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 Experiment Videos

Screening test for complement activation by counterimmunoelectrophoresis.

C M Arroyave, D G Taylor, P Gallup

    American Journal of Clinical Pathology
    |April 1, 1978
    PubMed
    Summary
    This summary is machine-generated.

    Related Concept Videos

    You might also read

    Related Articles

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

    Sort by
    Same author

    Tips and tricks for rectal dissection during laparoscopic ultra-low anterior resection.

    Techniques in coloproctology·2018
    Same author

    Developing and paying for medicines for orphan indications in oncology: utilitarian regulation vs equitable care?

    British journal of cancer·2012
    Same author

    The estimation of beef carcass muscle using cross-sectional area of M. longissimus dorsi at the fifth rib.

    Meat science·2011
    Same author

    Primal joints and hind-leg cuts of entire and castrated Javan rusa (Cervus timorensis russa) stags.

    Meat science·2011
    Same author

    Investigations into the accuracy of prediction of beef carcass composition using subcutaneous fat thickness and carcass weight I. Identifying problems.

    Meat science·2011
    Same author

    Investigations into the accuracy of prediction of beef carcass composition using subcutaneous fat thickness and carcass weight II. Improving the accuracy of prediction.

    Meat science·2011
    Same journal

    Communication patterns among surgical pathologists: a retrospective review of ideal strategies in a tertiary care setting.

    American journal of clinical pathology·2026
    Same journal

    Invasive urothelial carcinoma in association with surface low-grade papillary urothelial carcinoma: clinical and pathologic insights from a rare entity.

    American journal of clinical pathology·2026
    Same journal

    CEACAM1 expression by immunohistochemistry in B-cell lymphomas and plasma cell myeloma.

    American journal of clinical pathology·2026
    Same journal

    Comprehensive multicriteria life cycle assessment of biopsy processing in a surgical pathology department.

    American journal of clinical pathology·2026
    Same journal

    Prognostic significance of Myb protein and its downstream target genes in lacrimal gland adenoid cystic carcinoma.

    American journal of clinical pathology·2026
    Same journal

    Mismatch repair protein "nonclassic expression loss" pattern in colorectal cancer: an important staining pattern that is not well understood.

    American journal of clinical pathology·2026
    See all related articles

    Counterimmunoelectrophoresis (CIE) rapidly detects complement system activation via C3 split products. This sensitive method identifies complement activation in rheumatic diseases, even with normal C3 levels.

    Area of Science:

    • Immunology
    • Clinical Chemistry

    Background:

    • The complement system plays a crucial role in immune responses.
    • Activation of the complement system can lead to the formation of split products, such as C3c/d.
    • Detecting these split products indicates complement system activation, relevant in various diseases.

    Purpose of the Study:

    • To evaluate counterimmunoelectrophoresis (CIE) as a sensitive and rapid method for detecting complement system activation.
    • To assess the presence of C3 split products (C3c/d) in patients with systemic rheumatic diseases and healthy individuals.

    Main Methods:

    • Counterimmunoelectrophoresis (CIE) was employed to detect C3 split products (C3c/d) in plasma and serum samples.
    • Hemolytic assays (CH50, C4H50, C3H50) and radial immunodiffusion (RID) were used to measure complement component concentrations.

    Related Experiment Videos

  • Clinical investigation involved 40 patients with systemic rheumatic diseases and 116 healthy controls.
  • Main Results:

    • CIE detected C3 split products in 30% of serum samples from healthy individuals, compared to 2.5% in simultaneously collected plasma samples.
    • In patients with active systemic rheumatic diseases, C3 split products were identified by CIE in all but one case.
    • These findings were observed even when C3 protein levels, measured by RID, were normal.

    Conclusions:

    • CIE is a highly sensitive and rapid technique for detecting complement system activation through C3 split products.
    • The presence of C3 split products, detectable by CIE, is a significant indicator of complement activation in systemic rheumatic diseases.
    • CIE offers a valuable diagnostic tool for identifying complement activation when traditional methods show normal C3 protein levels.