BeNa Culture Collection
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| Growth conditions | 37°C; 5% CO₂ + 95% air; |
| Subculture procedure | ① Remove cryovials from liquid nitrogen or -80°C freezer, place in PE gloves, and quickly immerse in 37°C water bath. Shake cryovials to accelerate thawing; aim for complete thawing within 1 minute. ② Add the suspension to 6-7 mL of complete medium and incubate in a culture incubator. ③ Monitor medium pH and cell density. When cell density exceeds 2 × 10⁶ cells/mL, perform passage or cryopreservation. |
| Storage conditions | Liquid nitrogen |
| Sharing mode | Public welfare sharing |
Human adenovirus 10 reference (Heat inactivated) (Strongly positive)(Human adenovirus 10 reference (Heat inactivated) (Strongly positive))
BNCC362991
Human herpesvirus 2 nucleic acid reference (Heat inactivated) (Strongly positive)(Human herpesvirus 2 nucleic acid reference (Heat inactivated) (Strongly positive))
BNCC379480
Human herpesvirus 1 nucleic acid reference (Heat inactivated) (Strongly positive)(Human herpesvirus 1 nucleic acid reference (Heat inactivated) (Strongly positive))
BNCC382714
Dengue virus type 1 nucleic acid reference (Heat inactivated) (Strongly positive)(Dengue virus type 1 nucleic acid reference (Heat inactivated) (Strongly positive))
BNCC393913
Human adenovirus universal type DNA lab quality control(Human adenovirus universal type DNA lab quality control)
BNCC393959
Human adenovirus universal type DNA lab quality control(Human adenovirus universal type DNA lab quality control)
BNCC393960
Pseudomonas brenneri DNA standard
BNCC393974
Mycobacterium tuberculosis H37Ra lab quality control
BNCC393904
Candida haemulonii DNA standard
BNCC393743
Genomic DNA from Escherichia coli
BNCC393715
pACYC-MS2-PML-S
BNCC393710
Quantitative strains of micrococcus luteus
BNCC393650
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