Sickle Cell Anemia is a common genetic disease that causes long rods in red blood cells, giving them a "sickled" appearance. These cells get stuck in small capillaries of the blood stream leading to oxygen deprivation that causes pain and organ damage. Sickle Cell Anemia is caused by a single point mutation in the hemoglobin gene that results in a faulty protein. In this experiment, your students will investigate the restriction enzyme that discriminates between HbA (normal) and HbS (disease) genes and perform a simulated test on a patient.
Discover how a single nucleotide mutation can profoundly affect a person's health
Explore Mendelian genetics and the molecule methods used to identify sickle cell disease
Perform agarose gel electrophoresis to separate differently-sized DNA molecules
Load, run, analyze, and size control samples and samples from a family of three to identify mutations in their hemoglobin genes
Group Size:
For 8 Gels
Time Required:
Complete in 45 minutes
Kit Includes:
Instructions, Ready-to-Load QuickStrip DNA Samples, UltraSpec-Agarose, Electrophoresis Buffer (50X), Practice Gel Loading Solution, FlashBlue DNA Stain.
All You Need:
DNA Electrophoresis, Micropipettes: 5-50 µl (Optional), White Light Box, & Microwave or Hot Plate.
Storage:
Room Temperature Stable. Storage of Ready-to-Load QuickStrip samples in the Refrigerator is Recommended.