<?xml version="1.0" encoding="utf-8" standalone="yes"?><rss version="2.0" xmlns:atom="http://www.w3.org/2005/Atom"><channel><title>&lt;YOUR NAME HERE&gt; — HTBAA Fall 2026 :: jennifer-zayetsy-almeyda-tejada-almeyda</title><link>https://pages.htgaa.org/2026b/jennifer-zayetsy-almeyda-tejada-almeyda/index.html</link><description>About me Contact info Homework, Labs, and Projects See the nav bar on the left to look through my work for How To Biomanufacture Almost Anything (Fall 2026)!</description><generator>Hugo</generator><language>en</language><atom:link href="https://pages.htgaa.org/2026b/jennifer-zayetsy-almeyda-tejada-almeyda/index.xml" rel="self" type="application/rss+xml"/><item><title>Week 1 HW: Final Project Ideas</title><link>https://pages.htgaa.org/2026b/jennifer-zayetsy-almeyda-tejada-almeyda/week-01-hw-project-ideas/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-01-hw-project-ideas/index.html</guid><description>AI-guided dynamic engineering of CHO cells for bispecific antibody biomanufacturing Jennifer Zayetsy Almeyda Tejada&#10;1. What would I like to biomanufacture and why? My interest in biomanufacturing comes from both my personal experiences and my previous work with cell-based therapies. During college, I became interested in gene therapies, immunotherapies, and the possibility of engineering cells for therapeutic purposes. I later worked at V&amp;C Biotech in Peru, a biotechnology company developing cell-based regenerative therapies, including applications for burn injuries. I was responsible for research and development, which gave me a lot of independence but also made me realize how much more I wanted to learn. Beyond developing the research itself, I became familiar with some of the requirements involved in producing cell-based therapies under controlled conditions, including clean-room environments and standardized manufacturing processes.</description></item><item><title>Week 3 HW: Cell-Free Reaction Design</title><link>https://pages.htgaa.org/2026b/jennifer-zayetsy-almeyda-tejada-almeyda/week-03-cell-free-reaction-design/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-03-cell-free-reaction-design/index.html</guid><description>Literature-guided design and optimization of cell-free reaction formulations Jennifer Zayetsy Almeyda Tejada&#10;1. Objective The goal of this project is to design 20-µL cell-free protein synthesis (CFPS) reactions for sfGFP, PETase/TfCut2, and Reteplase that reduce reagent cost while maintaining or improving production of functional protein. The three targets provide an increasing challenge in folding: sfGFP is a robust reporter with no disulfide bond, TfCut2 contains one disulfide bond, and Reteplase contains nine disulfide bonds and therefore requires substantially stronger control of the oxidative folding environment.</description></item><item><title>Final Project</title><link>https://pages.htgaa.org/2026b/jennifer-zayetsy-almeyda-tejada-almeyda/final-project/index.html</link><pubDate>Mon, 01 Jan 0001 00:00:00 +0000</pubDate><guid>https://pages.htgaa.org/2026b/jennifer-zayetsy-almeyda-tejada-almeyda/final-project/index.html</guid><description/></item><item><title>Week-02-Hw-Dna-Designs</title><link>https://pages.htgaa.org/2026b/jennifer-zayetsy-almeyda-tejada-almeyda/week-02-hw-dna-design/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/index.html</guid><description/></item></channel></rss>