Aspergillus ochraceus|187409 |BNCC

BeNa Culture Collection

Aspergillus ochraceus-BNCC
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  • Aspergillus ochraceus-BNCC

Aspergillus ochraceus

Literatures(6)
  • Price: Contact
  • number:187409
  • Form:
    Spread growth, filamentous, irregular edges, initially white hyphae on the front, later producing yellow spores, yellow on the back
Standard strain Quantitative strain DNA extraction
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Essential Information References Certificate Related Products
Aspergillus ochraceus
Subculture procedure ① Prepare the above two tablets; 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 2 plates at a rate of 200 μ L per Agar plate 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 growth, filamentous, irregular edges, initially white hyphae on the front, later producing yellow spores, yellow on the back
Sharing mode Public welfare sharing

1. Description 

1. Name: Aspergillus ochraceus

2. BNCC No.: 187409 

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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