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