Bacillus thuringiensis insecticidal subspecies|223176 |BNCC

BeNa Culture Collection

Bacillus thuringiensis insecticidal subspecies-BNCC
Bacillus thuringiensis insecticidal subspecies-BNCC
  • BNCC
  • Bacillus thuringiensis subsp. entomocidus-BNCC
  • Bacillus thuringiensis subsp. entomocidus-BNCC

Bacillus thuringiensis subsp. entomocidus

Literatures(2)
  • Price: Contact
  • number:223176
  • Form:
    Size: 2-4mm
Standard strain Quantitative strain DNA extraction
Package:
Essential Information References Certificate Related Products
Bacillus thuringiensis subsp. entomocidus
Subculture procedure ① Prepare 1 tube containing 5–10 mL liquid medium and 2 plates; ② Open in a safety cabinet, cauterize the top with an alcohol lamp, then quickly add sterile water to rupture it; break it into pieces with forceps; ③ Pipette 0.5mL liquid medium into the freeze-dried vial, dissolve completely, then return to the liquid test tube and mix thoroughly; ④ Pipette 0.2mL bacterial suspensioninto each Agar plate, spread evenly, and repeat twice to obtain two plates; ⑤ Incubate all liquid tubes and plates under the specified conditions. The culture is ready for use once growth appears.
Growth conditions 30°C, 18-24h, aerobic
Storage conditions 2-8°C
Safety level 1
morphology Size: 2-4mm
Sharing mode Public welfare sharing

Bacillus thuringiensis subsp.

BNCC No.: 223176

Storage conditions: 2~8 ℃

Product format: freeze dried, 200ul 

Validity period: 6 years

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. 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:30°C, aerobic, nutrient agar medium, 18-24h. Nutritional agar medium: beef paste 3.0g, peptone 10.0g,NaCl 5.0g, agar 20.0g (not included in liquid medium), distilled water 1.0L,pH7.0. 121 ℃,15min.

Recovery steps:

(1)Prepare a test tube containing 5-10mL of liquid culture medium and 2 plates; 

(2)Open it 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 liquid culture medium into a freeze dried ampoule, fully rehydrate and transfer the solution to the liquid test tube, mix evenly; 

(4)Inoculate a plate with 0.2mL of suspension liquid, repeat the step to obtain two plates; 

(5)Put all the liquid test tubes and plates under the above culture conditions for cultivation, 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 20h liquid medium become turbid, obvious strain layer occurs on the plate,colony is typical on marked plate.

colony morphology:

(above)

size: 2-4mm shape: round edge: false filamentous transparency: opaque

color: off-white uplift: middle raised surface: rough gray texture: dry easy to stir

conclusion: good viability, no abnormal colony morphology, qualified
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