Streptococcus suis Transformation: Difference between revisions
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PreDec2022>EricMiller (Created page with "Day 1: *Plate strains from freezer onto Tryptic Soy Plates for single colonies. Day 2: *Put 3ml of Todd-Hewitt + 0.5% Yeast Extract into sterile 16mm test tubes. Add a single...") |
PreDec2022>EricMiller No edit summary |
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Day 3: | Day 3: | ||
#Put 5ml of Todd-Hewitt + 0.5% Yeast Extract into sterile 16mm test tubes to pre-warm the media for 1 hour. | |||
#Add 125 ul of the overnight growth (a 1:40 ratio). | |||
#Allow to grow to an Absorbance of 0.035 - 0.058 (one hour, generally). | |||
#Put 100ul of this culture into a micro-centrifuge tube. | |||
#Add in the correct XIP peptide from the stock to create a final concentration of 250uM. (normally, 7-10ul of stock peptide) | |||
#Add 1.2 ug DNA | |||
#Vortex; place in 37 degree incubator for 2 hours. | |||
#Plate onto appropriate antibiotic plates. |
Revision as of 11:42, 31 July 2019
Day 1:
- Plate strains from freezer onto Tryptic Soy Plates for single colonies.
Day 2:
- Put 3ml of Todd-Hewitt + 0.5% Yeast Extract into sterile 16mm test tubes. Add a single colony into the tube; grow overnight at 37 degrees in the plate incubator (so, without shaking).
Day 3:
- Put 5ml of Todd-Hewitt + 0.5% Yeast Extract into sterile 16mm test tubes to pre-warm the media for 1 hour.
- Add 125 ul of the overnight growth (a 1:40 ratio).
- Allow to grow to an Absorbance of 0.035 - 0.058 (one hour, generally).
- Put 100ul of this culture into a micro-centrifuge tube.
- Add in the correct XIP peptide from the stock to create a final concentration of 250uM. (normally, 7-10ul of stock peptide)
- Add 1.2 ug DNA
- Vortex; place in 37 degree incubator for 2 hours.
- Plate onto appropriate antibiotic plates.