BeNa Culture Collection
info@bncc.com
| Culture medium | BNCC363359 |
| Description | VR-1740 Specific Medium |
| Composition | EMEM+1 μg/ mL TPCK- treated Trypsin |
| Growth conditions | 37°C; days; microaerophilic (3%-5% O₂, 10% CO₂); |
| Subculture procedure | ① Inoculation procedure: 24-48 hours before inoculation, transfer the frozen host cells into T25 flask, remove the cell culture medium when the host cell density reaches 80-90%, and inoculate 100-500 μL of virus solution. Adsorb under growth conditions for 1-2 hours, gently shake the T25 flask every 15-30 minutes to make the virus distribution more uniform; Add 6mL of virus growth medium to end adsorption, transfer to the incubator for further cultivation, and regularly observe the cytopathy; ② Virus collection: Once all host cells have developed lesions, virus liquid collection can begin. When collecting, the cells are repeatedly frozen and thawed 1-2 times, and then filtered through a 0.22 μ m pore size filter. The collected filtrate is the virus solution. |
| Storage conditions | liquid nitrogen |
| Sharing mode | Public welfare sharing |
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