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Recombinant Human Hypoxanthine-guanine phosphoribosyltransferase (HPRT1)

ACP01445

Number
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Specifications


Cat.No ACP01445 Target NameHPRT1
FormLiquid or Lyophilized powderExpression SystemE.coli
Expression Range2-218aaMol Weight24.6 kDa
Protein LengthFull Length of Mature ProteinPurityGreater than 90% as determined by SDS-PAGE.
Storage Buffer5%-50% glycerol. Lyophilized powder form: the buffer before lyophilization is Tris/PBS-based buffer, 6% Trehalose, Liquid form: default storage buffer is Tris/PBS-based buffer, pH 8.0.

Immunogen Information


Target SpeciesHumanUniprot IDP00492
Background Information
  • Uniprot Id

    P00492

  • Target Species

    Human

  • Target Name

    HPRT1

  • Target Full Name

    Hypoxanthine-guanine phosphoribosyltransferase

  • Target Function

    Converts guanine to guanosine monophosphate, and hypoxanthine to inosine monophosphate. Transfers the 5-phosphoribosyl group from 5-phosphoribosylpyrophosphate onto the purine. Plays a central role in the generation of purine nucleotides through the purine salvage pathway.

  • Target Involvement

    Lesch-Nyhan syndrome (LNS); Gout HPRT-related (GOUT-HPRT)

  • Target Subcellular Location

    Cytoplasm.

  • Target Protein Families

    Purine/pyrimidine phosphoribosyltransferase family

  • Target Research Area

    Metabolism

  • Target Synonyms

    HGPRT; HGPRTase; HPRT 1; HPRT_HUMAN; HPRT1; Hypoxanthine guanine phosphoribosyltransferase ; Hypoxanthine phosphoribosyltransferase 1 (Lesch Nyhan syndrome); Hypoxanthine phosphoribosyltransferase 1; Hypoxanthine-guanine phosphoribosyltransferase

  • Target Background

    The protein encoded by this gene is a transferase, which catalyzes conversion of hypoxanthine to inosine monophosphate and guanine to guanosine monophosphate via transfer of the 5-phosphoribosyl group from 5-phosphoribosyl 1-pyrophosphate. This enzyme plays a central role in the generation of purine nucleotides through the purine salvage pathway. Mutations in this gene result in Lesch-Nyhan syndrome or gout.

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