Aspergillus oryzae|190278 |BNCC

BeNa Culture Collection

Aspergillus oryzae-BNCC
Aspergillus oryzae-BNCC
Aspergillus oryzae-BNCC
  • BNCC
  • Aspergillus tubingensis-BNCC
  • Aspergillus tubingensis-BNCC
  • Aspergillus tubingensis-BNCC

Aspergillus tubingensis

Literatures(1)
  • Price: Contact
  • number:190278
  • Form:
    Proliferative growth with white filamentous morphology, producing yellowish-brown spores, light yellow in color, purity: pure.
Standard strain Quantitative strain DNA extraction
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Essential Information References Certificate Related Products
Aspergillus tubingensis
Subculture procedure ① Prepare 1-2 plates as mentioned above; ② Open the 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 two plates, each Agar plate containing about 200 μ L, 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 ℃; 3-5 days; aerobic
Storage conditions 2-8 ℃
Safety level 1
morphology Proliferative growth with white filamentous morphology, producing yellowish-brown spores, light yellow in color, purity: pure.
Sharing mode Public welfare sharing

1. Description 

1. Name:  Aspergillus tubingensis

2. BNCC No.:  190278

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, Czapek ' Sagar: sucrose 30.0g,NaNO3 3.0 g,MgSO4·7H2O 0.5 g,KCl 0.5 g,FeSO4·4H2O 0.01 g,K2HPO4 1.0 g, agar 15.0g, distilled water 1.0 L,pH 6.0-6.5.

2. Atmosphere: aerobic

3. Temperature:  25-28 ℃

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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