Title: 2016 ACVIM Forum Research Abstract Program Document date: 2016_5_31
ID: 2y1y8jpx_407
Snippet: In phase three of the testing methodology, clinical samples sent to the laboratory were typed for the DEA 5 antigen to establish an incidence rate. Over a period of two months, the laboratory used convenience sampling to test for the DEA 5 antigen. At the closing of phase three, a total of 777 random canine samples were tested, with a total of 63 canines testing positive for the DEA 5 antigen, resulting in an incidence rate of 8.1 %, consistent w.....
Document: In phase three of the testing methodology, clinical samples sent to the laboratory were typed for the DEA 5 antigen to establish an incidence rate. Over a period of two months, the laboratory used convenience sampling to test for the DEA 5 antigen. At the closing of phase three, a total of 777 random canine samples were tested, with a total of 63 canines testing positive for the DEA 5 antigen, resulting in an incidence rate of 8.1 %, consistent with previously known incidence rates. Therefore, at the conclusion of phase three, it was determined the novel antisera was valid for the detection of the DEA 5 antigen.
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