Microsporidia canis|259680 |BNCC

BeNa Culture Collection

Microsporidia canis-BNCC
Microsporidia canis-BNCC
Microsporidia canis-BNCC
  • BNCC
  • Microsporum canis Bodin anamorph-BNCC
  • Microsporum canis Bodin anamorph-BNCC
  • Microsporum canis Bodin anamorph-BNCC

Microsporum canis Bodin anamorph

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  • Price: Contact
  • number:259680
  • Form:
    Small filamentous fungi grow well on comprehensive PDA medium, with a white front and spreading growth, and a yellow back
Standard strain Quantitative strain DNA extraction
Package:
Essential Information References Certificate Related Products
Microsporum canis Bodin anamorph
Subculture procedure ① Prepare 1-2 tablets mentioned above; ② After disinfecting the surface of the ampoule tube, open it in a safety cabinet, burn the top with an alcohol lamp, quickly drip sterile water to break it, and then use tweezers to crush it; ③ Take 0.5mL of sterile water and transfer it into a freeze-drying tube. After fully dissolving the bacterial powder, transfer it into a Agar plate at a rate of 200 μ L per piece and apply evenly; ④ Place the agar plate under the above cultivation conditions for cultivation.
Growth conditions 28 ℃; 5-7 days; aerobic
Storage conditions 2-8 ℃
Safety level 2
morphology Small filamentous fungi grow well on comprehensive PDA medium, with a white front and spreading growth, and a yellow back
Sharing mode Public welfare sharing

Microsporum canis Bodin anamorph

Storage conditions: 2~8 ℃

No. 259680

Product format: freeze dried,200ul

Validity period: 6 years

Biosafety  level:  2, handle in 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: 28°C, aerobic, integrated PDA, 5-7 days. Comprehensive PDA: Potato cooking liquid 1.0L, glucose 20.0g, KH2PO4 3.0g, MgSO4 7H2O 1.5g, trace amount of vitamin B1, agar 20.0g, pH 6.0±0.2. Sterilize at 121℃ for 15min. Potato cooking liquid: Weigh 200g peeled potato pieces, boil in boiling water for 30min, collect the filtrate and dilute to 1.0L.

Recovery steps:

(1)  Prepare 1-2 of above mentioned plates; 

(2)  Sterilize the plate surface, open it in biosafety cabinet;

(3)  Pick up 1-2 rings of plate colonies by inoculation loop, inoculate to fresh medium;

(4) 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 on the integrated PDA medium. The mycelium in the plate layer is white and dense, spreading and growing, producing gray-white spores in the later stage, and the back of the medium is yellow.
Conclusion good viability, no abnormal colony morphology, qualified
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