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It looks almost as if the interphase is floating up into the aqueous phase during my extraction procedure. It doesn't form a distinct layer; it is very irregularly shaped and juts out into the...
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I have read somewhere that these should be only taken as a frame of reference? I am assuming that my samples with a 260/280 ratio of ~1.5 are too low, but when I run it on a 1% agarose gel, the...
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I am trying to determine the integrity for RNA-seq. I just ran a normal 1% agarose gel 60V for 1h. The 28S band seems to be a smear for all the samples, even the ones with a good 260/280 ratio of...
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