Streptomyces|341716 |BNCC

BeNa Culture Collection

Streptomyces-BNCC
Streptomyces-BNCC
Streptomyces-BNCC
  • BNCC
  • Alternaria alternata-BNCC
  • Alternaria alternata-BNCC
  • Alternaria alternata-BNCC

Alternaria alternata

Literatures(3)
  • Price: Contact
  • number:341716
  • Form:
    Small filamentous fungi have obvious colonies on PDA medium, appearing flocculent and growing rapidly. They are initially dark white and turn brown as they age; The back is brown
Standard strain Quantitative strain DNA extraction
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Alternaria alternata
Subculture procedure ① Prepare 1-2 of the above plates; ② After disinfecting the inclined surface of the test tube, open it in the safety cabinet; ③ Cut small square blocks of 0.5 × 0.5cm2 using a sterile inoculation hoe and inoculation shovel (see attached page); ④ Place the small square block flat on the center of the Agar plate and onto the surface of the agar; ⑤ Cultivate the flat Agar plate under the above cultivation conditions, and the strain can be used once it grows.
Growth conditions 28; 4-7 days; aerobic;
Storage conditions 2-8 ℃
Safety level 2
morphology Small filamentous fungi have obvious colonies on PDA medium, appearing flocculent and growing rapidly. They are initially dark white and turn brown as they age; The back is brown
Sharing mode Public welfare sharing

Alternaria alternata

Description 

1, BNCC No.: 341716

2. Biosafety level: 3

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

Growth Conditions 

1. Comprehensive PDA:20% potato juice 1L, glucose 20g, KH2PO43 g, MgSO4.7H2O 1.5g, thiamine trace, agar 15g,pH natural.

2. Atmosphere: aerobic

3, Temperature:  28 ℃

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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