BeNa Culture Collection
info@bncc.com
| Subculture procedure | ① Prepare 1-2 of the above plates; ② Open the safety cabinet and follow the arrow indication on the cap of the penicillin bottle to open the strain and reconstitution solution; ③ Add 1mL of the complex solution to the Freeze dried pellet, cover with a rubber stopper, and shake to dissolve; ④ Take 200 μ L of bacterial suspension separately and inject it into two plates, apply evenly; ⑤ Place the petri dish under the above cultivation conditions for cultivation, and once the bacterial strain grows, it can be used. |
| Growth conditions | 37 ℃, 18-24h, aerobic |
| Storage conditions | 2-8 ℃ |
| Safety level | 2 |
| morphology | The colony diameter is 0.5-1mm, circular, with neat edges, opaque, gray white on the front, raised in the middle, smooth and bright on the surface, moist texture, easy to pick up, G - (red), Bacillus, purity: pure |
| Sharing mode | Public welfare sharing |
Acinetobacter baumannii
Storage conditions: 2~8 ℃
No. 254392
Product format: freeze dried,200ul
Validity period: 6 years
Biosafety level: 2, handle in safety cabinet
Receving notice: if any abnormality is found on the day of receipt, please contact the customer service within 24 hours. If it is overdue, it is deemed that the bacteria are well. The freeze dried culture shall be used up once and shall not be retained. The bacterial viability will resume after 1-2 generation of recovery. Please operate in strict accordance with this instruction, otherwise the replacement of bacteria are not be available in case of aberrant growth and loss of viability.
Growth conditions:37 ℃, aerobic, nutrient agar medium. Nutritional agar medium: beef paste 3.0g, peptone 10.0g,NaCl 5.0g, agar 20.0g (not included in liquid medium), distilled water 1.0L,pH7.0. 121 ℃,15min.
Recovery steps:
(1)Prepare a flask of NB liquid media or two NA agar plates.
(2) Open it in biosafety cabinet, heat the tip of ampoule in a flame, quickly drop sterile water to creak it, then break it with forceps;
(3)Draw 0.5mL of liquid medium into the freeze dried ampoule,make the strain pellet fully dissolved. transfer the liquid suspension to the liquid media, and culture in plate shaker at 37℃ (140r/min); or directly dispense 200ul of the liquid suspension into a NA agar plate evenly, then put the plates in incubator at 37℃ for 18-24 hours.
Recovery record: According to the recovery instructions, the results of the recovery are reported as follows:

| item | test results |
| Viability: | good viability, in 20hNB bacterial fluid turbidity; The bacterial liquid is marked NA plate with obvious colony |
|
colony morphology: (above) |
size: medium shape: round edge: irregular transparency: opaque Color: milky white uplift: middle raised surface: smooth texture: moist |
| conclusion: | good viability, and colony morphology is not abnormal, completely consistent with the above figure, qualified recovery |
Acinetobacter baumannii Bouvet and Grimont(Acinetobacter baumannii Bouvet and Grimont)
254392
Acinetobacter baumannii Bouvet and Grimont(Acinetobacter baumannii Bouvet and Grimont)
365320
Acinetobacter baumannii Bouvet and Grimont(Acinetobacter baumannii Bouvet and Grimont)
380823
Acinetobacter baumannii Bouvet and Grimont(Acinetobacter baumannii Bouvet and Grimont)
382292
Acinetobacter baumannii Bouvet and Grimont(Acinetobacter baumannii Bouvet and Grimont)
390681
Acinetobacter baumannii Bouvet and Grimont(Acinetobacter baumannii Bouvet and Grimont)
285982