Beauveria bassiana|356392 |BNCC

BeNa Culture Collection

Beauveria bassiana-BNCC
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  • Beauveria felina (DC.) J.W. Carmich., The-BNCC

Beauveria felina (DC.) J.W. Carmich., The

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  • number:356392
  • Form:
    On the comprehensive potato dextrose agar medium, it exhibits spreading growth with white, velvety, and fine mycelia. The surface is wrinkled and firm in texture, while the reverse side appears pale yellow.
Standard strain Quantitative strain DNA extraction
Package:
Essential Information Certificate Related Products
Beauveria felina (DC.) J.W. Carmich., The
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 On the comprehensive potato dextrose agar medium, it exhibits spreading growth with white, velvety, and fine mycelia. The surface is wrinkled and firm in texture, while the reverse side appears pale yellow.
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Beauveria felina

Storage conditions: 2~8 ℃

No. 356392

Product format: agar slant in 14mm test tube

Validity period: growing culture, in 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.

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, in 7 days plate colony is obvious
colony morphology: (above) Small filamentous fungi have obvious colonies, gray-white, wrinkled, and light yellow on the back of the medium on the integrated PDA medium.
Conclusion good viability, no abnormal colony morphology, qualified
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