BeNa Culture Collection
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| Growth conditions | 37°C; 18-24h; aerobic |
| Subculture procedure | ① Prepare 1 vial of sterile water and 2 x 90mm resistant plates; ② Disinfect ampoule surface, open in biosafety cabinet, cauterize top with alcohol lamp, then immediately add sterile water to rupture; break ampoule with forceps; ③ Pipette 0.5 mL sterile water into lyophilized tube, dissolve completely, then spread solution onto antibiotic plates (200 μL/Agar plate); ④ Incubate the resistance plates under specified conditions for 18-24 hours before observation (do not seal or wrap plates); ⑤ Streak plates and pick single colonies onto 50mL LB resistance liquid medium; incubate overnight at 37°C on a shaking incubator; ⑥ Extract plasmids from an appropriate volume of bacterial culture as required by the experiment; |
| Storage conditions | 2-8°C |
| Sharing mode | Public welfare sharing |
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Human herpesvirus 2 nucleic acid reference (Heat inactivated) (Strongly positive)(Human herpesvirus 2 nucleic acid reference (Heat inactivated) (Strongly positive))
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Human herpesvirus 1 nucleic acid reference (Heat inactivated) (Strongly positive)(Human herpesvirus 1 nucleic acid reference (Heat inactivated) (Strongly positive))
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Dengue virus type 1 nucleic acid reference (Heat inactivated) (Strongly positive)(Dengue virus type 1 nucleic acid reference (Heat inactivated) (Strongly positive))
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Human adenovirus universal type DNA lab quality control(Human adenovirus universal type DNA lab quality control)
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Human adenovirus universal type DNA lab quality control(Human adenovirus universal type DNA lab quality control)
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