Microbacterium|196305 |BNCC

BeNa Culture Collection

Microbacterium-BNCC
Microbacterium-BNCC
Microbacterium-BNCC
  • BNCC
  • Microbacterium sp.-BNCC
  • Microbacterium sp.-BNCC
  • Microbacterium sp.-BNCC

Microbacterium sp.

  • Price: Contact
  • number:196305
  • Form:
    The colonies are 1-2 mm, circular, convex, opaque, yellow colonies with entire margins and a smooth, glistening, moist texture that is easily picked up.
Standard strain Quantitative strain DNA extraction
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Essential Information Certificate Related Products
Microbacterium sp.
Subculture procedure ① Prepare 1-2 tablets 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 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 30 ℃, 2-3 days, aerobic
Storage conditions 2-8 ℃
Safety level 1
morphology The colonies are 1-2 mm, circular, convex, opaque, yellow colonies with entire margins and a smooth, glistening, moist texture that is easily picked up.
Sharing mode Public welfare sharing

1.Description 

1.Name: Microbacterium sp.

2. BNCC No.:196305

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. LB medium: peptone 10.0g, yeast powder 5.0g,NaCl 10.0g, agar 15.0g, distilled water 1.0L,pH7.0.

2. Atmosphere:aerobic

3. Temperature: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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