peer reviewedSensitivity, specificity and predictive values of an enzyme-linked immunosorbent assay (ELISA) for detecting antibodies against bovine leukaemia virus (BLV) were evaluated using a representative sample of 145 serum pools, comprising from 3 to 48 individual sera. The sample was constituted according to the frequency distribution of the negative and positive pools analysed during a screening involving the whole cattle population of Belgium. Sensitivity and specificity were estimated to 88.9% and 100% and the predicted negative and positive values were 99.9% and 100%, respectively. These results indicate the use of serum pools is suitable for the detection of BLV infected herds in eradication campaigns
Enzyme-linked immunosorbent assay (ELISA) is often used to test bovineleukemia virus (BLV) infection...
Bovine Leukemia Virus (BLV) is a retrovirus that causes bovine enzootic leukemia (EBL). The routine ...
This study was carried out in order to serologically and haematologically determine the prevalance o...
<p>Sensitivity, specificity and predictive values of an enzyme-linked immunosorbent assay (ELI...
Serum, milk and urine specimens were taken from 15 bovine leukaemia virus (BLV)-positive and 20 BLV-...
The objective of this study was to validate a new blocking enzyme-linked immunosorbent assay (ELISA)...
Bovine Leukemia Virus (BLV) is the etiologic agent of Enzootic Bovine Leukosis, a retrovirus exogeno...
The incidence of antibodies to bovine leukemia virus in sera of cattle from Oklahoma was determined ...
An enzyme‐linked immunosorbent assay (ELISA) involving a monoclonal antibody was used to perform a l...
This study assessed the diagnostic performance of a commercial ELISA for detecting bovine leukemia v...
We developed an indirect ELISA test (rp24-ELISA) for the detection of antibodies against the p24 cap...
Sera collected from cattle with enzootic bovine lymphoma (EBL) were compared to sera from clinically...
A competition ELISA technique involving two monoclonal anti-gp51 antibodies has been developed for t...
I evaluated an enzyme-linked immunosorbent assay (ELISA) and agar gel immunodiffusion (AGID) test si...
A variant of the ELISA technique, involving a monoclonal anti-gp51 antibody yields a highly sesnsiti...
Enzyme-linked immunosorbent assay (ELISA) is often used to test bovineleukemia virus (BLV) infection...
Bovine Leukemia Virus (BLV) is a retrovirus that causes bovine enzootic leukemia (EBL). The routine ...
This study was carried out in order to serologically and haematologically determine the prevalance o...
<p>Sensitivity, specificity and predictive values of an enzyme-linked immunosorbent assay (ELI...
Serum, milk and urine specimens were taken from 15 bovine leukaemia virus (BLV)-positive and 20 BLV-...
The objective of this study was to validate a new blocking enzyme-linked immunosorbent assay (ELISA)...
Bovine Leukemia Virus (BLV) is the etiologic agent of Enzootic Bovine Leukosis, a retrovirus exogeno...
The incidence of antibodies to bovine leukemia virus in sera of cattle from Oklahoma was determined ...
An enzyme‐linked immunosorbent assay (ELISA) involving a monoclonal antibody was used to perform a l...
This study assessed the diagnostic performance of a commercial ELISA for detecting bovine leukemia v...
We developed an indirect ELISA test (rp24-ELISA) for the detection of antibodies against the p24 cap...
Sera collected from cattle with enzootic bovine lymphoma (EBL) were compared to sera from clinically...
A competition ELISA technique involving two monoclonal anti-gp51 antibodies has been developed for t...
I evaluated an enzyme-linked immunosorbent assay (ELISA) and agar gel immunodiffusion (AGID) test si...
A variant of the ELISA technique, involving a monoclonal anti-gp51 antibody yields a highly sesnsiti...
Enzyme-linked immunosorbent assay (ELISA) is often used to test bovineleukemia virus (BLV) infection...
Bovine Leukemia Virus (BLV) is a retrovirus that causes bovine enzootic leukemia (EBL). The routine ...
This study was carried out in order to serologically and haematologically determine the prevalance o...