JM110 E. coli|BNCC357910 |BNCC

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JM110 E. coli

Culture medium	Base medium (English name: LB): yeast extract 5.0g, peptone 10.0g,NaCl 10.0g, distilled water 1.0L,pH 7.0. Sterilization at 121 ℃ for 15min.
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 ℃
Sharing mode	Public welfare sharing

Escherichia coli JM110

Storage conditions : 2~8 ℃

No. : 357910

Product format :freeze dried, 200ul

Validity : 6 years

Biosafety level : 1, handle in ultra-clean table or safety cabinet

Uses : competent cells, plasmids, genetic engineering

* Note : This product is transported at room temperature. Please store it at 2-8 ℃ after receiving it. If any abnormal situation such as damage is found on the same day, please contact customer service within 24 hours. The freeze-dried powder shall be used up once after being opened and shall not be retained. Please operate in strict accordance with this instruction, otherwise the replacement service will not be provided if the strain is abnormal and inactivated.

Medium :LB agar medium yeast extract 5.0g, peptone 10.0g,NaCl 10.0g, agar 15.0g, distilled water 1.0 L,pH 7.0. Sterilization at 121 ℃ for 15min.

Growth conditions

Temperature :37 ℃

Gas environment : Aerobic

How to use
A. Recovery
1. Prepare 2 LB plates;
2. under sterile conditions, draw 0.5mL of liquid culture medium into a lyophilized tube to fully dissolve the freeze dried pellets;
3.inoculate two plates with the liquid suspension, and streak the two plates, in 18-24h a single colony grow ;

B. Competent preparation (for reference)
1. inoculate a test tube of 3ml LB liquid medium with a single colony from JM110(DE3) E. coli plate , and put the test tube on a shaker at 37 ℃ overnight.
2. take 1ml of bacterial solution and transfer it to a conical flask containing 50ml LB liquid culture medium. shake culture at 37 ℃ for 2~3h, A600 should be between 0.4~0.5, and the number of cells must be <108CFU/ml.
3. transfer 1ml of bacterial liquid to a 1.5 ml centrifuge tube with a pipette and place it on ice for 10min.
4. Centrifugation for 10min,4000r /min.
5. suck out all the supernatant and add 200ul of ice-cold CaCl ( 0.1mol/l), then immediately place on ice for 30min.
6. low temperature centrifugation for 10min,4000r /min to collect cells.
7. suspend the cells with 200ul of ice-cold CaCl ( 0.1mol/l).
8. sub-package cells, each 200ul, this is competent cells.

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