BeNa Culture Collection
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| 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: Seed host cells into T25 flasks 24–48 hours prior to inoculation, and prepare for viral inoculation when the host cell density reaches 80–90%; Remove the cell culture medium and inoculate 100–500 μL of viral suspension. Allow adsorption for 1–2 hours under culture conditions, gently shaking the T25 flask every 15–30 minutes to ensure even viral distribution; add 6 mL of viral growth medium to complete adsorption, transfer to the incubator for continued culture, and monitor cytopathic effects periodically; ② Virus Harvesting: Once all host cells exhibit cytopathic effects, begin harvesting the viral supernatant. During harvesting, freeze-thaw the cells 1–2 times, then filter through a 0.22 μm pore size filter; the collected filtrate constitutes the viral supernatant. |
| 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