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]

Overview

Carrier-free (BSA/glycerol-free) LPL mouse monoclonal antibody, clone LBI3A10

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.