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    Improved detection of terminal transferase (TdT): The use of detergents on glutaraldehyde-fixed non-dehydrated cells prevents denaturation and diffusion artifacts.
        
        Leuk. Res. 10, 1041-1049 (1986)
    
    
    
				TdT as an intranuclear enzyme mainly of immature lymphoid cells is commonly determined immunologically using air-dried cell smears fixed with methanol. Both cell dehydration and alcohol fixation were found here to denature TdT and surface antigens. This could be prevented by using non-dehydrated cells bound electrostatically to poly-L-lysine-coated slides, fixed minimally with glutaraldehyde and rendered permeable to antibodies by the non-ionic detergent Brij 56. Crosslinking glutaraldehyde in addition prevented diffusion of TdT to extranuclear sites. By avoiding artifacts of denaturation and diffusion, a higher sensitivity in the detection of TdT was achieved despite considerably lower quantities of antibody.
			
			
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        Publikationstyp
        Artikel: Journalartikel
    
 
    
        Dokumenttyp
        Wissenschaftlicher Artikel
    
 
     
    
    
        Schlagwörter
        Detergents; glutaraldehyde; immunocytochemistry; methanol; polylysine; sensitivity; terminal transferase
    
 
     
    
    
        Sprache
        englisch
    
 
    
        Veröffentlichungsjahr
        1986
    
 
     
    
        HGF-Berichtsjahr
        0
    
 
    
    
        ISSN (print) / ISBN
        0145-2126
    
 
    
        e-ISSN
        1873-5835
    
 
     
     
     
	     
	 
	 
    
        Zeitschrift
        Leukemia Research
    
 
		
    
        Quellenangaben
        
	    Band: 10,  
	    Heft: 8,  
	    Seiten: 1041-1049 
	    
	    
	
    
 
  
         
        
            Verlag
            Elsevier
        
 
         
	
         
         
         
         
         
	
         
         
         
    
         
         
         
         
         
         
         
    
        Begutachtungsstatus
        Peer reviewed
    
 
    
        Institut(e)
        Institut für Immunologie
    
 
     
     
     
     
     	
    
        PubMed ID
        3091949
    
    
    
        Scopus ID
        0022871886
    
    
        Erfassungsdatum
        1986-12-31