ACADL Antikörper (N-Term)

Produktnummer ABIN1105201

Produktdetails anti-ACADL Antikörper

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

Bindungsspezifität: N-Term

Reaktivität: Human, Maus, Ratte, Schwein, Rind (Kuh)

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser ACADL Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Sequenz: MAARLLRGSL RVLGGHRAPR QLPAARCSHS GGEERLETPS AKKLTDIGIR

Kreuzreaktivität (Details): Species reactivity (expected):Mouse, Rat, Pig, BovineSpecies reactivity (tested):Human

Aufreinigung: Purified using peptide immunoaffinity column

Immunogen: The immunogen for anti-ACADL antibody: synthetic peptide directed towards the N terminal of human ACADL

Anwendungsinformationen

Applikationshinweise: Optimal working dilution should be determined by the investigator.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Rekonstitution: Add 50 μL of distilled water to a final concentration of 1 mg/mL.

Handhabung: Avoid repeated freezing and thawing.

Lagerung: 4 °C/-20 °C

Informationen zur Lagerung: Store lyophilized at 2-8 °C or at -20 °C long term. After reconstitution store the antibody undiluted at 2-8 °C for up to one month or in aliquots at -20 °C long term.

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 ACADL 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.Synonyms: LCAD, Long-chain specific acyl-CoA dehydrogenase, mitochondrial

Gen-ID: 33

NCBI Accession: NP_001599

Pathways: Monocarboxylic Acid Catabolic Process