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I have been trying to process neuronal cells grown as a monolayer on glass coverslips for standard TEM but my images are not to the standard I was hoping for (see attached). It looks to me like...
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I am using real-time PCR to firstly show the presence/absence of certain targets in my tissue and also to then give more information of the relative amounts of these targets compared to each...
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I have loaded my qPCR products onto a 2% agarose gel and ran them at 60V for 1 hour. I ran 2.5ng of cDNA in a 10uL qPCR reaction. As you can see in my image there is smearing of all bands in the...
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