TL;DR: A solid-phase enzyme-linked immunosorbent assay (ELISPOT) is described, which provides a useful alternative to conventional plaque-forming cell assays.
TL;DR: An immunoenzyme procedure is described for detection of proteins separated by SDS-polyacrylamide gel electrophoresis that can detect protein antigens at concentrations down to 0.5 ng/mm2.
TL;DR: The immunoenzyme procedure was found to give good correlation with the conventional cultural procedure and its sensitivity was comparable to that of the fluorescent antibody technique.
Abstract: An immunoenzyme conjugate was prepared by labeling the immunoglobulin G fraction of Salmonella polyvalent flagella1 anti-serum with horseradish peroxidase. The immunoenzyme conjugate, when reacted with pure cultures of bacteria and stained with 3–3′diaminobenzidine was found to specifically stain the cell wall and flagellae of salmonellae. Cells of salmonellae were stained brown after the immunoenzyme reaction and could be differentiated from unstained organisms under a light microscope at 1000X magnification. The immunoenzyme technique was applied to the rapid detection of salmonellae in meats and poultry products and the specificity and sensitivity of the method was donipared to that of the fluorescent antibody technique and conventional cultural technique. The immunoenzyme procedure was found to give good correlation with the conventional cultural procedure. Its sensitivity was comparable to that of the fluorescent antibody technique.
TL;DR: A recently described solid phase immunoenzyme procedure (ELISPOT) has been adapted for the detection of individual cells secreting fibronectin and should find useful application for studying fibronECTin production at the cellular level.
Abstract: A recently described solid phase immunoenzyme procedure (ELISPOT) has been adapted for the detection of individual cells secreting fibronectin Simple and sensitive, this technique should find useful application for studying fibronectin production at the cellular level