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APRT antibody (AA 5-49)

APRT Reactivity: Human WB, FACS Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN5647397
  • Target See all APRT Antibodies
    APRT (Adenine Phosphoribosyltransferase (APRT))
    Binding Specificity
    • 13
    • 8
    • 7
    • 6
    • 3
    • 1
    • 1
    • 1
    • 1
    AA 5-49
    Reactivity
    • 50
    • 6
    • 3
    • 2
    • 1
    • 1
    Human
    Host
    • 47
    • 3
    Rabbit
    Clonality
    • 49
    • 1
    Polyclonal
    Conjugate
    • 29
    • 3
    • 3
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This APRT antibody is un-conjugated
    Application
    • 37
    • 20
    • 18
    • 9
    • 8
    • 7
    • 7
    • 4
    • 2
    • 2
    • 2
    • 1
    Western Blotting (WB), Flow Cytometry (FACS)
    Purification
    Antigen affinity purified
    Immunogen
    Amino acids 5-49 (ELQLVEQRIRSFPDFPTPGVVFRDISPVLKDPASFRAAIGLLARH-human) were used as the immunogen for the APRT antibody.
    Isotype
    IgG
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    Discover our top product APRT Primary Antibody
  • Application Notes
    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
    Restrictions
    For Research Use only
  • Buffer
    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water
    Storage
    -20 °C
    Storage Comment
    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))
    Alternative Name
    APRT (APRT Products)
    Background
    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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