Bring non-Mendelian inheritance into your classroom with the Hemophilia Genetic Testing Lab
Uncover the power of genetic testing through a hands-on classroom experience designed to bring non-Mendelian inheritance to life.
In this lab, your students step into the role of a physician treating baby Andrew, a newborn recently diagnosed with hemophilia A, an X-linked bleeding disorder caused by a mutation in the F8 gene. Their mission? To determine whether Andrew’s close female relatives are carriers of the same mutation.
Tap into their diagnostic interests in human diseases and genetic testing with our newest DNA electrophoresis lab, the Hemophilia Genetic Testing: X-linked Inheritance Learning Lab. This lab includes:
- Practical, Hands-On Learning: Students run samples using gel electrophoresis to detect the presence or absence of the F8 deletion in DNA samples. They’ll see real results—right before their eyes.
- Real-World Context: By adopting the mindset of a clinician, students connect foundational genetics concepts to tangible medical scenarios. It’s genetics education with real stakes and meaning.
- Genetic Testing in Action: Students examine inheritance patterns through Punnett squares, pedigrees, and interpreting carrier status, engaging students in X-linked transmission dynamics.
This lab was designed with teachers in mind. Everything, from setup instructions to expected results and teaching resources, is classroom-ready. It’s ideal for high school and undergraduate educators looking to elevate genetics content.
The Hemophilia Genetic Testing: X-linked Inheritance Learning Lab from miniPCR bio bridges the gap between textbook genetics and laboratory science. By empowering students to apply molecular techniques, they learn how to solve diagnostic puzzles, practice critical reasoning, and understand the inheritance of a genetic disease.
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