A kind of duck astrovirus vaccine and preparation method thereof
An astrovirus and vaccine technology, applied in the directions of biochemical equipment and methods, viruses, vaccines, etc., can solve the problems of no disease, economic losses in the duck industry, etc., and achieve the effect of good immunity, easy concentration processing, and stable quality.
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Embodiment 1
[0025] Preparation:
[0026] (1) Digest and disperse BHK-21 cells with trypsin, add 5% newborn bovine serum in DMEM culture solution in a spinner bottle at 37°C, 5% CO 2 After culturing to a monolayer of cells, the original culture medium was discarded, and the cells were washed 3 times with serum-free DMEM medium for inoculation of duck astrovirus type Ⅰ and type Ⅲ.
[0027] (2) Virus inoculation and cultivation: respectively inoculate the duck astrovirus type Ⅰ and type Ⅲ viruses into the cells prepared in step ① according to the final volume of 1:100, and absorb the virus solution at 37°C for 30 minutes, discard the virus liquid, and DMEM medium containing 1% newborn bovine serum at 37°C, 5% CO 2 Culture until the cells are terminated when lesions appear.
[0028] (3) Virus collection, concentration and purification and determination of virus content: the collected cell virus liquid was repeatedly frozen and thawed twice at -20°C, centrifuged at 4°C and 5000rpm for 10min,...
Embodiment 2
[0032] Preparation:
[0033] (1) Digest and disperse the BHK-21 cells with trypsin, add 10% newborn calf serum to the DMEM culture solution in a microcarrier reactor at 37°C and 5% CO 2 After culturing to a monolayer of cells, the original culture medium was discarded, and the cells were washed 3 times with serum-free DMEM medium for inoculation of duck astrovirus type Ⅰ and type Ⅲ.
[0034] (2) Virus inoculation and cultivation: respectively inoculate the duck astrovirus type Ⅰ and type Ⅲ virus species into the cells prepared in step ① according to the final volume of 1:1000, and absorb the virus solution at 37°C for 60 minutes, discard the virus liquid, and 2% newborn bovine serum in DMEM at 37°C, 5% CO 2 Culture until the cells are terminated when lesions appear.
[0035] (3) Virus collection, concentration and purification: freeze-thaw the above-mentioned inoculated diseased cells, collect the supernatant after centrifugation to obtain the virus stock solution; concentra...
Embodiment 3
[0038] Preparation:
[0039] (1) Digest and disperse the BHK-21 cells with trypsin, add 7% newborn bovine serum to the DMEM culture solution in a microcarrier reactor at 37°C and 5% CO 2 After culturing to a single layer of cells, the original culture medium was discarded, and the cells were washed 3 times with serum-free DMEM medium containing 2mM glutamine for inoculation of duck astrovirus type Ⅰ and type Ⅲ.
[0040] (2) Virus inoculation and cultivation: respectively inoculate the duck astrovirus type Ⅰ and type Ⅲ viruses into the cells prepared in step ① according to the final volume of 1:500, and absorb the virus solution at 37°C for 45 minutes, then discard the virus solution in the 1.5% newborn bovine serum in DMEM at 37°C, 5% CO 2 Culture until the cells are terminated when lesions appear.
[0041] (3) Virus collection, concentration and purification: freeze-thaw the above-mentioned inoculated diseased cells, collect the supernatant after centrifugation to obtain th...
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