BeNa Culture Collection
info@bncc.com
| Growth conditions | 37 ℃; 7 days; 5% CO2+95% air; |
| Subculture procedure | ① Inoculation steps: 24-48 hours before inoculation, lay T25 bottles of host cells and prepare for virus inoculation when the host cell density reaches 80-90%; Remove the cell culture medium and inoculate 100-500 μ L of virus solution, adsorb under culture conditions for 1-2 hours, gently shake the T25 bottle 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 cell pathology; 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. The host cells are seeded in a 96 well plate and prepared for virus inoculation when the host cell density reaches 80-90%. ② Dilute the virus solution with complete culture medium in a 10 fold series, take 8 gradients of 10 ^ 1-10 ^ 8, and inoculate 100 μ L per well quantitatively. Inoculate 6 wells at each dilution and culture according to the culture conditions. Regularly observe and record the pathological changes of cells at each dilution |
| Storage conditions | liquid nitrogen |
| Sharing mode | Public welfare sharing |
Quantitative strains of bacillus cereus(Quantitative strains of bacillus cereus)
BNCC399551
Quantitative strains of Clostridium perfringens(Quantitative strains of Clostridium perfringens)
BNCC399657
KG-1a(KG-1a)
BNCC100983
SNU-5(SNU-5)
BNCC344674
Biochemical Identification Kit for Plesiomonas shigelloides(Biochemical Identification Kit for Plesiomonas shigelloides)
BNCC390163
Biochemical Identification Kit for Alcaligenes faecalis(Biochemical Identification Kit for Alcaligenes faecalis)
BNCC390167