Red Trichophyton|313807 |BNCC

BeNa Culture Collection

Red Trichophyton-BNCC
Red Trichophyton-BNCC
Red Trichophyton-BNCC
  • BNCC
  • Trichophyton rubrum(Castellani) Sabouraud-BNCC
  • Trichophyton rubrum(Castellani) Sabouraud-BNCC
  • Trichophyton rubrum(Castellani) Sabouraud-BNCC

Trichophyton rubrum(Castellani) Sabouraud

  • Price: Contact
  • number:313807
  • Form:
    Small filamentous fungi grow well on comprehensive PDA medium, with white, filamentous, and spreading growth on the front of the medium and yellow on the back of the medium
Standard strain Quantitative strain DNA extraction
Package:
Essential Information Certificate Related Products
Trichophyton rubrum(Castellani) Sabouraud
Subculture procedure ① Dissolve the Frozen vial in a water bath (fungi at 30 ℃) and shake rapidly to dissolve; ② Wipe the outer wall of the Frozen vial with an alcohol swab for disinfection, and then transfer it to a safe cabinet for operation; ③ Unscrew the tube cap, aspirate all the dissolved solution, and transfer it into 1-2 agar plates; ④ After uniform coating, transfer to the above cultivation conditions for cultivation.
Growth conditions 28 ° C; 5-7 days; aerobic
Storage conditions -80 ℃
Safety level 2
morphology Small filamentous fungi grow well on comprehensive PDA medium, with white, filamentous, and spreading growth on the front of the medium and yellow on the back of the medium
Sharing mode Public welfare sharing

Trichophyton rubrum

No.: 313807

Storage conditions: 2~8 ℃

Product format: agar slant in 14mm test tube

Validity period: growing culture in 30 days

Biosafety  level: 2, handle in 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:25-28 ℃, aerobic, integrated PDA,5-7 days. Comprehensive PDA: potato boil 1.0L, glucose 20.0g,KH2PO4 3.0g,MgSO4·7H2O 1.5g, vitamin B1 trace, agar 20.0g,pH 6.0±0.2. Sterilization at 121 ℃ for 15min. Potato boiling liquid: weigh 200g of peeled potato pieces, boil in boiling water for 30min, and collect the filtrate to a constant volume of 1.0L.

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 results
viability
 
good viability, in 5-7 days plate colony is obvious
colony morphology

small filamentous fungi with obvious colonies and villous on integrated PDA culture medium,

white with radial stripes and orange on the back of the culture medium.

conclusion good viability, no abnormal colony morphology, qualified
Download certificate
Please set your password: