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Medium-Chain Specific Acyl-CoA Dehydrogenase, Mitochondrial (MCAD) (Middle Region) Peptide

MCAD Reactivité: Souris Hôte: Synthetic BP
N° du produit ABIN8105039
168,15 €
Plus frais de livraison 40,00 € et TVA
100 μg
Destination: France
Envoi sous 6 à 9 jours ouvrables

Aperçu rapide pour Medium-Chain Specific Acyl-CoA Dehydrogenase, Mitochondrial (MCAD) (Middle Region) Peptide (ABIN8105039)

Antigène

Medium-Chain Specific Acyl-CoA Dehydrogenase, Mitochondrial (MCAD)

Origine

Souris

Source

  • 6
Synthetic

Application

Blocking Peptide (BP)
  • Protein Region

    Middle Region

    Fonction

    ACADM Peptide - middle region

    Séquence

    FDACLITEEL AYGCTGVQTA IEANSLGQMP VILAGNDQQK KKYLGRMTEQ
  • Indications d'application

    Optimal working dilution should be determined by the investigator.

    Commentaires

    This is a synthetic peptide designed for use in combination with anti- ACADM Antibody (ARP89968_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. Please inquire for more details.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Add 100 µL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.

    Buffer

    Lyophilized powder

    Stock

    -20 °C

    Stockage commentaire

    For longer periods of storage, store at -20 °C. Avoid repeat freeze-thaw cycles.
  • Antigène

    Medium-Chain Specific Acyl-CoA Dehydrogenase, Mitochondrial (MCAD)

    Sujet

    Background Information: This gene encodes a homotetrameric mitochondrial flavoprotein and is a member of the acyl-CoA dehydrogenase family. Members of this family catalyze the first step of fatty acid beta-oxidation, forming a C2-C3 trans-double bond in a FAD-dependent reaction. As beta-oxidation cycles through its four steps, each member of the acyl-CoA dehydrogenase family works at an optimum fatty acid chain-length. This enzyme has its optimum length between C6- and C12-acylCoA. In mice, deficiency of this gene can cause neonatal mortality as well as fasting and cold intolerance. This gene has multiple, intronless pseudogenes.

    Alternative Symbols: MCAD, AU018656

    Poids moléculaire

    46 kDa

    ID gène

    11364

    NCBI Accession

    NP_031408

    UniProt

    P45952
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