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大腸桿菌 JM101菌株/感受態(tài)細(xì)胞
NTCC-JM101 | E. coli JM101 | E. coli JM101 strain,500uL, Storage:4℃ |
Description:
Asuspension of E. coli K12 JM101 which has been grown in minimal media and broughtto 50% glycerol.
Genotype:
F′traD36 proA+B+lacIqΔ(lacZ)M15/Δ(lac-proAB) glnV thi
Notes:
Storage at–70°C is recommended for periods longer than 30 days. Avoid repeated freeze/thawcycles.
References:
1. Messing, J. (1979) A multipurpose cloningsystem based on the single-stranded DNA bacteriophage M13, in Recombinant DNA TechnicalBulletin (NIH) Volume 3, Number 2.
2. Yanish-Perron et al. (1985) Gene33,103–119.
Recovery
Obtain an LB agar plate with the appropriate antibiotic.
Using a sterile pipette tip, touch the bacteria growing within the punctured area of the stab culture. (A sterilized wire loop or sterile toothpick can be used in place of a sterile pipette tip.)
Run this tip lightly over a section of the plate, as shown in the figure, to create streak #1.
Using another sterile pipette tip, pass through streak #1 and spread the bacteria over a second section of the plate, to create streak #2.
Using a third sterile pipette tip, pass through streak #2 and spread the bacteria over the last section of the plate, to create streak #3.
Grow overnight in a 37 o C incubator (unless a different growth temperature is indicated on the plasmid datasheet).
In the morning, single colonies should be visible. If the bacterial growth is too dense, re-streak onto a new agar plate to obtain single colonies.
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