BeNa Culture Collection
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| Subculture procedure | ① Prepare one vial of sterile water and two 90mm resistant plates;② Disinfect the ampoule surface, open it in a biosafety cabinet, cauterize the top with an alcohol lamp, then immediately add sterile water to rupture it. Break the ampoule using forceps; ③ Pipette 0.5 mL sterile water into the lyophilized tube. After complete dissolution, spread the solution onto antibiotic plates at 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 Pick a single colony and inoculate into 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; |
| Growth conditions | 37°C; 18-24h; aerobic; |
| Storage conditions | -80°C |
| Safety level | 1 |
| Sharing mode | Public welfare sharing |