP expressed in E. coli.
Format: Each vial contains 0.1 ml ascitic fluid with 0.03% sodium azide.
Storage:
Store at 4°C for short term use only. Store at -20°C for storage over 1 month. Product is guaranteed 6 months from the date of shipment.
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