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Recombinant Human Alpha-aminoadipic semialdehyde synthase, mitochondrial (AASS), Truncated

ACP10827

Number
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High Purity LevelsPrecision and ReliabilityCustomization Options

Specifications


Cat.No ACP10827 Target NameAASS
Target SynonymsAASSAlpha-aminoadipic semialdehyde synthase; mitochondrial; LKR/SDH) [Includes: Lysine ketoglutarate reductase; LKR; LOR; EC 1.5.1.8); Saccharopine dehydrogenase; SDH; EC 1.5.1.9)]FormLyophilized powder
Expression SystemCustom Production. Please inquire and provide the desire expression system.Protein LengthPartial
Purity>85% (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 IDQ9UDR5
Background Information
  • Uniprot Id

    Q9UDR5

  • Target Species

    Human

  • Target Name

    AASS

  • Target Full Name

    Alpha-aminoadipic semialdehyde synthase, mitochondrial

  • Target Function

    Bifunctional enzyme that catalyzes the first two steps in lysine degradation. The N-terminal and the C-terminal contain lysine-ketoglutarate reductase and saccharopine dehydrogenase activity, respectively.

  • Target Involvement

    Hyperlysinemia, 1 (HYPLYS1); 2,4-dienoyl-CoA reductase deficiency (DECRD)

  • Target Subcellular Location

    Mitochondrion.

  • Target Protein Families

    AlaDH/PNT family; Saccharopine dehydrogenase family

  • Target Tissue Specificity

    Expressed in all 16 tissues examined with highest expression in the liver.

  • Target Synonyms

    AASSAlpha-aminoadipic semialdehyde synthase; mitochondrial; LKR/SDH) [Includes: Lysine ketoglutarate reductase; LKR; LOR; EC 1.5.1.8); Saccharopine dehydrogenase; SDH; EC 1.5.1.9)]

  • Target Background

    This gene encodes a bifunctional enzyme that catalyzes the first two steps in the mammalian lysine degradation pathway. The N-terminal and the C-terminal portions of this enzyme contain lysine-ketoglutarate reductase and saccharopine dehydrogenase activity, respectively, resulting in the conversion of lysine to alpha-aminoadipic semialdehyde. Mutations in this gene are associated with familial hyperlysinemia.

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