Cicada flower 1-13|116724 |BNCC

BeNa Culture Collection

Cicada flower 1-13-BNCC
Cicada flower 1-13-BNCC
Cicada flower 1-13-BNCC
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  • Isaria cicadae Miq.-BNCC
  • Isaria cicadae Miq.-BNCC
  • Isaria cicadae Miq.-BNCC

Isaria cicadae Miq.

Literatures(2)
  • Price: Contact
  • number:116724
  • Form:
    Spreading growth, filamentous, irregular margin, opaque; on CPDA medium, the mycelium is raised, obverse gray-white, surface rough and wrinkled, texture dry; purity: pure.
Standard strain Quantitative strain DNA extraction
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Essential Information References Certificate Related Products
Isaria cicadae Miq.
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 Liquid nitrogen
Safety level 1
morphology Spreading growth, filamentous, irregular margin, opaque; on CPDA medium, the mycelium is raised, obverse gray-white, surface rough and wrinkled, texture dry; purity: pure.
Sharing mode Public welfare sharing

Isaria cicadae Miq.

Storage conditions: 2~8 ℃

No. 116724

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.

Growte conditions :28 ℃, aerobic, integrated PDA. Comprehensive PDA: potato boiling juice 1000mL, potassium dihydrogen phosphate 3.0g, magnesium sulfate heptahydrate 1.5g, glucose 20.0g, vitamin B1 10mg, agar 20g,pH natural. 121 ℃,15min. Potato boiling solution: 200g of potato, peeled, cut into pieces, boiled in distilled water for 30min, constant volume of filtrate to 1000mL for later use. 121 ℃,15min.

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 for 5-7 days. You can also contact customer service for information "Inclined Transfer Method-Filamentous Fungi".

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, colonies are obviously visible on comprehensive PDA medium, hyphae are white, thick, and fold on the back.
Conclusion: good viability, no abnormal colony morphology, completely consistent with the above figure, qualified
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