Parasitic Aspergillus|194138 |BNCC

BeNa Culture Collection

Parasitic Aspergillus-BNCC
  • BNCC
  • Aspergillus parasiticus-BNCC

Aspergillus parasiticus

Literatures(3)
  • Price: Contact
  • number:194138
  • Form:
    Spread growth, white filamentous in the early stage, producing a large number of yellow spores in the later stage, white on the reverse side, purity: pure
Standard strain Quantitative strain DNA extraction
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Aspergillus parasiticus
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 growth, white filamentous in the early stage, producing a large number of yellow spores in the later stage, white on the reverse side, purity: pure
Sharing mode Public welfare sharing

1.Description 

1. Name:Aspergillus parasiticus

2. BNCC No.: 194138 

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 3.0g,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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