Abstract
Incorporation of trypsin and diethylaminoethyl-dextran in the overlay was found to be necessary for infectivity assay of the UK strain of bovine rotavirus by plaque assays. Small plaques of about 1 mm in radius were formed in BGM cells. Large plaques of about 3–4 mm in radius were consistently produced in monolayers of secondary calf kidney cultures.
Key words: bovine rotavirus, plaque assay, trypsin, diethyl-aminoethy1-dextran
Sammendrag
Ved at lade trypsin og diethylaminoethyl-dextran indgå i det faste substrat var det muligt at påvise bovin rotavirus (UK stammen) gennem plaque teknik. I kulturer af abeceller (BGM celler) blev der op-nået 1 mm store plaques, mens der i sekundaere kulturer af kalvenyre-celler regelmaessigt sås plaque af 3—4 mm st0rrelse.
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