Brown gill fungus|143315 |BNCC

BeNa Culture Collection

Brown gill fungus-BNCC
Brown gill fungus-BNCC
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  • Gloeophyllum trabeum-BNCC
  • Gloeophyllum trabeum-BNCC

Gloeophyllum trabeum

Literatures(5)
  • Price: Contact
  • number:143315
  • Form:
    Spread and grow, producing a large number of spores, producing gray white spores, purity: pure
Standard strain Quantitative strain DNA extraction
Package:
Essential Information References Certificate Related Products
Gloeophyllum trabeum
Subculture procedure ① Prepare 1-2 tablets 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 and grow, producing a large number of spores, producing gray white spores, purity: pure
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Gloeophyllum trabeum 

No.: 143315

Storage conditions: 2~8 ℃

Product format:agar slant in 14mm test tube

validity period: 30 days

Biosafety  level: 1, handle in ultra-clear table or safety cabinet

Receiving notice: if any abnormality is found on the day of receipt, please contact the customer service within 24 hours. If it is overdue, it is deemed that the bacteria are well. The freeze dried culture shall be used up once and shall not be retained. The bacterial viability will resume after 1-2 generation of recovery and can be used normally. Handling instructions of agar slant and suspension liquid is enclosed. Please operate in strict accordance with this instruction, otherwise the replacement of bacteria are not be available in case of aberrant growth and loss of viability.

Growth conditions:25-28 ℃, aerobic, comprehensive PDA. Comprehensive PDA:20% potato juice 1L, glucose 20g ,KH2PO4 3g, MgSO4.7H2O 1.5g, thiamine trace, agar 15g,pH natural.

Recovery steps:

(1)Prepare 1-2 pieces of PDA plates; 

(2)Sterilize the surface of test tube for the agar slant, open it in the biosafety cabinet; 

(3) Cut into the pieces with aseptic inoculation hoe and inoculation shovel (see attached page). the size of square pieces is 0.5 × 0.5cm2; 

(4) Lay flat the small pieces to the center of the agar plate;

(5) Put the plates under the above culture conditions for 5-7 days. Or contact our technicians for the inoculation of agar slant - filamentous fungi.

Recovery record:  According to the recovery instructions, the results of the recovery are reported as follows:

                                                    

item test results
viability: good viability, in 7 days plate colony obvious
colony morphology:

small filamentous fungi, colonies are obviously visible on comprehensive PDA culture medium,

mycelium is light yellowish brown, with blunt edges, fluffy, slightly ringed, and thick colonies.

conclusion: good viability, no abnormal colony morphology, completely consistent with the above figure, qualified

 

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