Telefon:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@antikoerper-online.de

Ornithine Aminotransferase (OAT) (Middle Region) Peptid

OAT Reaktivität: Human Wirt: Synthetic BP, WB
Produktnummer ABIN981078
  • Target Alle OAT Produkte
    OAT (Ornithine Aminotransferase (OAT))
    Protein Region
    Middle Region
    Spezies
    Human
    Quelle
    • 4
    • 1
    Synthetic
    Applikation
    Blocking Peptide (BP), Western Blotting (WB)
    Produktmerkmale
    This is a synthetic peptide designed for use in combination with anti-OAT antibody (Catalog #: ARP48134_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.
    Aufreinigung
    Purified
  • Applikationshinweise
    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
    OAT (Ornithine Aminotransferase (OAT))
    Hintergrund
    OAT is a key enzyme in the pathway that converts arginine and ornithine into the major excitatory and inhibitory neurotransmitters glutamate and GABA. Mutations of this enzyme cause the autosomal recessive eye disease Gyrate Atrophy. This gene encodes the mitochondrial enzyme ornithine aminotransferase, which is a key enzyme is the pathway that converts arginine and ornithine into the major excitatory and inhibitory neurotransmitters glutamate and GABA. Mutations that result in a deficiency of this enzyme cause the autosomal recessive eye disease Gyrate Atrophy. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications. PRIMARYREFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-42 DB459793.1 27-68 43-2062 BC016928.1 1-2020 2063-2066 M12267.1 2010-2013

    Alias Symbols: DKFZp781A11155, HOGA, OKT, GACR, OATASE

    Protein Interaction Partner: C2orf18,OAT,UBQLN4,C2orf18,DMWD,EIF6,OTUD4

    Protein Size: 439
    Molekulargewicht
    45 kDa
    Gen-ID
    4942
    NCBI Accession
    NM_000274, NP_000265
    UniProt
    P04181
Sie sind hier:
Kundenservice