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APRT antibody (AA 5-49)

This anti-APRT antibody is a Rabbit Polyclonal antibody detecting APRT in WB and FACS. Suitable for Human.
Catalog No. ABIN5647397

Quick Overview for APRT antibody (AA 5-49) (ABIN5647397)

Target

See all APRT Antibodies
APRT (Adenine Phosphoribosyltransferase (APRT))

Reactivity

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

Host

  • 50
  • 4
Rabbit

Clonality

  • 52
  • 2
Polyclonal

Conjugate

  • 33
  • 3
  • 3
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This APRT antibody is un-conjugated

Application

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

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

    Purification

    Antigen affinity purified

    Immunogen

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

    Isotype

    IgG
  • 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

    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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