Non disponible en dehors du Royaume-Uni et de l'Irlande
General description
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.
Immunogen
Recombinant fusion protein containing a sequence corresponding to amino acids 124-475 of human LPL (NP_000228.1).
Physical form
PBS with 0.02% sodium azide,50% glycerol,pH7.3.
Storage and Stability
Store at -20℃. Avoid freeze / thaw cycles.
Ce produit répond aux critères suivants pour être admissible aux récompenses suivantes :