Fusarium oxysporum|143058 |BNCC

BeNa Culture Collection

Fusarium oxysporum-BNCC
  • BNCC
  • Fusarium proliferatum-BNCC

Fusarium proliferatum

Literatures(3)
  • Price: Contact
  • number:143058
  • Form:
    Small filamentous fungi with visible colonies on PDA medium, white, dense, and cotton like hyphae
Standard strain Quantitative strain DNA extraction
Package:
Essential Information References Certificate Related Products
Fusarium proliferatum
Subculture procedure ① Prepare 1-2 of the above plates; ② After disinfecting the inclined surface of the test tube, open it in the safety cabinet; ③ Cut small square blocks of 0.5 × 0.5cm2 using a sterile inoculation hoe and inoculation shovel (see attached page); ④ Place the small square block flat on the center of the Agar plate and onto the surface of the agar; ⑤ Cultivate the flat Agar plate under the above cultivation conditions, and the strain can be used once it grows.
Growth conditions 28 ℃; 5-7 days; aerobic;
Storage conditions -80 ℃
Safety level 1
morphology Small filamentous fungi with visible colonies on PDA medium, white, dense, and cotton like hyphae
Sharing mode Public welfare sharing

Fusarium proliferatum

Storage conditions: 2~8 ℃

No. : 143058

product form:agar slant in 14mm test tube

Validity period : 30 days

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

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 :26-28 ℃, aerobic, integrated PDA. Comprehensive PDA: potato boiling juice 1000mL, potassium dihydrogen phosphate 3.0g, magnesium sulfate heptahydrate 1.5g, glucose 20.0g, vitamin B1 10mg, agar 20g,pH natural. 121 ℃,15min. 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.

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, and the strains can be used when they grow.

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

                                

item test result
viability good viability,in 6 days plate colony is obvious
colony morphology: small filamentous fungi, colonies are obviously visible on comprehensive PDA medium, hyphae are white, dense and cotton wool-like.
Conclusion: good viability, no abnormal colony morphology, completely consistent with the above figure, qualified

 

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