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PRPS1 antibody (AA 1-318)

This anti-PRPS1 antibody is a Mouse Monoclonal antibody detecting PRPS1 in WB, ELISA, IF and ICC. Suitable for Human.
Catalog No. ABIN7596089

Quick Overview for PRPS1 antibody (AA 1-318) (ABIN7596089)

Target

See all PRPS1 Antibodies
PRPS1 (phosphoribosyl Pyrophosphate Synthetase 1 (PRPS1))

Reactivity

  • 9
  • 2
  • 1
Human

Host

  • 6
  • 3
Mouse

Clonality

  • 7
  • 2
Monoclonal

Conjugate

  • 9
This PRPS1 antibody is un-conjugated

Application

  • 9
  • 5
  • 3
  • 3
  • 2
  • 2
  • 2
Western Blotting (WB), ELISA, Immunofluorescence (IF), Immunocytochemistry (ICC)

Clone

AT1E11
  • Binding Specificity

    • 4
    • 2
    • 1
    AA 1-318

    Purpose

    Human PRPS1 antibody

    Purification

    protein-A affinity chromatography

    Immunogen

    Recombinant human PRPS1 (1-318aa) purified from E. coli

    Isotype

    IgG2a kappa
  • 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

    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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