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PRPS1 Antikörper (AA 1-318)

PRPS1 Reaktivität: Human WB, ELISA, IF, ICC Wirt: Maus Monoclonal AT1E11 unconjugated
Produktnummer ABIN7596089
  • Target Alle PRPS1 Antikörper anzeigen
    PRPS1 (phosphoribosyl Pyrophosphate Synthetase 1 (PRPS1))
    Bindungsspezifität
    • 4
    • 2
    • 1
    AA 1-318
    Reaktivität
    • 10
    • 3
    • 2
    Human
    Wirt
    • 7
    • 3
    Maus
    Klonalität
    • 8
    • 2
    Monoklonal
    Konjugat
    • 10
    Dieser PRPS1 Antikörper ist unkonjugiert
    Applikation
    • 10
    • 5
    • 3
    • 3
    • 2
    • 2
    • 2
    Western Blotting (WB), ELISA, Immunofluorescence (IF), Immunocytochemistry (ICC)
    Verwendungszweck
    Human PRPS1 antibody
    Aufreinigung
    protein-A affinity chromatography
    Immunogen
    Recombinant human PRPS1 (1-318aa) purified from E. coli
    Klon
    AT1E11
    Isotyp
    IgG2a kappa
    Top Product
    Discover our top product PRPS1 Primärantikörper
  • Applikationshinweise
    Optimal working dilution should be determined by the investigator.
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    1 mg/mL
    Buffer
    Phosphate-Buffered Saline (pH 7.4) with 0.02% Sodium Azide, 10% glycero
    Konservierungsmittel
    Sodium azide
    Vorsichtsmaßnahmen
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Lagerung
    4 °C,-20 °C,-80 °C
    Informationen zur Lagerung
    Can be stored at +2°C to +8°C for 1 week. For long term storage, aliquot and store at -20°C to -80°C. Avoid repeated freezing and thawing cycles.
  • Target
    PRPS1 (phosphoribosyl Pyrophosphate Synthetase 1 (PRPS1))
    Andere Bezeichnung
    PRPS1 (PRPS1 Produkte)
    Hintergrund
    PRPS1 is an enzyme that catalyzes the phosphoribosylation of ribose 5-phosphate to 5-phosphoribosyl-1-pyrophosphate, which is necessary for purine metabolism and nucleotide biosynthesis. A mutation in PRPS1 may result in PRPS superactivity, a disease characterized by gout and the overproductionof purine nucleotides, uric acid and PRPP. PRPS1 mutations can also lead to a reduction in PRPS1 activity resulting in ARTS syndrome or CMTX5 (Charcot-Marie-Tooth disease X-linked recessive type 5).
    NCBI Accession
    NP_002755
    Pathways
    Ribonucleoside Biosynthetic Process
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