Freimoser:Fast yeast transformation protocol - source code
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#include "BioCoder.h"
void main()
{
start_protocol("Freimoser - Fast Yeast Transformation");
Fluid plasmid = new_fluid("DNA plasmid");
Fluid carrier_dna = new_fluid("carrier DNA","salmon/herring sperm DNA in H2O, 2mg/ml stock, 500 µl aliquots, heat-inactivated at 95°C for 5-6 min and put on ice before use (has to be done once)");
Fluid peg = new_fluid("50% polyethylene glycol (PEG) solution", "MW 3'350, filter-sterilized");
Fluid liac = new_fluid("1 M lithium acetate", "autoclaved");
Fluid water = new_fluid("water");
Solid cells = new_solid("cells scrapped from plate");
Plate plate1 = new_plate("plate containing appropriate medium");
Container tube1 = new_container(STERILE_MICROFUGE_TUBE);
//1. Add 50 µl carrier DNA to a 1.5 ml tube.
first_step();
measure_fluid(carrier_dna, vol(50, UL), tube1);
//2. scrap cells from plate and add to the carrier DNA.
next_step();
measure_solid(cells, tube1);
//3. Add in the following order:
//1. 1-2 µl DNA-plasmid (up to 30-50 µl)
//2. 240 µl PEG (50%)
//3. 36 µl Li-Ac (1M)
next_step();
measure_fluid(plasmid, vol_range(1, 2, UL), tube1);
measure_fluid(peg, vol(240, UL), tube1);
measure_fluid(liac, vol(36, UL), tube1);
//4. resuspend with blue tip
next_step();
pipet(tube1);
//5. incubate at 30°C or RT at least 30 min
next_step();
first_option();
incubate(tube1, 30, min_time(30, MINS));
next_option();
incubate(tube1, RT, min_time(30, MINS));
end_option();
//6. heat shock: 45°C, 15 min (or 42°C for 20 min)
next_step("Heat shock");
first_option();
store_for(tube1, 45, time(15, MINS));
next_option();
store_for(tube1, 42, time(20, MINS));
end_option();
//7. spin down, resuspend in 100μl H2O and plate everything on corresponding medium
next_step();
centrifuge_pellet(tube1, speed(SPEED_MAX, RPM), RT, time(1, MINS));
measure_fluid(water, vol(100, UL), tube1);
resuspend(tube1);
name_sample(tube1, "suspension");
plate_out(plate1, tube1);
end_protocol();
}