Mucor racemosa|189210 |BNCC

BeNa Culture Collection

Mucor racemosa-BNCC
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  • Mucor racemosus-BNCC

Mucor racemosus

Literatures(1)
  • Price: Contact
  • number:189210
  • Form:
    Spread and grow, produce a large number of spores, produce gray spores, irregular edges, opaque, gray mycelium, purity: pure
Standard strain Quantitative strain DNA extraction
Package:
Essential Information References Certificate Related Products
Mucor racemosus
Subculture procedure ① Prepare the above two tablets; 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 pour it into the freeze-drying tube to dissolve and mix thoroughly; ④ Transfer 0.2mL of bacterial suspension into a Agar plate, apply evenly, and repeat twice to obtain two plates; ⑤ Place the petri dish under the above cultivation conditions for cultivation, and once the bacterial strain grows, it can be used.
Growth conditions 28 ℃; 3-5 days; aerobic;
Storage conditions 2-8 ℃
Safety level 1
morphology Spread and grow, produce a large number of spores, produce gray spores, irregular edges, opaque, gray mycelium, purity: pure
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Mucor racemosus

No.: 189210

Storage conditions: 2~8 ℃

Product format: freeze dried,200ul

Validity period: 24 months

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. 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 ℃, aerobic, integrated 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 2 pieces of PDA plates or 2 agar slants; 

(2)Open the ampoule in the biosafety cabinet, heat the tip of ampoule 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; or transfer appropriate solution to 
the agar slant.    
(4)Place the plates uprightly and agar slant obliquely 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 result
viability good viability,in 4 days plate colony is obvious
colony morphology:

The morphology of bacteria is obviously visible in the integrated PDA agar medium,

The colony is loose flocculent, initially white, then light yellow to brown gray, and grows rapidly.

conclusion:

good viability, no abnormality in colony morphology, completely consistent with the above figure, qualified

 

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