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Recombinant Human Alanine aminotransferase 2 (GPT2)

ACP14511

Number
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High Purity LevelsPrecision and ReliabilityCustomization Options

Specifications


Cat.No ACP14511 Target NameGPT2
FormLyophilized powderExpression SystemCustom Production. Please inquire and provide the desire expression system.
Expression Range1-523Protein LengthFull length protein
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 IDQ8TD30
Background Information
  • Uniprot Id

    Q8TD30

  • Target Species

    Human

  • Target Name

    GPT2

  • Target Full Name

    Alanine aminotransferase 2

  • Target Function

    Catalyzes the reversible transamination between alanine and 2-oxoglutarate to form pyruvate and glutamate.

  • Target Involvement

    Mental retardation, autosomal recessive 49 (MRT49)

  • Target Protein Families

    Class-I pyridoxal-phosphate-dependent aminotransferase family, Alanine aminotransferase subfamily

  • Target Tissue Specificity

    Expressed at high levels in muscle, adipose tissue, kidney and brain and at lower levels in the liver and breast.

  • Target Research Area

    Metabolism

  • Target Synonyms

    AAT2; Alanine aminotransferase 2; ALAT2_HUMAN; ALT2; Glutamate pyruvate transaminase 2; Glutamic alanine transaminase 2; Glutamic pyruvate transaminase (alanine aminotransferase) 2; Glutamic pyruvic transaminase 2; Glutamic--alanine transaminase 2; Glutamic--pyruvic transaminase 2; GPT 2; gpt2

  • Target Background

    This gene encodes a mitochondrial alanine transaminase, a pyridoxal enzyme that catalyzes the reversible transamination between alanine and 2-oxoglutarate to generate pyruvate and glutamate. Alanine transaminases play roles in gluconeogenesis and amino acid metabolism in many tissues including skeletal muscle, kidney, and liver. Activating transcription factor 4 upregulates this gene under metabolic stress conditions in hepatocyte cell lines. A loss of function mutation in this gene has been associated with developmental encephalopathy. Alternative splicing results in multiple transcript variants.

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