Lipase A Antikörper (truncated)

Produktnummer ABIN2464075

Produktdetails anti-Lipase A Antikörper

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

Bindungsspezifität: truncated

Reaktivität: Human

Wirt: Maus

Klonalität: Monoklonal

Konjugat: Dieser Lipase A Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), ELISA

Aufreinigung: Antibody is purified by protein A affinity chromatography.

Immunogen: Ni-NTA purified truncated recombinant LAL expressed in E. Coli strain BL21 (DE3).

Klon: 9G7F12

Isotyp: IgG2a

Anwendungsinformationen

Applikationshinweise: Western Blot:Dilution 1:500 - 1:2,000
ELISA:Propose dilution 1:10,000.
Determining optimal working dilutions by titration test.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Buffer: Purified antibody 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: As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.

Lagerung: -20 °C

Informationen zur Lagerung: LAL monoclonal antibody can be stored at -20 °C, stable for one year.

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: Lysosomal acid lipase (LAL), with 378-amino acid protein( 43-54 kDa), 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.

Gen-ID: 3988

UniProt: P38571