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Detection of Babesia bigemina-infected carriers by polymerase chain reaction amplification.

A SpeI-AvaI fragment (0.3 kbp) from pBbi16 (a pBR322 derivative containing a 6.3-kbp Babesia bigemina DNA insert) was subcloned into the pBluescript phagemid vector and was sequenced by the dideoxy-mediated chain termination method. Two sets of primers were designed for the polymerase chain reaction...

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Bibliografische gegevens
Hoofdauteurs: Figueroa, J V, Chieves, L P, Johnson, G S, Buening, G M
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: 1992
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Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC270481/
https://ncbi.nlm.nih.gov/pubmed/1400956
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