ARG41455

anti-LPL / Lipoprotein Lipase antibody

anti-LPL / Lipoprotein Lipase antibody for IHC-Formalin-fixed paraffin-embedded sections,Western blot and Human

Overview

Product Description Rabbit Polyclonal antibody recognizes LPL / Lipoprotein Lipase
Tested Reactivity Hu
Tested Application IHC-P, WB
Host Rabbit
Clonality Polyclonal
Isotype IgG
Target Name LPL / Lipoprotein Lipase
Antigen Species Human
Immunogen Synthetic peptide of Human LPL / Lipoprotein Lipase.
Conjugation Un-conjugated
Alternate Names EC 3.1.1.34; LPL; Lipoprotein lipase; LIPD; HDLCQ11

Application Instructions

Application Suggestion
Tested Application Dilution
IHC-P1:50 - 1:200
WB1:1000 - 1:5000
Application Note * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.
Positive Control Human fetal liver
Observed Size ~ 55 kDa

Properties

Form Liquid
Purification Affinity purified.
Buffer PBS (pH 7.4), 150 mM NaCl, 0.02% Sodium azide and 50% Glycerol.
Preservative 0.02% Sodium azide
Stabilizer 50% Glycerol
Storage Instruction For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
Note For laboratory research only, not for drug, diagnostic or other use.

Bioinformation

Database Links

GeneID: 4023 Human LPL

Swiss-port # P06858 Human Lipoprotein lipase

Gene Symbol LPL
Gene Full Name lipoprotein lipase
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, Jul 2008]
Function The primary function of this lipase is the hydrolysis of triglycerides of circulating chylomicrons and very low density lipoproteins (VLDL). Binding to heparin sulfate proteogylcans at the cell surface is vital to the function. The apolipoprotein, APOC2, acts as a coactivator of LPL activity in the presence of lipids on the luminal surface of vascular endothelium (By similarity). [UniProt]
Cellular Localization Cell membrane; Lipid-anchor, GPI-anchor. Secreted. Note=Locates to the plasma membrane of microvilli of hepatocytes with triacyl-glycerol-rich lipoproteins (TRL). Some of the bound LPL is then internalized and located inside non-coated endocytic vesicles (By similarity). [UniProt]
Calculated MW 53 kDa
PTM Tyrosine nitration after lipopolysaccharide (LPS) challenge down-regulates the lipase activity. [UniProt]

Images (1) Click the Picture to Zoom In

  • ARG41455 anti-LPL / Lipoprotein Lipase antibody WB image

    Western blot: Human fetal liver lysate stained with ARG41455 anti-LPL / Lipoprotein Lipase antibody.