We report a fabrication method of a "post-molecule/cell patterned" glass microchip using pressure-based low/room temperature bonding in dry conditions combined with fluorosilane patterning. Multiple proteins/cells were patterned in a single channel using this method. This simple method will provide benefits for using microchips for high throughput analysis in many biological experiments.
No takes yet. Share an insight, caveat, or question.
Funano et al. (2017) studied this question.
Synapse has enriched 4 closely related papers on similar clinical questions. Consider them for comparative context: