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At the moment, I'm struggling with a very basic technique. I want to run proteins from lysed T-REx HEK293 cells on a SDS gel. However, instead of sharp protein bands I just see a smear after...
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I have constructed two versions of my GOI with and without a FLAG tag and cloned them into the same vector. However, when I transfect HEK293 cells with my two different constructs, I can detect my...
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