pGLO Observations , Data Recording & Analysis
1.
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Obtain your team plates. Observe your set of “+pGLO” plates under room light and with UV light. Record numbers of colonies and color of colonies. Fill in the table below.
Plate
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Number of Colonies
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Color of colonies under room light
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Color of colonies under UV light
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- pGLO LB
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0
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Opaque white
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white
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+ pGLO LB/amp
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Around 50
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Opaque white
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white
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+ pGLO LB/amp/ara
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Around 75
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Opaque white
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Glowing green
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2.
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What two new traits do your transformed bacteria have?
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3.
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Estimate how many bacteria were in the 100 uL of bacteria that you spread on each plate. Explain your logic.
In the 100 uL of bacteria, I estimate that there were about 50-80 bacteria. This is because a colony is one bacteria that split up to form more, so if you count the colonies then you will get an estimate on how many bacteria there are.
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4.
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What is the role of arabinose in the plates?
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5.
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List and briefly explain three current uses for GFP (green fluorescent protein) in research or applied science.
3 current uses for GFP in research or applied science is they can be applied to cancer cells, so doctors can track and observe the cancer cells for developing a cure or just for research. The second reason that I found is scientists attach GFP to insulin producing cells for diabetic research. Another way GFP is used is to track the spread of diseases like HIV.
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6.
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Give an example of another application of genetic engineering.
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