Aspergillus nidulans|190203 |BNCC

BeNa Culture Collection

Aspergillus nidulans-BNCC
  • BNCC
  • Aspergillus nidulans-BNCC

Aspergillus nidulans

  • Price: Contact
  • number:190203
  • Form:
    Spread and grow on CPDA, with white hyphae in the early stage and a large number of spores in the later stage, producing yellow spores with irregular edges, opacity, yellow front, flat shape, rough surface, dark surface, dry texture, purity: pure
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Aspergillus nidulans
Subculture procedure ① Prepare 1-2 plates as 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 petri dish under the above cultivation conditions for cultivation, and once the bacterial strain grows, it can be used.
Growth conditions 28 ℃; 5-7 days; aerobic
Storage conditions 2-8 ℃
Safety level 1
morphology Spread and grow on CPDA, with white hyphae in the early stage and a large number of spores in the later stage, producing yellow spores with irregular edges, opacity, yellow front, flat shape, rough surface, dark surface, dry texture, purity: pure
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1. Description 

1. Name: spergillus nidulans

2. BNCC No.: 190203

3. Biosafety level:  4

2. Storage conditions:

Storage of freezed dried ampoule and agar slant at 2°C to 8°C.

3. Growth Conditions: 

1. Comprehensive PDA:20% potato juice 1L, glucose 20g ,KH2PO4 3g, MgSO4.7H2O 1.5g, thiamine trace, agar 15g,pH natural.

2. Atmosphere: aerobic

3. Temperature:  28-30 ℃

4. Notes: 

1.Normal culturing time, 24-48hours for bacterial, 72 hours for yeast, 5-7days for mould, 7-10days for fungal.

2.Agar slant shall be inoculated asap, and do not keep the storage for more than 3 months.

3.Please recover the strains in strict accordance with this instruction, otherwise the replacement of the strain are not be available in case of viability loss caused by different media or growth conditions.

4.Waste generated from the handling process should be discarded after high-pressure sterilization.

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