Cordyceps farinosa|109763 |BNCC

BeNa Culture Collection

Cordyceps farinosa-BNCC
Cordyceps farinosa-BNCC
Cordyceps farinosa-BNCC
  • BNCC
  • Cordyceps farinosa-BNCC
  • Cordyceps farinosa-BNCC
  • Cordyceps farinosa-BNCC

Cordyceps farinosa

  • Price: Contact
  • number:109763
  • Form:
    Filamentous fungi, with obvious colonies, white color, dense and vigorous hyphae, protruding in the middle, rough surface, dry texture, poor spreadability, and light yellow color on the back of the culture medium
Standard strain Quantitative strain DNA extraction
Package:
Essential Information Certificate Related Products
Cordyceps farinosa
Subculture procedure ① Dissolve the frozen tube in a water bath (mold at 30 ℃, bacteria at 37 ℃) and shake quickly for dissolution; 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 cap of the tube, aspirate all the dissolved solution, and transfer it into 1-2 agar plates (approximately 200 μ L per plate); 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 Filamentous fungi, with obvious colonies, white color, dense and vigorous hyphae, protruding in the middle, rough surface, dry texture, poor spreadability, and light yellow color on the back of the culture medium
Sharing mode Public welfare sharing

Paecilomyces hepiali

Storage conditions : 2~8 ℃

No. 109763

Product format: agar slant in 14mm test tube

Validity period : 30 days

Biosafety  level: 1, handle in ultra-clear 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 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:25-28 ℃, aerobic, PDA,5-7 days. PDA: potato boil 1.0L, glucose 20.0g, agar 15.0g, natural pH. 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 result
viability good viability,in 6 days plate colony is obvious
colony morphology:

small filamentous fungi, with obvious colonies on PDA medium, bulging, smooth, cyan hyphae, folds on the front of the medium,

The back is light yellow and does not produce spores.

Conclusion: good viability, no abnormal colony morphology, qualified
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