BeNa Culture Collection
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| Growth conditions | 37°C; 5% CO₂ + 95% air; |
| Subculture procedure | ①Inoculation 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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Usutu virus nucleic acid reference (Heat inactivated) (Strongly positive)
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Mycoplasma bovis DNA lab quality control
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Staphylococcus haemolyticus nucleic acid reference (Heat inactivated) (Strongly positive)
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Acinetobacter junii nucleic acid reference(Heat inactivated) (Strongly positive)
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Pseudomonas aeruginosa Migula nucleic acid reference (Heat inactivated) (Strongly positive)
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