I ran dna in a 1% agaraose gel and in 1x TAE, i saw a strange blue region somewhere in the middle of the gel. I used ethidium bromide to visualize DNA. what could that blue region be? I tried to move gel around thinking that it may be the UV light that i am using, but that did not change. I even used another UV machine and had same result.
Makes me laugh brother, go read and understand the complexity of the cellular physiology. Putting pile of parts does not make a working machine. Cell is even more complex than that, mentioned earlier cells needs specialized cues to function properly.
Lets say there is a bacteria X with 10 different types of plasmid in it. And i want to isolate each of the plasmid and identify them. How can i isolate each of these 10 plasmid without contamination? Can it be done based on size, Centrifugation based on the kb of the plasmid? I need to know the way to isolate each plasmid separately.
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