Escherichia coli DH5α(pEX18TC)|BNCC359935 |BNCC

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Escherichia coli DH5α(pEX18TC)

Culture medium	Nutritional gravy medium (NA/NB): beef paste 3.0g, peptone 10.0g,NaCl 5.0g, agar 20.0g (without liquid medium), distilled water 1.0L,pH 7.0. Sterilization at 121 ℃ for 15min. [Note] Adding 5 mg MnSO4 · H2O to culture Bacillus is beneficial to produce spores.
Subculture procedure	(1) Prepare a test tube containing 5~10mL of liquid medium and 2 plates; (2) Open it in the safety 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.
Growth conditions	37 ℃;18-24h; Aerobic;
Storage conditions	2-8 ℃
application	Scientific research
Sharing mode	Public welfare sharing

Escherichia coli DH5α(pEX18TC)

Storage conditions : 2~8 ℃

No. : 359935

Product format :freeze dried, 200ul

Validity : 6 years

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 of agar plate 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.

Host bacteria:BNCC353719 DH5α.

Plasmid:BNCC360173 pEX18TC.

Medium: nutrient agar medium beef paste 3.0g, peptone 10.0g,NaCl 5.0g, agar 20.0g (not included in liquid medium), distilled water 1.0L,pH 7.0. Sterilization at 121 ℃ for 15min. Prokaryotic resistance: Tet

Growth conditions：37 ℃ aerobic 18-24h.

Recovery steps:

1. Prepare 1 sterile liquid test tube (including 5~10mL of culture medium) and 2 pieces of 90mm plate;

2. After disinfecting the surface of the ampoule tube, open it in the safety cabinet, burn the top with an alcohol lamp, quickly drop sterile water to break it, and then break it with tweezers;

3. suck 0.5mL of liquid culture medium and put it into the freeze-drying tube, fully dissolve it and return it to the liquid test tube again and mix well.

4. Draw the mixed solution from the test tube liquid to apply the flat plate, 200 & mu;L/piece;

5. Put all the test tubes and plates under the above specified conditions for cultivation. It is forbidden to seal and wind the plates. After 18-24 hours, observe the obvious turbidity of the culture medium and the growth of plate colonies or moss.

6. if the strain has not grown, it should continue to be cultured for 72h until a single colony or moss grows.

Plasmid purification:

1. pick a single colony and inoculate it into 50mL of liquid nutrient broth medium, and culture at 37 ℃ overnight;

2. according to the experimental requirements, absorb appropriate amount of bacterial liquid for plasmid extraction.

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