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I use sigma plot software, its a radioligand binding assay for determination of Kd values for the Aptamer-protein binding. I use one site saturation.
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I have been using illustra microspin G50 columns for getting rid of the unincorporated labeled nucleotides from my sample eDNA. But unfortunately this does not seem to work. I still end up with...
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For example, if we have two proteins, is there any way to detect the binding sites (portion of the molecules) with the highest affinity in silico, before actually performing the experiments?
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Furin is expressed as a proprotein, so i had included a myc tag after its cleavage site on the n terminal position. have confirmed the tag by sequencing. Aptly, i need to see the band on a western...
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