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Listen to ibidi’s recorded webinar "Cell Migration, Wound Healing, and Invasion: Performing an Assay and Quantitative Image Analysis".
ibidi FAQs
Find answers to frequently asked questions on wound healing and migration assays.
Comparison to Scratch Assay
The scratch assay is a widely used technique for investigating wound healing processes. After manually scratching the cell surface with a pipet, the generated wound closes by migration and proliferation of the cells.
However, regarding reproducibility, this method has certain drawbacks:
- The gap width is highly dependent on the pressure applied to the pipet tip.
- Scratching removes the surface coating.
- The removed cells form clumps of living and dead cells at the edges of the scratch. The spreading of living cells can overlay the speed of migration.
The Culture-Insert, in combination with the ibiTreat surface of the μ-Dish, overcomes the problems associated with the scratch assay. When the insert is removed there is no change to the ibiTreat surface. This has been proven in tests with different types of cells, such as fibroblasts, keratinocytes, and several endothelial cell types.
ibidi Culture-Inserts | Scratch Assays |
Cell seeding into designated areas | Scratching with a needle or tip |
Defined cell-free gap | Varying cell-free gap – not reproducible |
Defined non-coated surface | Possible extra-cellular matrix remains |
No cell damage | Cell damage |
Internal reference | No internal reference* |

*Internal Reference
The internal reference may answer the question as to whether two opposite cell fronts influence each other or not. With the defined cell seeding technique, it is possible to measure the speed of:
A: a cell front that is opposite another cell front; and
B: a single cell front that does not have an opposite cell front.

