<?xml version="1.0" encoding="utf-8" standalone="yes"?><rss version="2.0" xmlns:atom="http://www.w3.org/2005/Atom"><channel><title>Week-02-Hw-Dna-Designs :: jennifer-zayetsy-almeyda-tejada-almeyda</title><link>https://pages.htgaa.org/2026b/jennifer-zayetsy-almeyda-tejada-almeyda/week-02-hw-dna-design/index.html</link><description/><generator>Hugo</generator><language>en</language><atom:link href="https://pages.htgaa.org/2026b/jennifer-zayetsy-almeyda-tejada-almeyda/week-02-hw-dna-design/index.xml" rel="self" type="application/rss+xml"/><item><title>Week 2 HW: DNA Design</title><link>https://pages.htgaa.org/2026b/jennifer-zayetsy-almeyda-tejada-almeyda/week-02-hw-dna-design/hw2_index/index.html</link><pubDate>Mon, 01 Jan 0001 00:00:00 +0000</pubDate><guid>https://pages.htgaa.org/2026b/jennifer-zayetsy-almeyda-tejada-almeyda/week-02-hw-dna-design/hw2_index/index.html</guid><description>Programmable CHO cell-state control for biomanufacturing Jennifer Zayetsy Almeyda Tejada&#10;My project asks whether synthetic gene regulation combined with AI-guided cell-state modeling can be used to program CHO cells to transition from a growth-oriented state to a production-oriented state during biomanufacturing.&#10;For this homework, I reduced the larger project to a smaller and experimentally interpretable proof-of-concept genetic circuit. The current construct uses constitutive expression of rtTA3G together with a TRE3G-controlled XBP1s reporter cassette. Doxycycline provides an external timing input, allowing the production-associated module to be activated at a selected point during culture.</description></item></channel></rss>