BeNa Culture Collection
info@bncc.com
| Subculture procedure | ① Dissolve the cryovial in a water bath (mold at 30 ℃) and shake rapidly to dissolve; ② Wipe the outer wall of the cryovial 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 | Spread growth, filamentous, irregular edges, opaque, gray white front, flat shape, rough surface, wrinkled surface, dry texture, purity: pure |
| Sharing mode | Public welfare sharing |
Panus conchatus
Storage conditions : 2~8 ℃
No. : 336325
Product format : agar slant in 14mm test tube
Validity period: 30 days
Biosafety level : 1,handle in ultra-clean table or 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 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 lose of viability.
Growth Conditions :25-28 ℃, aerobic, integrated PDA,6d. Comprehensive PDA: potato boil 1.0L, glucose 20.0g,KH2PO4 3.0g,MgSO4 & middot;7H2O 1.5g, vitamin B1 trace, agar 20.0g,pH 6.0 & plusmn;0.2. Sterilization at 121 ℃ for 15min. Potato boiling liquid: weigh 200g of peeled potato pieces, boil in boiling water for 30min, and collect the filtrate to a constant volume of 1.0L.
Recovery steps:
(1)Prepare 1-2 pieces of PDA plates;
(2)Sterilize the surface of test tube for the agar slant, open it in the biosafety cabinet;
(3)Cut into the pieces with aseptic inoculation hoe and inoculation shovel (see attached page). the size of square pieces is 0.5 × 0.5cm2;
(4)Lay flat the small pieces to the center of the agar plate;
(5)Put the plates under the above culture conditions, and the strains can be used when they grow.
Recovery record: According to the recovery instructions, the results of the recovery are reported as follows:

| Item | test results |
| viability | good viability, 6 days, strain layer is obvious |
| colony morphology | small filamentous fungi have obvious colonies, white, dense and low flat on the integrated PDA medium, spreading and growing to concentric circles at the edge of the plate, and the back of the medium is light yellow. |
| conclusion | good viability, no abnormal colony morphology, qualified |