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- W2384515162 abstract "To establish a rapid diagnosis method for Babesia ovata,the PCR assay was developed with the specific primers were designed according to the sequence of the CCTη gene available in the GenBank.Under the optimized reaction conditions,the PCR assay was highly specific to amplify a 1,008 bp fragment from B.ovate genomic DNA with a detection limit of 34 copies,but no amplification with the DNA of B.bovis,B.bigemina and Theileria sergenti.Furthermore,a total of 49 blood DNA samples were tested by the PCR method and the results confirmed that the PCR method was sensitive and specific for detecting B.ovata infection in cattle." @default.
- W2384515162 created "2016-06-24" @default.
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- W2384515162 date "2012-01-01" @default.
- W2384515162 modified "2023-09-26" @default.
- W2384515162 title "Establishment of PCR assay for detection of Babesia ovata" @default.
- W2384515162 hasPublicationYear "2012" @default.
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