Using CRISPR to treat cystic fibrosis

Supplier: EDVOTEK
135
EDVO135EA 110 GBP
EDVO135
Using CRISPR to treat cystic fibrosis
Educational Materials Biology Educational Materials Genetics Learning Activities
Hands-on simulation of CRISPR-Cas9 to target and treat Cystic Fibrosis.

  • Teach your students about new CRISPR technology
  • Includes all required reagents
  • Use DNA electrophoresis to view reach a diagnosis.
  • Activity can be completed in 45 minutes

In this experiment, students will simulate the use of CRISPR-Cas9 to target a genetic mutation found in a patient suffering from Cystic Fibrosis.

Students will develop an understanding of guide RNA (gRNA) design, and use agarose gel electrophoresis to examine pre-prepared DNA samples after CRISPR treatment.

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