Streptococcus pyogenes|185918 |BNCC

BeNa Culture Collection

Streptococcus pyogenes-BNCC
  • BNCC
  • Streptococcus pyogenes-BNCC

Streptococcus pyogenes

Literatures(1)
  • Price: Contact
  • number:185918
  • Form:
    The colony diameter is 1-2mm, circular, with irregular edges, opaque, gray white on the front, raised in the middle, smooth and bright on the surface, moist texture, easy to pick up, G+(blue purple), cocci, purity: pure
Standard strain Quantitative strain DNA extraction
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Streptococcus pyogenes
Subculture procedure ① Prepare 2 plates; 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. After fully dissolving, mix well; ④ Transfer 0.2mL of bacterial suspension into a Agar plate, apply evenly, and repeat twice to obtain two plates; ⑤ Place all the plates under the above cultivation conditions, and once the strains grow, they can be used.
Growth conditions 37 ℃; 18-24h;5%CO2;
Storage conditions 2-8 ℃
Safety level 2
morphology The colony diameter is 1-2mm, circular, with irregular edges, opaque, gray white on the front, raised in the middle, smooth and bright on the surface, moist texture, easy to pick up, G+(blue purple), cocci, purity: pure
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Streptococcus pyogenes

No.: 185918

Storage conditions: 2~8 ℃

Product format: freeze dried,200ul

Validity period: 6 years

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.

Recovery steps:

(1)Prepare 1-2 of above mentioned plates; 

(2)Open it in the biosafety cabinet, sterilize of the ampoule, heat the tip 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; 

(4)Put the plates under the above culture conditions for cultivation for 18-24 hours.

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

                                         

item test result
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: neat transparency: opaque, hemolytic

color: milky white uplift: middle raised surface: bright and smooth texture: moist and viscous

conclusion: good viability, no abnormal colony morphology, qualified

 

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