The complement system is a complex immunoregulatory network composed of more than 30 proteins, and abnormal activity of its components is closely associated with infections, autoimmune diseases, genetic defects and other diseases. The assay of individual components focuses on the mechanism of action and biological function of specific complement proteins in the cascade reaction, providing key data for the study of complement regulatory mechanisms and disease associations. Individual complement component activity assay is used to quantitatively or qualitatively analyze the functional activity or content of a specific component of the complement system (e.g., C3, C5, C1q, Factor B, etc.).
Whether you are in mechanism discovery, drug development, or preclinical evaluation, we can provide reliable, customized activity testing solutions for individual complement components for your research.
Compatible with a wide range of sample types
Highly specific assay platform for precise assessment
Combining sensitivity and quantification
Flexible adjustment of experimental procedures and assay indexes
We have briefly summarized the workflow for testing several complement components. For more information or customized service solutions, please feel free to contact us.
Sandwich ELISA: For C1q binding analysis
For C1q binding analysis, plates were coated with PAT-SM6 or controls (isotype or Rituximab). After blocking, plates were incubated with human C1q followed by sheep anti human C1q-HRP. PAT-SM6 showed clear but moderate binding to C1q compared to the isotype control. Rituximab displayed a stronger C1q binding capacity. PAT-SM6 mediated deposition of C1q on the surface of OPM-2 cells was assessed by using human C1q and detecting antibodies in FACS.
ELISA: For measurement of C3, C3a, Factor Ba, C5a, and sC5b-9 in sera
Serum was analyzed for C3, C3a, factor Ba, C5a, and sC5b-9 using an ELISA. Complement activation was shown to continue at early levels by tracking the levels of the central complement component C3. Depletion of C3 coupled with elevated levels of C3a, Ba, C5a, and sC5b-9 indicated that complement was activated and that activation proceeded to the level of the C3-converting enzymes and C5-converting enzymes and into the terminal pathway. The activation proceeds to the C3- and C5-converting enzyme levels and enters the terminal pathway.
References
Our testing services cover key components of the three complement activation pathways, classical, alternative and lectin, including but not limited to C1q, C3, C3a, C5, C5a, C9, Factor B, Factor D, MBL, Properdin, and various types of regulatory proteins such as Factor H, I and others. Customers can customize specific assay combinations according to their research objectives, and we can also provide standard panel recommendations for reference.
Yes, we support samples of human origin and a variety of animal model (e.g., mouse, rat, guinea pig, primate) sources. Common sample types include serum, plasma, cell supernatant, tissue homogenate, etc. Detailed guidelines for sample collection and preservation will be provided. We can also provide standardized sampling tubes and cold chain transport solutions to ensure sample quality.
Absolutely. We support group testing of bulk samples and comparative analysis of experimental conditions, and we can develop a multi-group parallel test plan according to your experimental design. At the same time, we provide data standardization and statistical analysis services to assist you in determining whether the changes in complement function under different conditions are statistically significant. This type of service is particularly suitable for drug efficacy evaluation, immune function monitoring or disease modeling studies.
Yes, we provide a full range of complement system research services, including:
We also support conjugation services, a one-stop solution for all your needs in complement research.
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