QCM Chemotaxis Cell Migration Assays
- Quantitative fluorescent method increases sensitivity 10-fold over similar assays on the market
- Does not require cell pre-labeling, cell scraping, or cell counting
- Results in 4–24 hours
- 96-well plate is ideal for high throughput screening
QCM Chemotaxis Cell Migration Assays are built on the platform of a multiwell plate that includes a 24- or 96-well migration chamber and a feeder tray. Each chamber contains a microporous polycarbonate membrane of a specified pore size. Both sides of the membrane are uncoated. Cells of interest are pipetted onto the top of the insert. Migratory cells move through the pores of the membrane and cling to the bottom of the polycarbonate membrane, in response to a chemoattractant loaded into the bottom feeder tray.
Fluorescent Assays
Migrated cells are detached, lysed, and labeled with a fluorescent dye that exhibits strong fluorescence when bound to cellular nucleic acids. Sample fluorescence is measured with a fluorescence microplate reader. The excitation maximum is 480 nm; the emission maximum is 520 nm.
Colorimetric Assays
Migrated cells on the bottom of the plate are stained and either viewed with a light microscope or extracted and detected on a standard microplate reader (560 nm).
Pore Size Options
8 µm – suitable for fibroblasts, endothelial cells
5 µm – suitable for monocytes, macrophages
3 µm – suitable for lymphocytes
Human Fibrosarcoma HT-1080 Chemotaxis Assay. HT-1080 Chemotaxis toward 10% FBS was tested in the presence or absence of 10 µm Cytochalasin D. 40,000 cells were used in each assay. Fluorescence measurements were taken at 2, 4, or 24 hours according to assay instructions. |
Kit Components
Colorimetric Assay
- Boyden Chamber Plate Assembly with porous membrane inserts
- Cell Stain Solution
- Extraction Buffer
Fluorimetric Assay
- Boyden Chamber Plate Assembly with porous membrane inserts
- Cell Detachment Buffer
- Lysis Buffer
- CyQuant® GR Dye
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