Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Complement System01:27

Complement System

The complement system is a group of approximately 20 plasma proteins that strengthen the body's defenses against infections through opsonization, inflammation, and cell lysis. Opsonization involves coating pathogens with complement proteins, making them more recognizable and facilitating phagocyte engulfment. Certain complement proteins induce inflammation that attracts immune cells to the site of infection. Cell lysis involves the destruction of pathogens through the formation of a membrane...
Enzyme-Linked Immunosorbent Assay01:33

Enzyme-Linked Immunosorbent Assay

In 1971, Peter Perlman and Eva Engvall developed an Enzyme-linked immunosorbent assay (ELISA or EIA). ELISA differs from western blot in that the assays are conducted in microtiter plates or in vivo rather than on an absorbent membrane.
There are many different types of ELISAs, but they all involve an antibody molecule whose constant region binds an enzyme, leaving the variable region free to bind its specific antigen.  Enzyme-substrate reaction allows the antigen to be visualized or quantified.

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

In vivo evidence of effective complement modulation by TriFu in comparison to C5 inhibition and complement depletion.

Blood advances·2026
Same author

The Interaction Between Mental Distress and Opioid Maintenance Treatment Impacts Levels of Circulating Cytokines.

Addiction biology·2026
Same author

Attenuating pulmonary injury and inflammation with C5/CD14 inhibition therapy: results from a porcine polytrauma model with blunt chest trauma.

European journal of trauma and emergency surgery : official publication of the European Trauma Society·2026
Same author

Combined inhibition of the complement component C5 and the TLR-coreceptor CD14 alters the posttraumatic response in fracture hematoma in a porcine polytrauma model.

Innovative surgical sciences·2026
Same author

Genetically predicted mannose-binding lectin levels and risk of future venous thromboembolism-the HUNT Study.

Journal of thrombosis and haemostasis : JTH·2026
Same author

Associations between systemic inflammation and cognitive trajectories post-stroke.

Scientific reports·2025
Same journal

Silicone oil in protein drug products and its implications for formulation stability.

Advanced drug delivery reviews·2026
Same journal

Targeted delivery of proteolysis-targeting chimeras (PROTAC) and molecular glue degraders (MGD).

Advanced drug delivery reviews·2026
Same journal

Lysosome-targeting degrader delivery system: from formulation design to biomedical applications.

Advanced drug delivery reviews·2026
Same journal

Anti-PEG antibodies in nanomedicine: Mechanisms, risks, and opportunities.

Advanced drug delivery reviews·2026
Same journal

Optimizing macrophage-targeted intracellular delivery systems for safe and effective immunotherapies.

Advanced drug delivery reviews·2026
Same journal

Light-controlled CRISPR-dCas9 epigenome editing: advanced drug-delivery strategies and oncology applications.

Advanced drug delivery reviews·2026
See all related articles

Related Experiment Video

Updated: Jun 1, 2026

Methods for Quantitative Detection of Antibody-induced Complement Activation on Red Blood Cells
06:29

Methods for Quantitative Detection of Antibody-induced Complement Activation on Red Blood Cells

Published on: January 29, 2014

Advances in assay of complement function and activation.

Morten Harboe1, Ebbe Billmann Thorgersen, Tom Eirik Mollnes

  • 1Institute of immunology, University of Oslo and Oslo University Hospital, Rikshospitalet, N-0027 Oslo, Norway.

Advanced Drug Delivery Reviews
|June 14, 2011
PubMed
Summary
This summary is machine-generated.

The complement system detects danger signals, like foreign materials. New methods using antibodies help measure complement activation, crucial for developing biocompatible materials.

More Related Videos

High-resolution Melting PCR for Complement Receptor 1 Length Polymorphism Genotyping: An Innovative Tool for Alzheimer's Disease Gene Susceptibility Assessment
07:26

High-resolution Melting PCR for Complement Receptor 1 Length Polymorphism Genotyping: An Innovative Tool for Alzheimer's Disease Gene Susceptibility Assessment

Published on: July 18, 2017

Measuring the 50% Haemolytic Complement (CH50) Activity of Serum
08:26

Measuring the 50% Haemolytic Complement (CH50) Activity of Serum

Published on: March 29, 2010

Related Experiment Videos

Last Updated: Jun 1, 2026

Methods for Quantitative Detection of Antibody-induced Complement Activation on Red Blood Cells
06:29

Methods for Quantitative Detection of Antibody-induced Complement Activation on Red Blood Cells

Published on: January 29, 2014

High-resolution Melting PCR for Complement Receptor 1 Length Polymorphism Genotyping: An Innovative Tool for Alzheimer's Disease Gene Susceptibility Assessment
07:26

High-resolution Melting PCR for Complement Receptor 1 Length Polymorphism Genotyping: An Innovative Tool for Alzheimer's Disease Gene Susceptibility Assessment

Published on: July 18, 2017

Measuring the 50% Haemolytic Complement (CH50) Activity of Serum
08:26

Measuring the 50% Haemolytic Complement (CH50) Activity of Serum

Published on: March 29, 2010

Area of Science:

  • Immunology and Materials Science
  • Complement system biology
  • Biomaterials and biocompatibility

Background:

  • The complement system's primary role is recognizing danger signals, including pathogen-associated molecular patterns and foreign surfaces.
  • Exposure to foreign surfaces, such as biomedical materials and nanoparticles, triggers an inflammatory response via complement activation.
  • Complement activation occurs when a surface is recognized as foreign, disrupting the balance of regulatory proteins like factor H and factor B.

Purpose of the Study:

  • To review available methods for studying complement activation on surfaces and in biological fluids.
  • To highlight the importance of sensitive detection methods for assessing biomaterial biocompatibility.
  • To inform the development of novel materials with improved biocompatibility through understanding complement interactions.

Main Methods:

  • Development of monoclonal antibodies targeting neoepitopes on complement activation products.
  • Assay development for sensitive detection of complement activation in fluid and on surfaces.
  • In vitro and in vivo studies of human and animal complement function and activation.

Main Results:

  • Monoclonal antibodies provide new, sensitive methods for quantifying complement activation.
  • Impaired regulation of complement control proteins (e.g., factor B and H balance) is key to surface-induced activation.
  • Sensitive detection assays are essential for evaluating the biocompatibility of artificial materials.

Conclusions:

  • Understanding complement activation mechanisms on foreign surfaces is critical for materials science.
  • Sensitive detection methods are prerequisites for developing biocompatible biomedical materials.
  • This review consolidates current methodologies for studying complement activation, aiding future research in biomaterial development.