Acyl-CoA Dehydrogenase, C-4 To C-12 Straight Chain (ACADM)
Origine
Humain
Source
Synthetic
Application
Blocking Peptide (BP), Western Blotting (WB)
Attributs du produit
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.
Restrictions
For Research Use only
Format
Lyophilized
Reconstitution
Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
Concentration
1 mg/mL
Buffer
Final peptide concentration is 1 mg/mL in PBS.
Conseil sur la manipulation
Avoid repeated freeze-thaw cycles.
Stock
-20 °C
Stockage commentaire
For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
Antigène
Acyl-CoA Dehydrogenase, C-4 To C-12 Straight Chain (ACADM)
Synonymes
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
Sujet
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