Rhodococcus faecalis|337333 |BNCC

BeNa Culture Collection

Rhodococcus faecalis-BNCC
Rhodococcus faecalis-BNCC
Rhodococcus faecalis-BNCC
  • BNCC
  • Cryptococcus laurentii-BNCC
  • Cryptococcus laurentii-BNCC
  • Cryptococcus laurentii-BNCC

Cryptococcus laurentii

Literatures(1)
  • Price: Contact
  • number:337333
  • Form:
    Colony diameter: 1-2 mm; circular shape with neat margins; opaque, creamy-white surface; central elevation; smooth texture; easily liftable; G+ (blue-violet); cocci; purity: pure
Standard strain Quantitative strain DNA extraction
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Cryptococcus laurentii
Subculture procedure ① Prepare 1-2 of the above plates; 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 30 ℃; 24-48 hours; aerobic
Storage conditions 2-8 ℃
Safety level 1
morphology Colony diameter: 1-2 mm; circular shape with neat margins; opaque, creamy-white surface; central elevation; smooth texture; easily liftable; G+ (blue-violet); cocci; purity: pure
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Cryptococcus laurentii

1.Description

1. BNCC No.:  337333 

2. Biosafety level: 4

2.Storage conditions:

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

3.Growth Conditions

1. YM medium: yeast extract, 3.0g malt extract, 3.0g glucose, 10.0g protein block, 5.0g agar, 20.0g distilled water 1000 ml ,pH 6.2 +/- 0.2

2.Atmosphere: aerobic

3.Temperature:  25-28 ℃

4.Notes:

1.Normal culturing time, 1-2days for bacterial, 3 days 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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