Lipoprotein Lipase anticorps

N° du produit ABIN969262

Cet anticorps Souris Monoclonal détecte spécifiquement Lipoprotein Lipase dans WB et ELISA. Il présente une réactivité envers Humain et a été mentionné dans 2+ publications.

Aperçu rapide pour Lipoprotein Lipase anticorps (ABIN969262)

Antigène: Lipoprotein Lipase (LPL)

Reactivité: Humain

Hôte: Souris

Clonalité: Monoclonal

Conjugué: Cet anticorp Lipoprotein Lipase est non-conjugé

Application: Western Blotting (WB), ELISA

Clone: 2C5

Détail du produit anti-Lipoprotein Lipase anticorps

Fonction: LPL Antibody

Purification: Ascitic fluid

Immunogène: Purified recombinant fragment of LPL expressed in E. Coli.

Isotype: IgG1

Information d'application

Indications d'application: ELISA: 1/10000

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Ascitic fluid containing 0.03 % sodium azide.

Agent conservateur: Sodium azide

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

Stock: 4 °C,-20 °C

Stockage commentaire: Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.

Références pour anticorps anti-Lipoprotein Lipase (ABIN969262)

Chen, Jou, Fann, Chen, Chung, Lin, Wu, Kang, Chen, Jong, Lo, Kang, Chen, Chang, Huang, Wu, Pan: "Lipoprotein lipase variants associated with an endophenotype of hypertension: hypertension combined with elevated triglycerides." dans: Human mutation, Vol. 30, Issue 1, pp. 49-55, (2009) (PubMed).

Berk, Johnson, Lee, Zhang, Boozer, Pi-Sunyer, Fried, Albu: "Higher post-absorptive skeletal muscle LPL activity in African American vs. non-Hispanic White pre-menopausal women." dans: Obesity (Silver Spring, Md.), Vol. 16, Issue 1, pp. 199-201, (2008) (PubMed).

Détails sur Lipoprotein Lipase

Antigène: Lipoprotein Lipase (LPL)

Autre désignation: LPL

Sujet: LPL: lipoprotein lipase, also known as LIPD, HDLCQ11. Entrez Protein: NP_000228. It 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.

Poids moléculaire: 53.1 kDa

UniProt: P06858

Pathways: Lipid Metabolism