THE ENVISION(TM)- A NEW IMMUNOHISTOCHEMICAL METHOD FOR DIAGNOSTICS AND RESEARCH - CRITICAL COMPARISON WITH THE APAAP, CHEMMATE(TM), CSA, LABC, AND SABC TECHNIQUES( SYSTEM )
E. Sabattini et al., THE ENVISION(TM)- A NEW IMMUNOHISTOCHEMICAL METHOD FOR DIAGNOSTICS AND RESEARCH - CRITICAL COMPARISON WITH THE APAAP, CHEMMATE(TM), CSA, LABC, AND SABC TECHNIQUES( SYSTEM ), Journal of Clinical Pathology, 51(7), 1998, pp. 506-511
Aim-To assess a newly developed immunohistochemical detection system,
the EnVision(TM)+. Methods-A large series of differently processed nor
mal and pathological samples and 53 relevant monoclonal antibodies wer
e chosen. A chessboard titration assay was used to compare the results
provided by the EnVision(TM)+ system with those of the APAAP, CSA, LS
AB, SABC, and ChemMate(TM) methods, when applied either manually or in
a TechMate 500 immunostainer. Results-With the vast majority of the a
ntibodies, EnVision(TM)+ allowed two- to fivefold higher dilutions tha
n the APAAP, LSAB, SABC, and ChemMate(TM) techniques, the staining int
ensity and percentage of expected positive cells being the same. With
some critical antibodies (such as the anti-CDS), it turned out to be s
uperior in that it achieved consistently reproducible results with dif
ferently fixed or overfixed samples. Only the CSA method, which includ
es tyramide based enhancement, allowed the same dilutions as the EnVis
ion(TM)+ system, and in one instance (with the anti-cyclin D1 antibody
) represented the gold standard. Conclusions-The EnVision(TM)+ is an e
asy to use system, which avoids the possibility of disturbing endogeno
us biotin and lowers the cost per test by increasing the dilutions of
the primary antibodies. Being a two step procedure, it reduces both th
e assay time and the workload.