CytoSelect™ 24-well Wound Healing Assay
Specifications | |
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Product Category: | Wound Healing |
Detection Method: | Microscopy |
Product Description
- More consistent results well-to-well compared to homemade scratch assays
- Useful for measuring cell migration, cell proliferation and wound closure
- Inert inserts leave no residues that could impede proliferation or migration of cells
Traditionally scratch assays have been used to study cell migration, cell proliferation and wound healing. However, these assays lack a consistently defined wound gap and can result in high inter-sample variation.
Our CytoSelect™ 24-Well Wound Healing Assay provides a much more consistent method to measure cell migration across a wound field gap in vitro. Proprietary inserts generate a consistent 0.9mm wound gap between the cells. Cells may then be treated or monitored for proliferation or migration across the wound field by imaging samples at fixed time points or by time-lapse microscopy.
Assay Principle
Supporting Data
Fig.2. Percent Closure of MEF/STO Cells. STO cells were tested using the CytoSelect™ 24-Well Wound Healing Assay. Cells were cultured 24 hours until a monolayer formed, at which time the inserts were removed to begin the assay. Cells were monitored under DAPI labeling and cell staining for determining percent closure.
Product Citations
- Chawon Yun, et al. (2017) Mechanistic insight into the effects of Aryl Hydrocarbon Receptor activation on osteogenic differentiation. Bone Reports.
- Duran GE, et al. (2017) Decreased levels of baseline and drug-induced tubulin polymerisation are hallmarks of resistance to taxanes in ovarian cancer cells and are associated with epithelial-to-mesenchymal transition. Br J Cancer. doi: 10.1038/bjc.2017.102.
- Guerra, A.D., et al. (2017) Minocycline enhances the mesenchymal stromal/stem cell pro-healing phenotype in triple antimicrobial-loaded hydrogels. Acta Biomater. doi: 10.1016/j.actbio.2017.01.021.
- Kang, H.,et al. (2017) Puerarin inhibits M2 polarization and metastasis of tumor-associated macrophages from NSCLC xenograft model via inactivating MEK/ERK 1/2 pathway. International Journal of Oncology.
- Knudson KM, et al. (2017) NFκB-Pim-1-Eomesodermin axis is critical for maintaining CD8 T-cell memory quality. Proc Natl Acad Sci U S A. doi: 10.1073/pnas.1608448114.
- Catalog Number
CBA-120-CB - Supplier
Cell Biolabs - Size
- Shipping
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