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Synthetic Biology | Virtual Lab

Higher Education
Biology
Health Sciences
Chemistry
Health Sciences
Synthetic Biology
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About This Simulation

Join cutting edge research at MIT and design a biological circuit that can sense and destroy cancer cells.

Learning Objectives

  • Engineer natural systems to perform specific functions
  • Describe the fundamentals of the Gateway cloning technique and design your own biological circuit
  • Explain and perform bacterial transformation, antibiotic selection and plasmid purification
  • Explain and perform a restriction digest of your cloning product

About This Simulation

Level:
Higher Education
Length:
62
Min
Accessibility Mode:
Available
Languages:
English
Italian
Spanish
German
French

Lab Techniques

  • Gel electrophoresis
  • Restriction digest
  • Electroporation
  • Antibiotics selection
  • Plasmid isolation with purification columns
  • Gateway cloning technique
  • Sterile technique
No lab techniques are listed for this simulation.

Related Standards

University:
NGSS:
  • No direct alignment
AP:
  • No direct alignment
LB:
  • No direct alignment
No lab techniques are listed for this simulation.

Learn More About This Simulation

Use the specific microRNA profile of cancer cells to design an apoptotic biological circuit that is only activated in cancer cells. You are the only hope for a patient with a rare form of cancer.

Learn how to use the Gateway cloning technique

In the Synthetic Biology simulation, you will learn how to use the Gateway cloning technique to combine different genetic modules in an expression vector. You will learn how the Gateway cloning technique can be used to efficiently combine these modules. Use electroporation to transform the bacteria with your vector of interest and select successful transformants. You will learn all about the basics of sterile lab work and bacterial selection.

Extract and isolate plasmids

Your next task in the lab will be to grow the transformed bacteria and extract the plasmids using a ‘miniprep’ kit. You will learn how different buffers enable you to isolate plasmid, and not genomic, DNA from the cells. You will check if the plasmid, indeed, contains your circuit, and if it is mutation-free by digesting it with restriction enzymes and by using gel electrophoresis. In the end you will test your circuit in living cells to see if the cancer cells are the only cells that die.

Will you be able to find a cure for this rare form of cancer?

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