Rhizophora|337556 |BNCC

BeNa Culture Collection

Rhizophora-BNCC
Rhizophora-BNCC
Rhizophora-BNCC
  • BNCC
  • Akanthomyces sp.-BNCC
  • Akanthomyces sp.-BNCC
  • Akanthomyces sp.-BNCC

Akanthomyces sp.

Literatures(1)
  • Price: Contact
  • number:337556
  • Form:
    Small filamentous fungi have obvious colonies on comprehensive PDA culture medium, white hyphae, dense and flat, slow spreading and growth, and a light yellow color on the back of the culture medium
Standard strain Quantitative strain DNA extraction
Package:
Essential Information References Certificate Related Products
Akanthomyces sp.
Subculture procedure ① Prepare 1-2 tablets mentioned above; 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 2-8 ℃
Safety level 1
morphology Small filamentous fungi have obvious colonies on comprehensive PDA culture medium, white hyphae, dense and flat, slow spreading and growth, and a light yellow color on the back of the culture medium
Sharing mode Public welfare sharing

Fusarium nivale.

Storage conditions: 2~8 ℃

No.: 337556

Product format: agar slant in 14mm test tube 

Validity period: Activated form within 30 days

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 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 lose of viability.

Growth conditions:28 ℃, aerobic, integrated PDA,5-7 days. Comprehensive PDA: 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.

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 5-7 days strain layer is obvious
colony morphology small filamentous fungi have obvious colonies, white hyphae, dense and low flat on the integrated PDA medium, spreading to the edge of the plate without spores, and the back of the medium is light yellow.
conclusion good viability, no abnormal colony morphology, qualified
Download certificate
Please set your password: