Aspergillus fumigatus|356064 |BNCC

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Aspergillus fumigatus

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	37 ℃; 5-7 days; aerobic;
Storage conditions	2-8 ℃
Safety level	1
morphology	Small filamentous fungi, with obvious colonies on YGC medium, initially white hyphae, dense and vigorous, and later producing blue gray spores that grow all over the Agar plate. The back of the medium is yellow
Sharing mode	Public welfare sharing

Aspergillus fumigatus

Storage conditions: 2~8 ℃

No. 356064

Product format: freeze dried, 200ul

Validity : 6 years

Biosafety level: 1 , handle in ultra-clean 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 agar plate 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:37 ℃, aerobic, 5-7 days, acetic acid bacteria medium (YGC): yeast extract 5.0g, glucose 50.0g, agar 15.0g (not included in liquid medium),CaCO3 12.5g (not included in liquid medium), distilled water 1.0L. pH 6.6 - 7.0. Sterilization at 121 ℃ for 15min.

Recovery steps:
(1) Prepare 1-2 of above mentioned plates;
(2) Open it in the biosafety cabinet, sterilize of the ampoule, heat the tip in a flame, quickly drop sterile water to creak it, then break it with forceps;
(3) Draw 0.5ml of sterile water into the freeze dried ampoule, make it fully dissolved, and distribute the solution to the plates well in 200ul/plate;
(4) Put the plates under the above culture conditions for cultivation for 5-7 days.
Recovery record: According to the recovery instructions, the results of the recovery are reported as follows:

Item	test results
viability:	good viability， in 5-7days strain layer is obvious
colony morphology: (above)	small filamentous fungi with obvious colonies on YGC medium, white hyphae at the initial stage, dense and vigorous, and brown spores all over the plate later.
Conclusion:	good viability, no abnormal colony morphology, qualified

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