APOA1 anticorps (C-Term)

N° du produit ABIN6991518

Cet anticorps anti-APOA1 est un anticorps Lapin Polyclonal détectant APOA1 dans WB et ELISA. Adapté pour Humain et Poulet.

Aperçu rapide pour APOA1 anticorps (C-Term) (ABIN6991518)

Antigène: APOA1 (Apolipoprotein A-I (APOA1))

Reactivité: Humain, Poulet

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp APOA1 est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-APOA1 anticorps

Épitope: C-Term

Purification: ApoA1 Antibody is affinity chromatography purified via peptide column.

Immunogène: ApoA1 antibody was raised against a 19 amino acid synthetic peptide near the carboxy terminus of human ApoA1. The immunogen is located within the last 50 amino acids of ApoA1.

Isotype: IgG

Information d'application

Indications d'application: ApoA1 antibody can be used for detection of ApoA1 by Western blot at 1 μ,g/mL.

Antibody validated: Western Blot in chicken samples. All other applications and species not yet tested.

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: ApoA1 Antibody is supplied in PBS containing 0.02 % 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: -20 °C,4 °C

Stockage commentaire: ApoA1 antibody can be stored at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.

Détails sur APOA1

Antigène: APOA1 (Apolipoprotein A-I (APOA1))

Autre désignation: ApoA1

Sujet: ApoA1 Antibody: Apolipoprotein A1 (ApoA1) is the major protein component of high density lipoprotein (HDL) in plasma, which is correlated with cardiovascular disease. ApoA1 is synthesized in the liver and small intestine and promotes cholesterol efflux from tissues to the liver for excretion. It is a cofactor for lecithin cholesterolacyltransferase (LCAT), the enzyme responsible for the formation of most plasma cholesteryl esters. Defects in ApoA1 are associated with HDL deficiency, Tangier disease, and systemic non-neuropathic amyloidosis.

ID gène: 335

UniProt: P02647

Pathways: Regulation of Lipid Metabolism by PPARalpha, Production of Molecular Mediator of Immune Response, Lipid Metabolism