BeNa Culture Collection
Culture medium | Columbia blood plate (CA-B): casein pancreatin digest 10.0g, cardiopancreatin digest 3.0g, corn starch 1.0g, meat gastric enzyme digest 5.0g, yeast extract 5.0g, sodium chloride 5.0, agar 20.0g, distilled water 1.0L,pH 7.3±0.2. After sterilization at 121 ℃ for 15min, cool to 55 ℃, add 5% sterile defibrated sheep blood, shake well, pour the plate and cool it for later use. |
Subculture procedure | (1) Prepare 2 plates; (2) Open it in the safety 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 culture medium into a freeze dried ampoule, fully rehydrate, inoculate a plate with the solution at 200ul/plate; (4) Put the plate under the above culture conditions for 8-10 days. |
Growth conditions | 37 ℃,8-10 days, anaerobic |
Storage conditions | 2-8 ℃ |
morphology | Colony diameter is 1-2mm, irregular shape, irregular edge, opaque, gray-white front, convex in the middle, bright surface, smooth surface, sticky texture, G-(red), bacilli |
Separation substrate | Human gingival sulcus |
application | Quality control strain |
Sharing mode | Public welfare sharing |
Porphyromonas gingivalis
Storage conditions: 2~8 ℃
No. 236547
Product format: freeze dried,200ul
Validity period: 6 years
Biosafety level: 2, handle in safety cabinet
Receiving 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 and can be used normally. Handling instructions of agar slant and suspension liquid is enclosed. 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 ℃, anaerobic, Colombian blood plate (ready-to-use type),8-10 days.
Recovery steps:
(1) Prepare 1-2 of above mentioned plates(place in anaerobic environment for 24hours before usage);
(2) Open it in the biosafety cabinet, sterilize of the ampoule, heat the tip in a flame, quickly drop sterile water to creak it, then break it with forceps;
(3) Draw 0.5ml of sterile water(place in anaerobic environment for 24 hours before usage) into the freeze dried ampoule, make it fully dissolved, and distribute the solution to the plates well in 200ul/plate;
(4) Put the plates under the above culture conditions for cultivation for 8-10 days.
Recovery record: According to the recovery instructions, the results of the recovery are reported as follows:
Item | test results |
viability | good viability,in 10 days strain layer become obvious, colony is typical |
colony morphology: (above) |
Size: 1-2mm Shape: Irregular Edge: Irregular Transparency: Opacity color: gray-black bulge: middle bulge surface: bright and smooth texture: viscous |
Conclusion | good viability, no abnormal colony morphology, qualified |