BeNa Culture Collection
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| 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 vial, dissolve completely, then Agar plate onto antibiotic plates (200 μL/Agar plate);④ Incubate the plates under specified conditions for 18–24 hours before observation (do not seal or wrap plates); ⑤ Pick a single colony and inoculate into 50 mL LB antibiotic-supplemented liquid medium; incubate overnight at 37°C on a shaking incubator; ⑥ Extract plasmid DNA from an appropriate volume of the culture as required by the experiment; |
| Growth conditions | 37°C; 18-24h; aerobic; |
| Storage conditions | -80°C |
| Safety level | 1 |
| Sharing mode | Public welfare sharing |