My apologies for perpetually spamming and bumping this thread. One more simplifying idea has occurred to me. Suppose the synthesised TdT enzyme had a long tail at one terminal which was then covalently bound to the glass slide along with the short oligo seeds pre DNA synthesis. No enzyme would then need to be deposed in each new cycle the existing TdT could be reused. Using this system and clearAmp less enzyme would be used and the cheeper four colour epson print heads could be used.
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