Improvement of Protocol for EB Virus-Detecting in Situ Hybridization Using FITC-Labeled PNA Probe and its Application to Pathological Diagnosis
	    		
	    			
	    			
		        		
			        		
		        		
			        
		   		
		   		
		   			
		   		
	    	
    	 
    	10.2185/jjrm.64.882
   		
        
        	
        		- VernacularTitle:EBER PNAプローブを用いたEBウイルス検出方法の利便性の向上と診断への応用について
 
        	
        	
        	
        		- Author:
	        		
		        		
		        		
			        		Mari WAKAMATSU
			        		
			        		;
		        		
		        		
		        		
			        		Naoyuki SUMIYOSHI
			        		
			        		;
		        		
		        		
		        		
			        		Tomohiko YOKOI
			        		
			        		;
		        		
		        		
		        		
			        		Miho SENDA
			        		
			        		;
		        		
		        		
		        		
			        		Maki FUNABASHI
			        		
			        		;
		        		
		        		
		        		
			        		Ryuichi FUKUYAMA
			        		
			        		
		        		
		        		
		        		
		        		
		        		
			        		
			        		
		        		
	        		
        		 
        	
        	
        	
        		- Publication Type:Journal Article
 
        	
        	
            
            
            	- From:Journal of the Japanese Association of Rural Medicine
	            		
	            		 2016;64(5):882-885
	            	
            	
 
            
            
            	- CountryJapan
 
            
            
            	- Language:Japanese
 
            
            
            	- 
		        	Abstract:
			       	
			       		
				        
				        	  We made some improvements on the in situ hybridization protocol for EB virus (EBV) detection so that many general laboratories in Japan are able to perform the procedure. Using FITC-labeled EBER-PNA probes (DAKO), we examined dilutions of several chemicals and the incubation temperature of the probes in tissue sections. We confirmed the accuracy and reproducibility of our protocol by applying PCR to detect EBV genomes within tissue sections. We applied the technique to 55 laboratory samples which were suspected to be infected with EBV, and eight negative control and successfully ended up with pathological diagnosis. Moreover, coupled with immunohistochemical detection of LMP-1, we could determine the type of EBV infection.