BeNa Culture Collection
info@bncc.com
| Culture medium | BNCC361988 |
| Description | EMEM Complete Medium (with 2% FBS) |
| Composition | 98% EMEM+2% FBS |
| Growth conditions | 37°C; 5% CO₂ + 95% air; |
| Subculture procedure | ① Inoculation procedure: 24-48 hours prior to inoculation, seed host cells in T25 flasks. Prepare for viral inoculation when host cell density reaches 80-90%; Remove the cell culture medium and inoculate 100-500μL of virus solution. Allow adsorption for 1-2 hours under culture conditions, gently shaking the T25 flask every 15-30 minutes to ensure even virus distribution. Add 6mL of virus growth medium to complete adsorption, then transfer to the incubator for continued culture. Regularly observe for cytopathic effects; ② Virus Harvesting: Initiate virus collection once host cells exhibit complete cytopathic changes. During collection, freeze-thaw the cells 1–2 times, then filter through a 0.22μm pore size filter. The collected filtrate constitutes the virus solution. |
| Storage conditions | Liquid nitrogen |
| Sharing mode | Public welfare sharing |
Quantitative strains of Bacillus subtilis subsp(Quantitative strains of Bacillus subtilis subsp)
BNCC367736
Influenza A virus(H3N2) nucleic acid reference (Heat inactivated) (Strongly positive)(Influenza A virus(H3N2) nucleic acid reference (Heat inactivated) (Strongly positive))
BNCC381677
Japanese encephalitis virus antigen test reference (Chemical inactivation) (Strongly positive)(Japanese encephalitis virus antigen test reference (Chemical inactivation) (Strongly positive))
BNCC394528
Human herpesvirus 3 DNA lab quality control(varicella-zoster virus)(Human herpesvirus 3 DNA lab quality control(varicella-zoster virus))
BNCC395778
JC polyomavirus DNA lab quality control(JC polyomavirus DNA lab quality control)
BNCC394335
Canine parainfluenza virus nucleic acid reference (Heat inactivated) (Strongly positive)(Canine parainfluenza virus nucleic acid reference (Heat inactivated) (Strongly positive))
BNCC393916