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PRPS1 antibody (AA 1-318)

PRPS1 Reactivity: Human WB, ELISA, IF, ICC Host: Mouse Monoclonal AT1E11 unconjugated
Catalog No. ABIN7596089
  • Target See all PRPS1 Antibodies
    PRPS1 (phosphoribosyl Pyrophosphate Synthetase 1 (PRPS1))
    Binding Specificity
    • 4
    • 2
    • 1
    AA 1-318
    Reactivity
    • 10
    • 3
    • 2
    Human
    Host
    • 7
    • 3
    Mouse
    Clonality
    • 8
    • 2
    Monoclonal
    Conjugate
    • 10
    This PRPS1 antibody is un-conjugated
    Application
    • 10
    • 5
    • 3
    • 3
    • 2
    • 2
    • 2
    Western Blotting (WB), ELISA, Immunofluorescence (IF), Immunocytochemistry (ICC)
    Purpose
    Human PRPS1 antibody
    Purification
    protein-A affinity chromatography
    Immunogen
    Recombinant human PRPS1 (1-318aa) purified from E. coli
    Clone
    AT1E11
    Isotype
    IgG2a kappa
    Top Product
    Discover our top product PRPS1 Primary Antibody
  • Application Notes
    Optimal working dilution should be determined by the investigator.
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 mg/mL
    Buffer
    Phosphate-Buffered Saline (pH 7.4) with 0.02% Sodium Azide, 10% glycero
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    4 °C,-20 °C,-80 °C
    Storage Comment
    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))
    Alternative Name
    PRPS1 (PRPS1 Products)
    Background
    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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