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Recombinant Human Thiopurine S-methyltransferase (TPMT), Truncated

ACP03072

Number
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Specifications


Cat.No ACP03072 Target NameTPMT
Target SynonymsHGNC:12014; S adenosyl L methionine thiopurine S methyltransferase; Thiopurine methyltransferase; Thiopurine S methyltransferase; Thiopurine S-methyltransferase; TPMT; TPMT_HUMANFormLiquid or Lyophilized powder
Expression SystemE.coliExpression Range4-244aa
Mol Weight54.7kDaProtein LengthPartial
PurityGreater 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 IDP51580
Background Information
  • Uniprot Id

    P51580

  • Target Species

    Human

  • Target Name

    TPMT

  • Target Full Name

    Thiopurine S-methyltransferase

  • Target Function

    Catalyzes the S-methylation of thiopurine drugs such as 6-mercaptopurine (also called mercaptopurine, 6-MP or its brand name Purinethol) and 6-thioguanine (also called tioguanine or 6-TG) using S-adenosyl-L-methionine as the methyl donor. TPMT activity modulates the cytotoxic effects of thiopurine prodrugs. A natural substrate for this enzyme has yet to be identified.

  • Target Subcellular Location

    Cytoplasm.

  • Target Protein Families

    Class I-like SAM-binding methyltransferase superfamily, TPMT family

  • Target Research Area

    Metabolism

  • Target Synonyms

    HGNC:12014; S adenosyl L methionine thiopurine S methyltransferase; Thiopurine methyltransferase; Thiopurine S methyltransferase; Thiopurine S-methyltransferase; TPMT; TPMT_HUMAN

  • Target Background

    This gene encodes the enzyme that metabolizes thiopurine drugs via S-adenosyl-L-methionine as the S-methyl donor and S-adenosyl-L-homocysteine as a byproduct. Thiopurine drugs such as 6-mercaptopurine are used as chemotherapeutic agents. Genetic polymorphisms that affect this enzymatic activity are correlated with variations in sensitivity and toxicity to such drugs within individuals, causing thiopurine S-methyltransferase deficiency. Related pseudogenes have been identified on chromosomes 3, 18 and X.

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