BeNa Culture Collection
info@bncc.com
| Subculture procedure | ① Dissolve the frozen tube in a water bath (fungi at 30 ℃) and shake quickly to dissolve; ② Wipe the outer wall of the Frozen vial with an alcohol swab for disinfection, and then transfer it to a safe cabinet for operation; ③ Unscrew the tube cap, aspirate all the dissolved solution, and transfer it into 1-2 agar plates; ④ After uniform coating, transfer to the above cultivation conditions for cultivation. |
| Growth conditions | 28 ℃; 5-7 days; aerobic |
| Storage conditions | -80℃ |
| Safety level | 1 |
| morphology | Small filamentous fungi with distinct colonies on PDA medium, gray brown in color, dense and vigorous, spreading and growing towards the edge of the Agar plate, and black on the back of the medium |
| Sharing mode | Public welfare sharing |
Bipolaris sorokiniana
Storage conditions : 2~8 ℃
No. : 185286
Product format :freeze dried, 200ul
Validity : 6 years
Biosafety level : 1, handle in ultra-clean table or safety cabinet
Receiving notice: if any abnormality is found on the day of receiving goods, please contact customer service within 24 hours. if it is overdue, it will be regarded as good receiving goods. Dry powder shall not be retained after one use, and can be used after activating for 1~2 generations. please refer to the attached page for the use of inclined planes and flat plates. Please activate in strict accordance with this instruction, otherwise the replacement service will not be provided if the strain is abnormal and inactivated.
Growth conditions: 28 ℃, aerobic, PDA,5-7 days, PDA: potato boiling solution 1.0L, glucose 20.0g, agar 15.0g (not included in liquid medium), natural pH. Sterilization at 121 ℃ for 15min. Potato boiling solution: weigh 200g of peeled potato pieces, boil in boiling water for 30min, and collect filtrate to a constant volume of 1.0L.
Recovery steps:
(1)Prepare 1-2 of above mentioned plates;
(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 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 5-7days.

Recovery record: According to the recovery instructions, the results of the recovery are reported as follows
| Item | test results |
| viability | good viability, in 5-7 days strain layer become obvious |
| colony morphology: (above) | small filamentous fungi, with obvious colonies on PDA medium, gray-brown colonies, dense and vigorous, spreading round to the edge of the plate, and black on the back of the medium. |
| Conclusion: | good viability, no abnormal colony morphology, qualified |