Lipoprotein lipase (LPL) Mouse Monoclonal Antibody [Clone ID: LBI4G7]
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
Lipoprotein lipase
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
Concentration
0.82 mg/ml
Dilution
WB 1:2000, IHC 1:150, IF 1:100
Form
PBS (PH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.
Buffer
PBS (PH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.
Function
Druggable Genome
Storage Conditions
Store 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
LPL (Lipoprotein lipase) mouse monoclonal antibody, clone LBI4G7
Gene ID URL
https://www.ncbi.nlm.nih.gov/gene/?term=4023
Uniprot URL
https://www.uniprot.org/uniprot/P06858
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