Lipoprotein Lipase Antikörper

Produktnummer ABIN2854941

Dieses Anti-Lipoprotein Lipase-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von Lipoprotein Lipase in WB, ICC, IF und IHC (p). Geeignet für Human.

Kurzübersicht für Lipoprotein Lipase Antikörper (ABIN2854941)

Target: Lipoprotein Lipase (LPL)

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser Lipoprotein Lipase Antikörper ist unkonjugiert

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

Produktdetails anti-Lipoprotein Lipase Antikörper

Kreuzreaktivität: Huhn, Human, Maus, Schaf

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

Aufreinigung: Purified by antigen-affinity chromatography.

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

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: 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.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 0.11 mg/mL

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

Konservierungsmittel: ProClin

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

Lagerung: 4 °C,-20 °C

Informationen zur Lagerung: 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.

Details zu Lipoprotein Lipase

Target: Lipoprotein Lipase (LPL)

Andere Bezeichnung: lipoprotein lipase

Hintergrund: 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

Molekulargewicht: 53 kDa

Gen-ID: 4023

UniProt: P06858

Pathways: Lipid Metabolism