<?xml version="1.0" encoding="utf-8" standalone="yes"?><rss version="2.0" xmlns:atom="http://www.w3.org/2005/Atom"><channel><title>&lt;GRACIOUS OSAIBHUE ISOAH&gt; — HTBAA Fall 2026 :: gracious-isoah</title><link>https://pages.htgaa.org/2026b/gracious-isoah/index.html</link><description>About me I have a background in microbiology, and I’m deeply interested in biotech entrepreneurship and venture building. I believe biotechnology can be a powerful tool for solving real problems across Africa, and I’m currently building the knowledge, skills, and experience I need to launch a biomanufacturing venture here on the continent.</description><generator>Hugo</generator><language>en</language><atom:link href="https://pages.htgaa.org/2026b/gracious-isoah/index.xml" rel="self" type="application/rss+xml"/><item><title>Week 1 HW: Final Project Ideas</title><link>https://pages.htgaa.org/2026b/gracious-isoah/week-01-hw-project-ideas/index.html</link><pubDate>Mon, 01 Jan 0001 00:00:00 +0000</pubDate><guid>https://pages.htgaa.org/2026b/gracious-isoah/week-01-hw-project-ideas/index.html</guid><description/></item><item><title>Week 2 HW: DNA DESIGN</title><link>https://pages.htgaa.org/2026b/gracious-isoah/week-02-dna-design/index.html</link><pubDate>Mon, 01 Jan 0001 00:00:00 +0000</pubDate><guid>https://pages.htgaa.org/2026b/gracious-isoah/week-02-dna-design/index.html</guid><description>HTBAA Homework #2: Recombinant Taq DNA Polymerase Expression Construct Part 0: Kernel setup I created the Kernel repository Gracious Osaibhue Isoah and the folder Parts folder for parts and Construct folder for construct in the HTBAA 2026 workspace.&#10;Figure 1. Kernel repository and project folder created for the Taq DNA polymerase expression-construct design.</description></item><item><title>Week 3 HW: CELL FREE PROTEIN SYNTHESIS</title><link>https://pages.htgaa.org/2026b/gracious-isoah/week-03-cfps/index.html</link><pubDate>Mon, 01 Jan 0001 00:00:00 +0000</pubDate><guid>https://pages.htgaa.org/2026b/gracious-isoah/week-03-cfps/index.html</guid><description>A. COMPARE CELL-FREE REACTION COMPOSITIONS Why does the concentration of potassium glutamate and magnesium glutamate differ between compositions? Which is more sensitive? Potassium glutamate and magnesium glutamate are water-soluble ionic salts added to the buffer of cell-free protein synthesis to mimic the cytoplasmic environment of the cell. They provide critical ions like Mg²⁺ and K⁺ at concentrations required for transcription, translation, ribosome function, and energy metabolism. Glutamate is generally a more physiologically suitable counter-anion than chloride for many bacterial CFPS systems. CFPS yields are known to be more sensitive to magnesium glutamate. It provides a more constrained variable, Mg²⁺. In a study by Cai et al., changes of about 1-2 mM in concentration can increase/decrease protein yield. Free Mg²⁺ is a core component of the translation machinery. It stabilizes rRNA and the functional structure of RNA. Other CFPS reagents, including ATP, GTP, and nucleic acids, bind to Mg²⁺ due to its chelating effect.</description></item><item><title>Final Project</title><link>https://pages.htgaa.org/2026b/gracious-isoah/final-project/index.html</link><pubDate>Mon, 01 Jan 0001 00:00:00 +0000</pubDate><guid>https://pages.htgaa.org/2026b/gracious-isoah/final-project/index.html</guid><description/></item></channel></rss>