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. Author manuscript; available in PMC: 2013 Oct 21.
Published in final edited form as: Lab Chip. 2012 Oct 21;12(20):4120–4127. doi: 10.1039/c2lc40315c

Scheme 2.

Scheme 2

Process flow for surface patterning of biomolecules and bonding. The stamp is first inked with 1 mg/mL BSA-biotin solution (ii), dried with nitrogen and stamped onto a pristine glass slide with finger pressure (iii). The pattern is then incubated with a 5% (wt/v) BSA solution in phosphate-buffered saline (PBS) for 15 minutes for blocking, followed by a droplet of 1 mg/mL streptavidin and then 100 nM biotin-modified Kras-capturing DNA for 1 hour and overnight, respectively. The patterned substrate is then bonded to a PDMS chamber that has either been activated by oxygen plasma, or polymer-grafted and hydrolyzed. After a 4-hour baking step, the Cy5-labeled DNA target oligonucleotides are introduced and DNA capture is observed under fluorescence scanner