This
Friday, September 18th, we analyzed the PCR products in an agarose gel under UV
light in order to asses whether we were ready to continue analyzing field
samples for the presence of Legionella. As you can see in the picture below, we were
unsuccessful since there was a lot of shearing in the gels and we will be
repeating the protocols on the same PCR products next Tuesday. Then next Friday
we plan to repeat PCR in hopes we get better results and can move forward with
the experiment.
Analysis
on Agarose Gel Electrophoresis (9-18-15)
1% Agarose gel with 1μL/1% SYBER®Green.
Loaded:
Molecular Weight Marker (2 μL).
positive control DNA (5 μL)
loading dye (2 μL)
2 μL water
Loaded 7 μL of control DNA sample and 2
μL of molecular weight marker.
Ran gel at 100 volts for 45-50 minutes
in a 1x TAE Buffer solution (490mL dI water +10 mL 50xTAE)
Placed gel in gel doc to analyze banding.
16s control DNA gel
Lane 1
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Lane 2
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Lane 3
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Lane 4
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Lane 5
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Lane 6
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Lane 7
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Lane 8
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MWM
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7-7-15
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7-8-15
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7-13-15
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7-30-15
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Mip control
DNA gel
Lane 1
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Lane 2
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Lane 3
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Lane 4
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Lane 5
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Lane 6
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Lane 7
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Lane 8
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MWM
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7-7-15
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7-8-15
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7-13-15
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7-27-15
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