Lipase A anticorps

N° du produit ABIN3210008

Détail du produit anti-Lipase A anticorps

Antigène: Lipase A (LIPA) (Lipase A, Lysosomal Acid, Cholesterol Esterase (LIPA))

Reactivité: Humain

Hôte: Souris

Clonalité: Monoclonal

Conjugué: Cet anticorp Lipase A est non-conjugé

Application: Western Blotting (WB), ELISA

Purification: Purified antibody.

Immunogène: LAL antibody was raised in Mouse using a purified recombinant fragment of LAL expressed in E. coli as the immunogen.

Clone: 9G7F12-7G6D7

Isotype: IgG2a

Information d'application

Indications d'application: ELISA: 1:10,000, WB: 1:500-1:2000,
Optimal conditions should be determined by the investigator.

Restrictions: For Research Use only

Stockage

Concentration: Lot specific

Buffer: Purified antibody supplied in PBS 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.

Conseil sur la manipulation: Avoid repeated freeze/thaw cycles.
Dilute only prior to immediate use.

Stock: 4 °C/-20 °C

Stockage commentaire: Store at 4 °C for short term storage. Store at -20 °C for long term storage.

Détails sur Lipase A

Antigène: Lipase A (LIPA) (Lipase A, Lysosomal Acid, Cholesterol Esterase (LIPA))

Autre désignation: LAL (LIPA Produits)

Synonymes: anticorps cesd, anticorps lal, anticorps LIPA, anticorps CESD, anticorps LAL, anticorps Chole, anticorps Chole2, anticorps Lip1, anticorps AA960673, anticorps Lal, anticorps Lip-1, anticorps lipase A, lysosomal acid type, anticorps lipase A, lysosomal acid, cholesterol esterase, anticorps lipase A, lysosomal acid, cholesterol esterase L homeolog, anticorps lysosomal acid lipase A, anticorps LIPA, anticorps lipa, anticorps lipa.L, anticorps Lipa

Sujet: LAL functions in the lysosome to catalyze the hydrolysis of cholesteryl esters and triglycerides which are taken up by receptor-mediated endocytosis. An inherited deficiency or low activity of human lysosomal acid lipase results in the intralysosomal storage of the respective lipid substrates. So it is also responsible for the rare conditions of Wolman disease and cholesteryl ester storage disease (CESD). As the enzyme is synthesized by all nucleated cells, lipid-laden cells are found in all organs, particularly in liver, spleen, the adrenal and the hemopoietic system, and in the intestine as well as in the lymph nodes, lungs, testes, and ovaries. Synonyms: Monoclonal LAL antibody, Anti-LAL antibody, Lysosomal acid lipase antibody.