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I want to couple the polypeptide to a cell culture plate, is it easier to couple the polypeptide after a few days of dissolution in PBS?
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Do embryonic stem cells or iPSCs cultured in vitro on normal culture plates migrate spontaneously without any stimulation?
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The amount of total RNA used by each group was different during reverse transcription. Can it be compensated by adjusting the same CT value during PCR?
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Why did someone average the control? When selecting your calibrator sample you can select just one of the ‘controls’ that way only 1 sample in the experiment will have a 2^-ddCT of 1.I see a lot...
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There are binding sites in the receptor, so do ligands have binding sites? Can you give me an example where the ligand is a protein?
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If I isolate a motif in a domain, is it still functional? Will the amino acid sequence function if I synthesize only the binding site region of the domain?
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