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Team:WarrenCIndpls IN-HS/Project
From 2011.igem.org
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=== The Experiment === | === The Experiment === | ||
| - | '''DNA Extraction:''' | + | '''''DNA Extraction:''''' |
1) Pipet 200 microliters of distilled water into two centrifuge tubes | 1) Pipet 200 microliters of distilled water into two centrifuge tubes | ||
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12) Pipet 200 microliters of ethyl alcohol(cold) into each tube and allow seperation to take place for 15 minutes. | 12) Pipet 200 microliters of ethyl alcohol(cold) into each tube and allow seperation to take place for 15 minutes. | ||
| - | '''DNA Amplification (PCR)''' | + | '''''DNA Amplification (PCR)''''' |
1) In each tube, there will be three layers of materials; using the pipet, collect the first and half of the second layers of each tube. | 1) In each tube, there will be three layers of materials; using the pipet, collect the first and half of the second layers of each tube. | ||
Revision as of 04:02, 25 June 2011
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Some bacteria have been genetically modified to detect certain metals in a water supply. However, it has not been done in yeast. If yeast is genetically engineered to do so, it would be a much safer procedure. The objective for was to create a bio-brick. The creation of the part will enable next year's team to complete the overall goal, which is to create and insert a plasmid into yeast that will cause it to glow red in the presence of a certain metal. | File:WarrenCIndpls IN-HS team.png Your team picture |
| Home | Team | Official Team Profile | Project | Parts Submitted to the Registry | Modeling | Notebook | Safety | Attributions |
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Contents |
Overall project
Project Details
Gibson Assembly
The Experiment
DNA Extraction:
1) Pipet 200 microliters of distilled water into two centrifuge tubes
2) Add a drop of detergent to each tube and shake.
3) Label the tubes according to what will go into each.
4) Rub the loop end of the inoculating loop across the surface of the agar with the E.Coli containing the ADH terminator.
5) Place the loop into the corresponding tube and swivel the loop a few times.
6) Repeat 4-5 with the E.Coli containing M-Cherry.
7) Shake the tubes well or place them on a vortex.
8) Place in a hot water bath at 56-60 degrees Celsius for 10 minutes
9) Add a pinch of meat tenderizer to each tube. -this will break apart the proteins holding the cells together.
10) Vortex the solutions again.
11) Place them in a water bath at 56-60 degrees Celsius for 20 minutes
12) Pipet 200 microliters of ethyl alcohol(cold) into each tube and allow seperation to take place for 15 minutes.
DNA Amplification (PCR)
1) In each tube, there will be three layers of materials; using the pipet, collect the first and half of the second layers of each tube.
2) Place the collected material into a different centrifuge tube each. (Label)
3) Spin both tubes down using the centrifuge.
4) Pour off the supernatants.
5) Resuspend the DNA pellets in each tube by adding 200 microliters
6)
