ACADL Antikörper

Produktnummer ABIN2458052

Produktdetails anti-ACADL Antikörper

Target: ACADL (Acyl-CoA Dehydrogenase, Long Chain (ACADL))

Reaktivität: Human, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser ACADL Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), ELISA

Aufreinigung: Antibody is purified by peptide affinity chromatography method.

Immunogen: Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human ACADL.

Anwendungsinformationen

Applikationshinweise: ACADL antibody can be used for detection of ACADL by ELISA at 1:312500. ACADL antibody can be used for detection of ACADL by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Lyophilized

Rekonstitution: Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.

Konzentration: 1 mg/mL

Buffer: Antibody is lyophilized in PBS buffer with 2 % sucrose.

Handhabung: As with any antibody avoid repeat freeze-thaw cycles.

Lagerung: 4 °C/-20 °C

Informationen zur Lagerung: For short periods of storage (days) store at 4 °C. For longer periods of storage, store ACADL antibody at -20 °C.

Details zu ACADL

Target: ACADL (Acyl-CoA Dehydrogenase, Long Chain (ACADL))

Andere Bezeichnung: ACADL (ACADL Produkte)

Synonyme: zgc:55656 antikoerper, ACAD4 antikoerper, LCAD antikoerper, ACOADA antikoerper, AA960361 antikoerper, AU018452 antikoerper, C79855 antikoerper, acyl-CoA dehydrogenase long chain antikoerper, acyl-CoA dehydrogenase, long chain antikoerper, acyl-CoA dehydrogenase, long chain L homeolog antikoerper, acyl-Coenzyme A dehydrogenase, long-chain antikoerper, acadl antikoerper, ACADL antikoerper, Acadl antikoerper, acadl.L antikoerper

Hintergrund: ACADL belongs to the acyl-CoA dehydrogenase family, which is a family of mitochondrial flavoenzymes involved in fatty acid and branched chain amino-acid metabolism. This protein is one of the four enzymes that catalyze the initial step of mitochondrial beta-oxidation of straight-chain fatty acid. Defects in this gene are the cause of long-chain acyl-CoA dehydrogenase (LCAD) deficiency, leading to nonketotic hypoglycemia.The protein encoded by this gene belongs to the acyl-CoA dehydrogenase family, which is a family of mitochondrial flavoenzymes involved in fatty acid and branched chain amino-acid metabolism. This protein is one of the four enzymes that catalyze the initial step of mitochondrial beta-oxidation of straight-chain fatty acid. Defects in this gene are the cause of long-chain acyl-CoA dehydrogenase (LCAD) deficiency, leading to nonketotic hypoglycemia.

Molekulargewicht: 44 kDa

Gen-ID: 33

NCBI Accession: NP_001599

UniProt: P28330

Pathways: Monocarboxylic Acid Catabolic Process