Protocol tips
Upstream tips |
Protocol tips |
Downstream tips |
Store all components at 4ºC and before use allow the invasion chamber plate to warm up at room temperature for 10 minutes. |
Incubate for 72 hours at 37ºC in 5% CO2 atmosphere. |
Measure the OD 570nm in a
plate reader |
Upstream tips |
Store all components at 4ºC and before use allow the invasion chamber plate to warm up at room temperature for 10 minutes. |
Protocol tips |
Incubate for 72 hours at 37ºC in 5% CO2 atmosphere. |
Downstream tips |
Measure the OD 570nm in a
plate reader |
Publication protocol
In vitro cell invasion assay was performed using a basement membrane-coated CytoSelect™ 24-well Cell Invasion Assay Kit (8 mm pores, Colorimetric Format, Cell Biolabs, San Diego, CA, US) according to the manufacturer’s instruction. Briefly, CD10- or mock-A375 cells were serum-starved for 24 h. Next, the cells suspended with serum-free media (3 X 105 cells/well) were seeded in the upper chamber separated from a lower chamber filled with media containing 10% FBS and incubated for 72 h. After noninvasive cells were removed, the invasive cells were stained and quantified by measuring the absorbance at 570 nm using a microplate reader (iMark™ Microplate Absorbance Reader, Bio-Rad Laboratories). All assays were carried out 3 times in triplicates.
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Paper title
CD10-Equipped Melanoma Cells Acquire Highly Potent Tumorigenic Activity: A Plausible Explanation of Their Significance for a Poor Prognosis
Manufacturer protocol
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