I am working on developing 3D cell cultures of tumor cells and I noticed that there are different methods, like liquid overlay, air interface culture, hanging drop technique, and scaffold-mediated approaches.

As for the liquid overlay approach, the general idea is to create a surface that cells cannot adhere onto. I am curious about whether I can use matrigel to replace agar/agarose or HEMA for the development of 3D cell culture?

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