Acyl-CoA Dehydrogenase, C-4 To C-12 Straight Chain (ACADM)
Spezies
Human
Quelle
Synthetic
Applikation
Blocking Peptide (BP), Western Blotting (WB)
Produktmerkmale
This is a synthetic peptide designed for use in combination with anti-ACADM antibody (Catalog #: ARP32788_P050). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
Each Investigator should determine their own optimal working dilution for specific applications.
Beschränkungen
Nur für Forschungszwecke einsetzbar
Format
Lyophilized
Rekonstitution
Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
Konzentration
1 mg/mL
Buffer
Final peptide concentration is 1 mg/mL in PBS.
Handhabung
Avoid repeated freeze-thaw cycles.
Lagerung
-20 °C
Informationen zur Lagerung
For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
Target
Acyl-CoA Dehydrogenase, C-4 To C-12 Straight Chain (ACADM)
Synonyme
ACAD1 Peptide, MCAD Peptide, MCADH Peptide, AU018656 Peptide, fb53e01 Peptide, wu:fb53e01 Peptide, zgc:111905 Peptide, zgc:56101 Peptide, zgc:76911 Peptide, acyl-CoA dehydrogenase medium chain Peptide, acyl-CoA dehydrogenase, C-4 to C-12 straight chain L homeolog Peptide, acyl-Coenzyme A dehydrogenase, medium chain Peptide, acyl-CoA dehydrogenase, C-4 to C-12 straight chain Peptide, ACADM Peptide, acadm.L Peptide, Acadm Peptide, acadm Peptide
Hintergrund
ACADM Is the medium-chain specific (C4 to C12 straight chain) acyl-Coenzyme A dehydrogenase. The homotetramer enzyme catalyzes the initial step of the mitochondrial fatty acid beta-oxidation pathway. Clinical phenotypes are associated with ACADM hereditary deficiency.This gene encodes the medium-chain specific (C4 to C12 straight chain) acyl-Coenzyme A dehydrogenase. The homotetramer enzyme catalyzes the initial step of the mitochondrial fatty acid beta-oxidation pathway. Defects in this gene cause medium-chain acyl-CoA dehydrogenase deficiency, a disease characterized by hepatic dysfunction, fasting hypoglycemia, and encephalopathy, which can result in infantile death. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
Alias Symbols: ACAD1, MCAD, MCADH
Protein Interaction Partner: ACADM,SUMO4,USP20,USP50