Lipoprotein Lipase anticorps

N° du produit ABIN2854941

Cet anticorps anti-Lipoprotein Lipase est un anticorps Lapin Polyclonal détectant Lipoprotein Lipase dans WB, ICC, IF et IHC (p). Adapté pour Humain.

Aperçu rapide pour Lipoprotein Lipase anticorps (ABIN2854941)

Antigène: Lipoprotein Lipase (LPL)

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Lipoprotein Lipase est non-conjugé

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

Détail du produit anti-Lipoprotein Lipase anticorps

Réactivité croisée: Poulet, Humain, Souris, Mouton

Attributs du produit: Rabbit Polyclonal antibody to LPL (lipoprotein lipase)
LPL antibody

Purification: Purified by antigen-affinity chromatography.

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

Isotype: IgG

Information d'application

Indications d'application: 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

Stockage

Format: Liquid

Concentration: 0.11 mg/mL

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

Agent conservateur: ProClin

Précaution d'utilisation: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: 4 °C,-20 °C

Stockage commentaire: 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.

Détails sur Lipoprotein Lipase

Antigène: Lipoprotein Lipase (LPL)

Autre désignation: lipoprotein lipase

Sujet: 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

Poids moléculaire: 53 kDa

ID gène: 4023

UniProt: P06858

Pathways: Lipid Metabolism