Lipoprotein Lipase antibody

Catalog No. ABIN2854941

This anti-Lipoprotein Lipase antibody is a Rabbit Polyclonal antibody detecting Lipoprotein Lipase in WB, ICC, IF and IHC (p). Suitable for Human.

Quick Overview for Lipoprotein Lipase antibody (ABIN2854941)

Target: Lipoprotein Lipase (LPL)

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This Lipoprotein Lipase antibody is un-conjugated

Application: Western Blotting (WB), Immunocytochemistry (ICC), Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Product Details anti-Lipoprotein Lipase Antibody

Cross-Reactivity: Chicken, Human, Mouse, Sheep

Characteristics: Rabbit Polyclonal antibody to LPL (lipoprotein lipase)
LPL antibody

Purification: Purified by antigen-affinity chromatography.

Immunogen: Recombinant protein encompassing a sequence within the center region of human LPL. The exact sequence is proprietary.

Isotype: IgG

Application Details

Application Notes: WB: 1:500-1:3000. ICC/IF: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 0.11 mg/mL

Buffer: 1XPBS ( pH 7), 1 % BSA, 20 % Glycerol, 0.025 % ProClin 300

Preservative: ProClin

Precaution of Use: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: 4 °C,-20 °C

Storage Comment: Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.

Target Details for Lipoprotein Lipase

Target: Lipoprotein Lipase (LPL)

Alternative 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.

Cellular Localization: Cell membrane, Lipid-anchor , GPI-anchor , Secreted

Molecular Weight: 53 kDa

Gene ID: 4023

UniProt: P06858

Pathways: Lipid Metabolism