<?xml version="1.0" encoding="utf-8" standalone="yes"?><rss version="2.0" xmlns:atom="http://www.w3.org/2005/Atom"><channel><title>Microfluidics on Fondsites</title><link>https://fondsites.com/tags/microfluidics/</link><description>Recent content in Microfluidics on Fondsites</description><generator>Hugo</generator><language>en-us</language><lastBuildDate>Fri, 29 May 2026 13:43:57 +0300</lastBuildDate><atom:link href="https://fondsites.com/tags/microfluidics/feed.xml" rel="self" type="application/rss+xml"/><item><title>Microfluidics for Synthetic Biology Screening: Small Channels, Better Questions</title><link>https://fondsites.com/synthetic-biology/guidebooks/microfluidics-synthetic-biology-screening/</link><pubDate>Fri, 29 May 2026 00:00:00 +0000</pubDate><guid>https://fondsites.com/synthetic-biology/guidebooks/microfluidics-synthetic-biology-screening/</guid><description>&lt;p&gt;Microfluidics makes synthetic biology feel smaller and faster, but its real value is not the tiny scale itself. It is the way small volumes can turn a biological question into many careful comparisons. A channel on a chip can hold a stream of cells, droplets, extracts, reagents, or samples in a form that is easier to handle in large numbers. A droplet can become a miniature test chamber. A patterned surface can expose cells to a controlled gradient. A small reaction can conserve material while making it possible to compare many designs side by side.&lt;/p&gt;</description></item></channel></rss>