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alpha-Methylacyl-CoA Racemase (AMACR) (C-Term) Peptid

AMACR Reaktivität: Human Wirt: Synthetic BP, WB, IHC
Produktnummer ABIN8094470
168,15 €
Zzgl. Versandkosten 20,00 € und MwSt
100 μg
Lieferung nach: Deutschland
Lieferung in 6 bis 9 Werktagen

Kurzübersicht für alpha-Methylacyl-CoA Racemase (AMACR) (C-Term) Peptid (ABIN8094470)

Target

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

Spezies

Human

Quelle

  • 10
Synthetic

Applikation

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

    C-Term

    Verwendungszweck

    AMACR Peptide - C-terminal region

    Sequenz

    IFDGTDACVT PVLTFEEVVH HDHNKERGSF ITSEEQDVSP RPAPLLLNTP
  • Applikationshinweise

    Optimal working dilution should be determined by the investigator.

    Kommentare

    This is a synthetic peptide designed for use in combination with anti-AMACR Antibody (ARP60806_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.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Rekonstitution

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

    Buffer

    Lyophilized powder

    Lagerung

    -20 °C

    Informationen zur Lagerung

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

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

    Hintergrund

    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

    Molekulargewicht

    42kDa

    Gen-ID

    23600

    NCBI Accession

    NP_055139

    UniProt

    Q9UHK6
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