Pseudo-Immunolabelling With the Avidin–Biotin–Peroxidase Complex due to the Presence of Endogenous Biotin in the Retina

2008 ◽  
pp. 129-138
Author(s):  
Willem Kamphuis ◽  
Jan Klooster
Keyword(s):  
2007 ◽  
Vol 131 (7) ◽  
pp. 1047-1055
Author(s):  
Sze Chuen Cesar Wong ◽  
John K. C. Chan ◽  
Elena S. F. Lo ◽  
Amanda K. C. Chan ◽  
Manson C. K. Wong ◽  
...  

Abstract Context.—In immunohistochemistry, nonstandardized antigen retrieval protocols and fluids, poor-quality antibodies, and the presence of endogenous biotin frequently lead to incorrect results. Recently, advanced reagents including bifunctional SkipDewax pretreatment solution (BSPS), rabbit monoclonal (RM) antibodies, and biotin-free polymer detection systems (PDSs) have been developed, which, it is claimed, resolve these problems. Objectives.—To determine whether BSPS, RM antibodies, and biotin-free PDSs improve the accuracy of immunohistochemistry; to optimize a new protocol consisting of a combination of BSPS, RM antibodies, and PDSs; and to compare it with a conventional protocol. Design.—The efficacies of BSPS, RM antibodies, and PDSs were compared with those of their respective conventional reagents using multitissue spring-roll sections. The new protocol was compared with a conventional protocol using Ki-67 immunostaining of 49 colorectal carcinoma specimens. Results.—For antigen retrieval, BSPS resulted in similar or better tissue staining than an EDTA solution, but the efficacy of BSPS decreased when it was reused. Most RM antibodies resulted in a greater proportion of positive cells than the corresponding non-RM antibodies, which did not produce satisfactory results in the absence of antigen retrieval. The PDSs Bond, ChemMate, and SuperPicture resulted in a high percentage of positive cells, good staining intensities, and low backgrounds. Other PDSs, except that from Ventana, resulted in high backgrounds and false positivity. The new combined protocol resulted in better Ki-67 staining than the conventional assay. Conclusions.—Bifunctional SkipDewax pretreatment solution, RM antibodies, and PDSs improve staining quality and diagnostic accuracy of immunohistochemistry assays and provide a foundation for standardization.


2005 ◽  
Vol 36 (2) ◽  
Author(s):  
Liliana Cruz Spano ◽  
Paulo Roberto Merçon de Vargas ◽  
José Paulo Gagliardi Leite ◽  
Jussara Pereira do Nascimento

2000 ◽  
Vol 23 (4) ◽  
pp. 327-331 ◽  
Author(s):  
Zuo-rong Shi ◽  
Alfred Au ◽  
Rosalia Soriano ◽  
Jian-xing Zhao ◽  
William L. Sweet

2016 ◽  
Author(s):  
Honoree Fleming

In 1998, we published a paper (Fleming et.al, 1998) describing some aspects of Ishikawa endometrial epithelial cell differentiation from monolayer cells into cells forming fluid-filled hemispheres called domes. The process begins with the dissolution of membranes within discrete regions of the monolayer. Nuclei from fused cells aggregate and endogenous biotin in particulate structures assumed to be mitochondria increase throughout the resulting syncytium. Endogenous biotin is also the distinguishing feature of a membrane that surrounds aggregates of multiple nuclei in a structure called a mitonucleon. The current paper includes additional observations on structural changes accompanying Ishikawa differentiation. Vacuoles form in the heterochromatin of the mitonucleon and within the biotin-containing double membrane surrounding heterochromatin. With the formation of vacuoles, the mitonucleon can be seen to rise along with the apical membrane of the syncytium in which it formed. The small vacuoles that form within the heterochromatin result in structures similar to “cells with optically clear nuclei” found in some cancers. The second larger vacuole that forms within the membrane surrounding the heterochromatin transforms the cell profile to one that resembles “signet ring” cells also observed in some cancers. Eventually the membrane surrounding the massed heterochromatin, generated three to four hours earlier, is breached and previously aggregated nuclei disaggregate. During this process heterochromatin in the mitonucleons undergoes changes usually ascribed to cells undergoing programmed cell death such as pyknosis and DNA fragmentation (Fleming, 2016b). The cells do not die, instead chromatin filaments appear to coalesce into a chromatin mass that gives rise to dome-filling nuclei by amitosis during the final three to four hours of the 20 hour differentiation (Fleming, 2016c).


2014 ◽  
Vol 406 ◽  
pp. 143-147 ◽  
Author(s):  
Raju Ahmed ◽  
Emma Spikings ◽  
Shaobo Zhou ◽  
Andrew Thompsett ◽  
Tiantian Zhang

2000 ◽  
Vol 29 (9) ◽  
pp. 445-451 ◽  
Author(s):  
Chang-Sheng Lu ◽  
Kenji Kashima ◽  
Tsutomu Daa ◽  
Shigeo Yokoyama ◽  
Shigetaka Yanagisawa ◽  
...  

1995 ◽  
Vol 16 (1) ◽  
pp. 38-46 ◽  
Author(s):  
M. RUSCKOWSKI ◽  
M. FOGARASI ◽  
F. VIRZI ◽  
D. J. HNATOWICH
Keyword(s):  

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