Lipase A Antikörper

Produktnummer ABIN3210008

Produktdetails anti-Lipase A Antikörper

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

Reaktivität: Human

Wirt: Maus

Klonalität: Monoklonal

Konjugat: Dieser Lipase A Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), ELISA

Aufreinigung: Purified antibody.

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

Klon: 9G7F12-7G6D7

Isotyp: IgG2a

Anwendungsinformationen

Applikationshinweise: ELISA: 1:10,000, WB: 1:500-1:2000,
Optimal conditions should be determined by the investigator.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Konzentration: Lot specific

Buffer: Purified antibody supplied in PBS containing 0.03 % sodium azide.

Konservierungsmittel: Sodium azide

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

Handhabung: Avoid repeated freeze/thaw cycles.
Dilute only prior to immediate use.

Lagerung: 4 °C/-20 °C

Informationen zur Lagerung: Store at 4 °C for short term storage. Store at -20 °C for long term storage.

Details zu Lipase A

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

Andere Bezeichnung: LAL (LIPA Produkte)

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

Hintergrund: 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.