Creative Biolabs offers high-quality cell-based complement activity assays to help your research and drug development projects. Our services represent a comprehensive solution for researchers seeking to understand and manipulate the complex dynamics of the complement system.
The complement system is an integral part of the immunity response and plays a vital role in defense against pathogens and immune regulation. Cell-based complement activity assays enable the direct assessment of complement activation and its consequences on target cells, mimicking in vivo conditions more closely than traditional biochemical assays. Therefore, cell-based complement activity assays have gradually emerged as a powerful tool to study the complex interactions between complement components and their target cells, providing insights into physiological and pathological processes.
Fig. 1 Complement activation pathways.1,3
At Creative Biolabs, we provide seamless end-to-end cell-based complement activity assay services from assay design to data analysis. Our experienced scientists rely on advanced methods and well-established procedures to ensure your complement activity assay project runs smoothly.
The cell-based complement activity assay, specifically the IFA assay, is a powerful and versatile technique utilized in immunology and biomedical research to evaluate the functional activity of the complement system. Following are simple protocols of the IFA assay.
Cell-ELISA is a sophisticated technique employed in biomedical research and diagnostics to evaluate the activation and functionality of the complement system within a cellular context. This assay marries the principles of traditional ELISA with the unique ability to monitor complement-mediated events directly on or near cell surfaces, providing a more physiologically relevant assessment compared to assays performed in solution.
Disease Pathogenesis
Illuminated the role of complement in autoimmune diseases, infectious diseases, and inflammatory conditions.
Therapeutic Development
Evaluating the efficacy of complement inhibitors or activators in modulating cellular responses, support the discovery and development of novel therapeutic strategies.
Drug Safety Testing
Assessing the potential for drugs to activate or inhibit the complement system is crucial for predicting adverse immune reactions and optimizing drug safety profiles.
Our team of highly skilled scientists boasts extensive experience in immunology and cell-based assays, ensuring the highest quality results.
We tailor our protocols to your specific research needs, adjusting antibody concentrations, and incubation times, or even incorporating additional controls as required.
Every step is rigorously validated using industry-standard practices, ensuring reproducibility and reliability of your data.
Detailed experimental reports, including raw data, analysis, and interpretation, are provided to empower your research insights.
Fig.2 Osteosarcoma cell-based complement system activitation.2,3
Recent research indicates that complement system activation plays a crucial role in tumor progression. Human bone osteosarcoma epithelial cells (U2-OS) have been shown to trigger the alternative complement pathway when exposed to pooled normal human serum. A cell-based ELISA method was developed to measure complement activation on the surface of eukaryotic cells. Verification of complement system activation by U2-OS cells involved analyzing MAC and C3b deposition using immunofluorescence and flow cytometry. PCR tests confirmed the absence of mycoplasma contamination. Post-complement activation, cell viability assessments revealed U2-OS cells as potential models for studying complement activation with sublytic MAC levels. MAC deposition on osteosarcoma tissues corroborates complement activation in these cancers. Tissue microarray experiments demonstrated evident MAC staining on tumor cells, suggesting that targeting the complement system could be a promising therapeutic strategy for cancer.
Contact us today to advance your complement research endeavors.
References