User:Allison K. Alix/Notebook/Thesis Research/2013/04/16: Difference between revisions
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==Procedures== | ==Procedures== | ||
Part one: Reconstituting samples in water | Part one: Reconstituting DNA samples in water | ||
1) Remove epi-test tubes from lyophilizer | 1) Remove epi-test tubes from lyophilizer | ||
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Part 2: Gel Electrophoresis. | Part 2: Gel Electrophoresis. | ||
1) Follow procedure outlined on | 1) Follow procedure outlined on [[User:Allison K. Alix/Notebook/Thesis Research/2013/03/29|03/29/2013]] | ||
2) Prepare the following 7 samples: | |||
54.8micL in 445.2 mic buffer | * 1μL 1kb DNA ladder + 1μL loading dye + 4μL filtered water | ||
* 1μL 100bp DNA ladder + 1μL loading dye + 4μL filtered water | |||
* 1μL thiol-DNA/AuNP + 1μL loading dye + 4μL filtered water | |||
* 1μL supernatant 1 + 1μL loading dye + 4μL filtered water | |||
* 1μL supernatant 2 + 1μL loading dye + 4μL filtered water | |||
* 1μL supernatant 3 + 1μL loading dye + 4μL filtered water | |||
* 1μL supernatant 4 + 1μL loading dye + 4μL filtered water | |||
3) Load into gel | |||
4) Stain with ehtidium bromide | |||
5) Observe under UV Light | |||
Part 3: Preparing thiol-DNA/ThT solution | |||
* Because we are reacting the ThT with the DNA prior to reaction with the gold nanoparticles, it is important to account for an extra dilution that minimizes the concentration of the DNA. We are looking for the DNA to be 75x higher than the concentration of the gold nanoparticles (19.4nM x 74 = 1455nM). In order to have this concentration of DNA by the time it is ready to be mixed with the AuNP, it was calculated that we need to start with a 5.82μM solution | |||
1) Dilute stock DNA (53.1μM) to 5.82μM | |||
53.1μM DNA (x) = (500μL) (5.82μM) | |||
X = 54.8micL in 445.2 mic buffer | |||
2) Mix 250μL thiol-DNA with 250μL 5μMThT | |||
3) Heat at ~75°C for 25 minutes | |||
4) Cool to room temperature | |||
Revision as of 09:36, 16 April 2013
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Objectives
ProceduresPart one: Reconstituting DNA samples in water 1) Remove epi-test tubes from lyophilizer 2) Add 10 μL water to each sample and vortex to dissolve Part 2: Gel Electrophoresis. 1) Follow procedure outlined on 03/29/2013 2) Prepare the following 7 samples:
3) Load into gel 4) Stain with ehtidium bromide 5) Observe under UV Light Part 3: Preparing thiol-DNA/ThT solution
1) Dilute stock DNA (53.1μM) to 5.82μM 53.1μM DNA (x) = (500μL) (5.82μM) X = 54.8micL in 445.2 mic buffer 2) Mix 250μL thiol-DNA with 250μL 5μMThT 3) Heat at ~75°C for 25 minutes 4) Cool to room temperature
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