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Neospora응집반응을 이용한 네오스포라증의 혈청학적 진단
강민수,김재훈,황우석,남호우,윤희정,배종희,김대용,Kang, Min-Soo,Kim, Jae-Hoon,Hwang, Woo-Suk,Nam, Ho-Woo,Youn, Hee-Jeong,Bae, Jong-Hee,Kim, Dae-Yong 대한수의학회 2003 大韓獸醫學會誌 Vol.43 No.4
Currently, both the indirect fluorescent antibody test (IFAT) and enzyme linked immunosorbent assay (ELISA) have been used to detect Neospora caninum antibodies. Several factors such as the buffers, the conjugate, the pattern of fluorescence, and the cross reactivity with other apicornplexan protozoan, may result in poorly correlated data. The present study was undertaken to develop and evaluate the Neospora agglutination test (NAT) for the detection and quantification of IgG antibodies to N. caninum from various animal species. Compared to the ELISA method, the NAT with a cutoff value of 1:512 gave a high index of coincidence (kappa=0.807) and no cross reactivity to Toxoplasma gondii antiserum. Hence, this NAT method, which did not require a species-specific secondary antibody and expensive tools, would be easily available for the detection of antibodies to N. caninllm of various animal species.