Lipoproteïnelipase (LPL) Mouse Monoclonal Antibody [Clone ID: LBI4H3]

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]

Carrier-free (BSA/glycerol-free) LPL mouse monoclonal antibody, clone LBI4H3

HDLCQ11; LIPD

Homo sapiens lipoprotein lipase (LPL), mRNA.

4023

P06858

Unconjugated

Alzheimer's disease, Glycerolipid metabolism, PPAR signaling pathway

Alzheimer's disease, Glycerolipid metabolism, PPAR signaling pathway

WB 1:2000, IHC 1:150

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

Druggable Genome

Stable for 1 year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. Aliquot will be stable at 4°C short term. For long-term storage, aliquot and store at -20°C or below. Stable for 12 months at -20°C. Avoid repeated freeze-thaw cycles.

LPL

https://www.ncbi.nlm.nih.gov/gene/?term=4023

https://www.uniprot.org/uniprot/P06858