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APRT Antikörper (AA 5-49)

Dieses Anti-APRT-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von APRT in WB und FACS. Geeignet für Human.
Produktnummer ABIN5647397

Kurzübersicht für APRT Antikörper (AA 5-49) (ABIN5647397)

Target

Alle APRT Antikörper anzeigen
APRT (Adenine Phosphoribosyltransferase (APRT))

Reaktivität

  • 54
  • 6
  • 3
  • 2
  • 1
  • 1
Human

Wirt

  • 50
  • 4
Kaninchen

Klonalität

  • 52
  • 2
Polyklonal

Konjugat

  • 33
  • 3
  • 3
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser APRT Antikörper ist unkonjugiert

Applikation

  • 41
  • 24
  • 19
  • 11
  • 10
  • 8
  • 7
  • 6
  • 4
  • 2
  • 2
  • 1
Western Blotting (WB), Flow Cytometry (FACS)
  • Bindungsspezifität

    • 15
    • 8
    • 7
    • 6
    • 3
    • 1
    • 1
    • 1
    • 1
    AA 5-49

    Aufreinigung

    Antigen affinity purified

    Immunogen

    Amino acids 5-49 (ELQLVEQRIRSFPDFPTPGVVFRDISPVLKDPASFRAAIGLLARH-human) were used as the immunogen for the APRT antibody.

    Isotyp

    IgG
  • Applikationshinweise

    Optimal dilution of the APRT antibody should be determined by the researcher.\. Western blot: 0.5-1 μg/mL,FACS: 1-3 μg/10^6 cells

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Lagerung

    -20 °C

    Informationen zur Lagerung

    After reconstitution, the APRT antibody can be stored for up to one month at 4°C. For long-term, aliquot and store at -20°C. Avoid repeated freezing and thawing.
  • Target

    APRT (Adenine Phosphoribosyltransferase (APRT))

    Andere Bezeichnung

    APRT

    Hintergrund

    Adenine phosphoribosyltransferase (APRTase) is an enzyme encoded by the APRT gene, found in humans on chromosome 16. It belongs to the purine/pyrimidine phosphoribosyltransferase family. A conserved feature of this gene is the distribution of CpG dinucleotides. This enzyme catalyzes the formation of AMP and inorganic pyrophosphate from adenine and 5-phosphoribosyl-1-pyrophosphate (PRPP). It also produces adenine as a by-product of the polyamine biosynthesis pathway. A homozygous deficiency in this enzyme causes 2,8-dihydroxyadenine urolithiasis. Two transcript variants encoding different isoforms have been found for this gene.

    UniProt

    P07741

    Pathways

    Ribonucleoside Biosynthetic Process
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