Process for reproducing virus of large brill hemorrhagic septicaemia by large brill fin clone
A technology for hemorrhagic sepsis and turbot, which is applied in the directions of viruses/phages, biochemical equipment and methods, microorganisms, etc., can solve problems such as failure to retrieve the successful reproduction of turbot virus.
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[0008] As an example, the present invention provides detailed and specific preparation or propagation methods.
[0009] 1. Isolation and preparation of turbot hemorrhagic septicemia virus: 2 diseased fish with viral hemorrhagic leukemia collected from the turbot farm, cut off the viscera (liver, spleen and stomach, etc.) of the diseased fish with dissecting scissors ) about 20 grams, put it into a 50 ml glass homogenizer, add 20 ml of serum-free commercially available MEM culture medium, and perform homogenization treatment to break the cells. After the homogenate becomes a uniform paste, collect the homogenate and put it into In a 50 ml centrifuge tube, centrifuge at 15000 rpm for 90 minutes, collect the centrifuged supernatant, and filter it with a 0.45 μm microporous filter in a sterile room to remove bacteria and directly use it for cell inoculation; the excess should not be used immediately After the inoculated virus liquid is sealed, store it in a refrigerator at 4°C for...
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