Teaching Microfluidic Diagnostics Using Jell-O® Chips

  • Cheng Wei T. Yang
  • Eric T. LagallyEmail author
Part of the Methods in Molecular Biology book series (MIMB, volume 949)


Microfluidics has emerged as a versatile technology that has found many applications, including DNA chips, fuel cells, and diagnostics. As the field of microfluidic diagnostics grows, it is important to introduce the principles of this technology to young students and the general public. The objective of this project was to create a simple and effective method that could be used to teach key microfluidics concepts using easily accessible materials. Similar to the poly(dimethylsiloxane) soft lithography technique, a Jell-O® “chip” is produced by pouring a mixture of Jell-O® and gelatine solution into a mold, which is constructed using foam plate, coffee stirrers, and double-sided tape. The plate is transferred to a 4°C refrigerator for curing, and then the Jell-O® chip is peeled off for experimental demonstrations. Three types of chips have been fabricated with different molds: a JELLO mold, a Y-channel mold, and a pH-sensor mold. Using these devices, the basics of microfluidic diagnostics can be demonstrated in one or two class periods. The method described in this chapter provides teachers with a fast and inexpensive way to introduce this technology, and students with a fun and hands-on way to understand the basics of microfluidic diagnostics.

Key words

Microfluidics Microfluidic diagnostics Lab-on-a-chip Microfluidics education Teaching methods Jell-O microfluidics 



Jake Abbot and Cameron Lawson, two Grade-10 high school students from Prince of Wales Mini School in Vancouver (working through a mentorship program at the Michael Smith Laboratories), helped with developing the initial protocol and testing the first Jell-O® chips. An undergraduate student working in our laboratory, Adrian Lee, created new experiments based on their techniques. The authors would like to thank Drs. David Ng and Joanne Fox for the initial idea and the 2009 UBC iGEM Team and Lagally lab members for their technical support. Financial support of this work by the Michael Smith Laboratories’ start-up funding to ETL is gratefully acknowledged.


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Copyright information

© Springer Science+Business Media,LLC 2013

Authors and Affiliations

  1. 1.Michael Smith Laboratories & Department of Chemical and Biological EngineeringUniversity of British ColumbiaVancouverCanada
  2. 2.Michael Smith LaboratoriesUniversity of British ColumbiaVancouverCanada
  3. 3.Department of Chemical and Biological EngineeringUniversity of British ColumbiaVancouverCanada

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