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Recombinant Human Formimidoyltransferase-cyclodeaminase (FTCD)

ACP01737

Number
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Specifications


Cat.No ACP01737 Target NameFTCD
Target Synonyms(Formiminotransferase-cyclodeaminase)(FTCD)(LCHC1)FormLiquid or Lyophilized powder
Expression SystemBaculovirusExpression Range1-541aa
Mol Weight64.5 kDaProtein LengthFull length
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 IDO95954
Background Information
  • Uniprot Id

    O95954

  • Target Species

    Human

  • Target Name

    FTCD

  • Target Full Name

    Formimidoyltransferase-cyclodeaminase

  • Target Function

    Folate-dependent enzyme, that displays both transferase and deaminase activity. Serves to channel one-carbon units from formiminoglutamate to the folate pool.; Binds and promotes bundling of vimentin filaments originating from the Golgi.

  • Target Involvement

    Glutamate formiminotransferase deficiency (FIGLU-URIA)

  • Target Subcellular Location

    Cytoplasm, cytoskeleton, microtubule organizing center, centrosome, centriole. Golgi apparatus. Note=More abundantly located around the mother centriole.

  • Target Protein Families

    Cyclodeaminase/cyclohydrolase family; Formiminotransferase family

  • Target Research Area

    Others

  • Target Synonyms

    Formimidoyltetrahydrofolate cyclodeaminase; Formimidoyltransferase cyclodeaminase; Formiminotetrahydrofolate cyclodeaminase; Formiminotransferase cyclodeaminase; Formiminotransferase-cyclodeaminase; FTCD; FTCD_HUMAN; Glutamate formiminotransferase; Glutamate formyltransferase; LCHC 1; LCHC1

  • Target Background

    The protein encoded by this gene is a bifunctional enzyme that channels 1-carbon units from formiminoglutamate, a metabolite of the histidine degradation pathway, to the folate pool. Mutations in this gene are associated with glutamate formiminotransferase deficiency. Alternatively spliced transcript variants have been found for this gene.

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