Related Experiment Video
Updated: Jun 3, 2026

Capsular Serotyping of Streptococcus pneumoniae by Latex Agglutination
Published on: September 25, 2014
Basic problems of serological laboratory diagnosis
1Institue for Clinical Microbiology and Immunology, St. Gallen, Switzerland.
Abstract:
Serological testing and the use of immunochemical techniques are well established in the clinical laboratory and then uses are still rapidly increasing. Serological tests are applied for the diagnosis of infectious diseases, autoimmune disorders, allergies, and malignancies. Yet despite their widespread use, immunoassays are inflicted with a number of significant problems that lead to a substantial variation in reliability and accuracy of currently available tests. In the recent process of establishing procedures and criteria for quality assurance in the clinical laboratory an increased awareness of these problems has arisen among the clinical and reference laboratories as well as among the manufacturers of commercial test kits. The recognition of this situation prompted the US National Committee for Clinical Laboratory Standards (NCCLS) to create specific guidelines that address "the generrc problems of preparation and characterization of antigens and antibodies, testing using these reagents, and understanding the results" These guidelines are made public in the NCCLS document I/LA 18-A Specifications for Immunological Testing for Infectious Diseases; Approved Guideline, issued in December 1994 (1). References to this document will be made in this chapter where appropriate, and particularly, attempts will be made to adhere to the definitions of terms and procedures as they are laid down in the NCCLS consensus document.
Related Concept Videos
Methods of Classification and Identification
Enzyme-Linked Immunosorbent Assay
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.
Western Blotting
The technique begins with separating proteins from the sample using sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE), followed by protein transfer, immunoblotting, and finally, protein detection.

