Lipoprotein lipase (LPL) Mouse Monoclonal Antibody [Clone ID: LBI3A10]
Product Specifications
Background
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]
Synonyms
HDLCQ11; LIPD
Gene Name
Homo sapiens lipoprotein lipase (LPL), mRNA.
Gene ID
4023
UniProt
P06858
Conjugation
Unconjugated
Related Pathways
Alzheimer's disease, Glycerolipid metabolism, PPAR signaling pathway
Field of Research
Alzheimer's disease, Glycerolipid metabolism, PPAR signaling pathway
Dilution
WB 1:500, IHC 1:150, FLOW 1:100
Form
Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)
Buffer
Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)
Function
Druggable Genome
Storage Conditions
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.
Symbol
LPL
Overview
Carrier-free (BSA/glycerol-free) LPL mouse monoclonal antibody, clone LBI3A10
Gene ID URL
https://www.ncbi.nlm.nih.gov/gene/?term=4023
Uniprot URL
https://www.uniprot.org/uniprot/P06858
Curated Selection
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