Fungi|147484 |BNCC

BeNa Culture Collection

Fungi-BNCC
Fungi-BNCC
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  • BNCC
  • Mucor circinelloides-BNCC
  • Mucor circinelloides-BNCC
  • Mucor circinelloides-BNCC

Mucor circinelloides

Literatures(2)
  • Price: Contact
  • number:147484
  • Form:
    Spread growth, produce gray white spores, darker color, purity: pure
Standard strain Quantitative strain DNA extraction
Package:
Essential Information References Certificate Related Products
Mucor circinelloides
Subculture procedure ① Prepare one test tube containing 5-10 mL of liquid culture medium and two plates; 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 Transfer 0.5mL of liquid culture medium into a freeze-drying tube, dissolve it thoroughly, and then transfer it back into the liquid test tube, mixing well; ④ Transfer 0.2mL of bacterial suspension into a Agar plate, apply evenly, and repeat twice to obtain two plates; ⑤ Place all liquid test tubes and plates under the above cultivation conditions, and the bacterial strains can be used once they grow.
Growth conditions 28 ℃; 5-7 days; aerobic;
Storage conditions 2-8 ℃
Safety level 1
morphology Spread growth, produce gray white spores, darker color, purity: pure
Sharing mode Public welfare sharing

Mucor circinellolides

No.: 147484

Storage conditions: 2~8 ℃

Product format: freeze dried,200ul

Validity period: 6 years

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:28 ℃, aerobic, 5-7 days, comprehensive PDA agar medium: potato boiling juice 1000mL, potassium dihydrogen phosphate 3g, magnesium sulfate 1.5g, glucose 20g, vitamin B1 10mg, agar 20g,pH natural. Potato boiling solution: 200g of potato, peeled, cut into pieces, boiled in distilled water for 30min, constant volume of filtrate to 1000mL for later use. 121 ℃,15min.

activation steps:

① Prepare the above 2 plates;

②Open it in the safety cabinet, burn the top with an alcohol lamp, quickly drop sterile water to break it, and then break it with tweezers;

③ Suck 0.5mL of sterile water into the freeze-drying tube and mix well;

④ Absorb 0.2mL of bacterial suspension into the plate, coat evenly, repeat twice to obtain two plates;

⑤ All the plates are cultured under the above culture conditions, and the strains can be used when they grow out.

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

                                          

item test result
viability good viability, in 5-7 days strain layer become obvious,  colony is typical

colony morphology:

(above)

filamentous fungi have obvious colonies on comprehensive PDA culture medium,

hyphae are gray-white, dense/long, hyphae spread vigorously and produce gray-white spores.

conclusion: good viability, no abnormal colony morphology, qualified

 

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