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alpha-Methylacyl-CoA Racemase (AMACR) (Middle Region) Peptide

AMACR Reactivité: Humain Hôte: Synthetic BP, WB
N° du produit ABIN8094471
168,15 €
Plus frais de livraison 40,00 € et TVA
100 μg
Destination: France
Envoi sous 6 à 9 jours ouvrables

Aperçu rapide pour alpha-Methylacyl-CoA Racemase (AMACR) (Middle Region) Peptide (ABIN8094471)

Antigène

AMACR (alpha-Methylacyl-CoA Racemase (AMACR))

Origine

Humain

Source

  • 10
Synthetic

Application

Blocking Peptide (BP), Western Blotting (WB)
  • Protein Region

    Middle Region

    Fonction

    AMACR Peptide - middle region

    Séquence

    SGENPYAPLN LLADFAGGGL MCALGIIMAL FDRTRTGKGQ VIDANMVEGT
  • 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-AMACR Antibody (ARP60807_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

    AMACR (alpha-Methylacyl-CoA Racemase (AMACR))

    Sujet

    Background Information: This gene encodes a racemase. The encoded enzyme interconverts pristanoyl-CoA and C27-bile acylCoAs between their (R)- and (S)-stereoisomers. The conversion to the (S)-stereoisomers is necessary for degradation of these substrates by peroxisomal beta-oxidation. Encoded proteins from this locus localize to both mitochondria and peroxisomes. Mutations in this gene may be associated with adult-onset sensorimotor neuropathy, pigmentary retinopathy, and adrenomyeloneuropathy due to defects in bile acid synthesis. Alternatively spliced transcript variants have been described. Read-through transcription also exists between this gene and the upstream neighboring C1QTNF3 (C1q and tumor necrosis factor related protein 3) gene.

    Alternative Symbols: CBAS4, RACE, RM, AMACRD

    Poids moléculaire

    43kDa

    ID gène

    23600

    NCBI Accession

    NP_001161067

    UniProt

    F8W9N1
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