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Mitochondrial Damage Detection Service

Mitochondrial Damage Detection Service

Various pathogenic factors can result in structural and functional impairments within mitochondria. Precise detection and evaluation of mitochondrial damage are essential for the study and diagnosis of mitochondrial disorders. Protheragen offers an advanced technology platform for mitochondrial damage detection, enabling you to advance your project research.

Overview of Mitochondrial Damage

Mitochondrial damage primarily manifests as increased permeability of the outer mitochondrial membrane resulting in the release of substances from the intermembrane space into the cytoplasm, decreased mitochondrial membrane potential, degradation of cardiolipin on the inner mitochondrial membrane or exposure of 7A6 antigen on the mitochondria. Mitochondrial disease is closely linked to mitochondrial damage.

Applications of Mitochondrial Damage Detection Service

The applications of our mitochondrial damage detection service span a wide range of research areas.

  • Drug Discovery and Development
    Screening and validation of compounds targeting mitochondrial dysfunction for potential therapeutic interventions, including assessment of drug efficacy and toxicity in preclinical models.
  • Biomarker Identification
    Identification of novel biomarkers associated with mitochondrial damage for disease diagnosis, prognosis, and monitoring.
  • Disease Mechanism Studies
    Investigation of underlying mechanisms contributing to mitochondrial dysfunction in mitochondrial diseases.

Fig. 1 Model for the mitochondrial damage for apoptosis induction by various proapoptotic compounds (Zorov, D. B., et al., 2014)Fig.1 Model for the mitochondrial damage for apoptosis induction by various proapoptotic compounds (Zorov, D. B., et al., 2014)

Our Services

Protheragen consistently offers tailored services for the detection of mitochondrial damage, and our comprehensive research platform with advanced analysis capabilities is designed to fulfill all your research requirements.

Mitochondrial Oxidative Phosphorylation Analysis

Molecular Analysis Service

  • Next-generation sequencing (NGS) is used for the identification of mitochondrial DNA mutations and nuclear gene variants associated with mitochondrial disorders.
  • Quantitative PCR (qPCR) is employed to measure gene expression levels related to mitochondrial function.
  • Mitochondrial DNA copy number quantification is performed to assess mitochondrial biogenesis.

Mitochondrial Membrane Potential Analysis

Biochemical Profiling Service

  • Reactive oxygen species (ROS) detection assays to evaluate oxidative stress levels.
  • Enzyme activity assays are conducted to evaluate the function of key mitochondrial enzymes involved in oxidative phosphorylation and metabolic pathways.
  • Metabolomic profiling is carried out to characterize changes in metabolite levels associated with mitochondrial dysfunction.

Mitochondrial Membrane Potential Analysis

Imaging Service

  • Fluorescence microscopy for visualizing mitochondrial morphology and dynamics.
  • Magnetic resonance imaging (MRI) and spectroscopy (MRS) are utilized for non-invasive assessment of mitochondrial function and tissue integrity.
  • Positron emission tomography (PET) imaging with mitochondria-specific tracers allows visualization of in vivo mitochondrial activity.

Our Advantages

Professional Team

Professional Team

Advanced Technologies

Advanced Technologies

Customized Solutions

Customized Solutions

Competitive Pricing

Competitive Pricing

Protheragen' mitochondrial damage detection service offers a comprehensive range of assays and expertise to support research endeavors focused on understanding and addressing mitochondrial diseases. Should you have any inquiries or require further insights into our extensive range of services, please do not hesitate to contact us.

Reference

  1. Zorov, D. B.; et al. (2014). Mitochondrial reactive oxygen species (ROS) and ROS-induced ROS release. Physiological reviews, 94(3), 909–950. https://doi.org/10.1152/physrev.00026.2013

For research use only, not for clinical use.