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    Kynurenine Analysis Service

      The kynurenine pathway is the primary route for the catabolism of the amino acid tryptophan in mammals, leading to the production of several biologically active metabolites. The process begins with the oxidation of tryptophan by either tryptophan dioxygenase (TDO), primarily in the liver, or indoleamine dioxygenase (IDO) in peripheral tissues, producing N-formylkynurenine. This intermediate is then converted into kynurenine by formamidase.

       

      Kynurenine serves as a key branching point in the pathway, leading to the production of several downstream metabolites. Kynurenine 3-monooxygenase (KMO) converts kynurenine into 3-hydroxykynurenine (3-HK), which is further metabolized by kynureninase to produce 3-hydroxyanthranilic acid (3-HAA). From 3-HAA, quinolinic acid, a neurotoxic metabolite, is formed, which is a precursor for nicotinamide adenine dinucleotide (NAD+) synthesis. Alternatively, kynurenine can be converted into kynurenic acid (KYNA) by kynurenine aminotransferases (KATs). 

       

      Kynurenic acid acts as a neuroprotective agent by antagonizing excitatory NMDA receptors and blocking alpha-7 nicotinic acetylcholine receptors. The balance between kynurenic acid (neuroprotective) and quinolinic acid (neurotoxic) is critical in regulating neuroinflammation and neurodegeneration. Dysregulation of this pathway has been linked to several diseases, including Alzheimer's disease, Parkinson's disease, and major depressive disorder. The pathway's metabolites also play significant roles in immune modulation, influencing T-cell activity and immune responses.

       

      1831609406069526528-SchematicDiagramofTheKynureninePathway.png

       

      Chatterjee, P. et al. Sci Rep. 2018.

       

      Figure 1. Schematic Diagram of The Kynurenine Pathway

       

      Accurate quantification of kynurenine and its metabolites is essential for advancing research into these complex metabolic networks and their implications in disease. At MtoZ Biolabs, our Kynurenine Analysis Service utilizes state-of-the-art mass spectrometry (MS) techniques, ensuring high sensitivity and specificity for detecting kynurenine and its pathway metabolites across various biological samples, offering critical insights for biomedical research and clinical applications.

       

      Analysis Workflow

       

      1831603845470998528-WorkflowforKynurenineAnalysisService.png

       

      Service Advantages

      • Highly Efficient Sample Recovery and Processing
      • Accurate and Reliable Detection and Quantification
      • Capability to Handle Various Sample Types
      • Customized Data Analysis Services
      • Rapid Service Response and Cost-Effectiveness

       

      Applications

      Kynurenine analysis is essential in numerous fields of study, including neuroscience, immunology, oncology and psychiatry.

       

      Sample Submission Requirements

      1. Sample Types

      Serum, plasma, urine, tissues and other biological samples. For each sample, more than 3 materials of the same condition must be selected.

       

      2. Sample Volume

      • Animal tissue ≥ 100 mg
      • Plant tissue ≥ 200 mg
      • Serum/ Plasma ≥ 200 μL
      • Urine ≥ 2 mL

       

      3. Sample Preservation

      Samples should be stored at -80°C to maintain stability.

       

      Note: Please provide details on sample collection and handling.

       

      Deliverables

      1. Experimental Procedures

      2. Relevant Liquid Chromatography and Mass Spectrometry Parameters

      3. Detailed Information on Kynurenine

      4. Raw Data

      5. Custom Analysis Report

       

      Contact us today to learn how our Kynurenine Analysis Service can support your research. At MtoZ Biolabs, we are committed to accelerating your scientific discoveries.

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