ACADL anticorps (N-Term)

N° du produit ABIN1105201

Détail du produit anti-ACADL anticorps

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

Épitope: N-Term

Reactivité: Humain, Souris, Rat, Porc, Boeuf (Vache)

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp ACADL est non-conjugé

Application: Western Blotting (WB)

Séquence: MAARLLRGSL RVLGGHRAPR QLPAARCSHS GGEERLETPS AKKLTDIGIR

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

Purification: Purified using peptide immunoaffinity column

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

Information d'application

Indications d'application: Optimal working dilution should be determined by the investigator.

Restrictions: For Research Use only

Stockage

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

Conseil sur la manipulation: Avoid repeated freezing and thawing.

Stock: 4 °C/-20 °C

Stockage commentaire: 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.

Détails sur ACADL

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

Autre désignation: ACADL (ACADL Produits)

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

Sujet: 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

ID gène: 33

NCBI Accession: NP_001599

Pathways: Monocarboxylic Acid Catabolic Process