Hybridization of Horseradish Peroxidase-Labeled Probes and Detection by Enhanced Chemiluminescence

Author(s):  
Timothy Stone ◽  
Ian Durrant
1989 ◽  
Vol 22 (8) ◽  
pp. 1841-1859 ◽  
Author(s):  
A. P. Osipov ◽  
A. A. Arefyev ◽  
S. B. Vlasenko ◽  
E. M. Gavrilova ◽  
A. M. Yegorov

1990 ◽  
Vol 38 (3) ◽  
pp. 415-419 ◽  
Author(s):  
E Hawkins ◽  
R Cumming

The ability to use enhanced chemiluminescence (ECL) to detect horseradish peroxidase as a label for tissue antigens and cellular viral DNA was demonstrated. A liquid nitrogen-cooled charged-coupled device (CCD) was used to detect light output, which was visualized on a monitor or was quantitated using an attached microcomputer. In a tissue antigen model, equivalent sensitivity was observed between ECL and colorimetric detection.


Author(s):  
G M Sankolli ◽  
Raw Stott ◽  
G H G Thorpe ◽  
D Smith ◽  
B T Rudd ◽  
...  

Oestradiol in serum was determined with a simple enhanced chemiluminescent enzyme immunoassay. The assay is based on oestradiol labelled with horseradish peroxidase and the IgG fraction of an oestradiol antiserum coated on a black polystyrene microtitre plate. The enzyme activity of bound label was determined using a p-hydroxycinnamic acid-enhanced chemiluminescent reaction. The assay was sensitive (1·8 fmol/well), precise (intra- and inter-assay CV 4–10% and 8–12%, respectively for sample concentration in the range 122–1330 pmol/L) and showed good agreement with conventional radioimmunoassays ( r=0·99).


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