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Escherichia coli DH5α(pUCGm)
Storage conditions : 2~8 ℃
No. : 357456
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:BNCC354363 pUCGm (containing ampicillin resistance gene).
Medium:LB resistant agar medium yeast extract 5.0g, peptone 10.0g,NaCl 10.0g, agar 15.0g (not included in liquid medium), distilled water 1.0 L,pH 7.0. Sterilization at 121 ℃ for 15min. After sterilization, add ampicillin sodium after cooling and cooling, so that the final content of ampicillin sodium in the culture medium is 50 μg/mL. Culture 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, 200μL/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.
Plasmid purification:
1. pick a single colony and inoculate it into 50mL liquid LB resistance medium, and culture at 37 ℃ overnight;
2. according to the experimental requirements, absorb appropriate amount of bacterial liquid for plasmid extraction. Blank control LB resistant plate screening results