BeNa Culture Collection
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| Growth conditions | 37 ℃; 18-24 hours; aerobic; |
| Subculture procedure | ① Prepare 1 sterile water tube and 2 90mm resistant plates; ② After disinfecting the surface of the ampoule tube, open it in a safety cabinet, burn the top with an alcohol lamp, quickly drip sterile water to break it, and then use tweezers to crush it; ③ Draw 0.5mL of sterile water and transfer it into a freeze-drying tube. After sufficient dissolution, apply the solution onto resistant plates at a rate of 200 μ L per Agar plate; ④ Place the resistant Agar plate under the specified conditions for cultivation for 18-24 hours and observe it (sealing and wrapping the Agar plate is prohibited); ⑤ Select a single colony and inoculate it into 50mL of liquid LB resistant medium. Incubate overnight at 37 ℃ on a shaker; ⑥ According to experimental requirements, extract an appropriate amount of bacterial solution for plasmid extraction; |
| Storage conditions | -80 ℃ |
| Sharing mode | Public welfare sharing |
Plasmid DNA of Infectious Hypodermal and Hematopoietic Necrosis Virus(Plasmid DNA of Infectious Hypodermal and Hematopoietic Necrosis Virus)
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Plasmid DNA of Peach Leaf Curl Virus (TSV)(Plasmid DNA of Peach Leaf Curl Virus (TSV))
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Plasmid DNA of Prawn yellow head virus(Plasmid DNA of Prawn yellow head virus)
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Rotavirus A nucleic acid reference (Heat inactivated) (Strongly positive)(Rotavirus A nucleic acid reference (Heat inactivated) (Strongly positive))
BNCC396427
Rotavirus A nucleic acid reference (Heat inactivated) (Strongly positive)(Rotavirus A nucleic acid reference (Heat inactivated) (Strongly positive))
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Human rhinovirus 53 nucleic acid reference (Heat inactivated) (Strongly positive)(Human rhinovirus 53 nucleic acid reference (Heat inactivated) (Strongly positive))
BNCC398205