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Transwell filter system

Manufactured by Corning
Sourced in United States

The Transwell filter system is a laboratory equipment used for cell culture applications. It consists of a permeable membrane insert placed in a well of a multi-well plate, allowing for the separation of different cell types or the study of cell migration and permeability. The system facilitates the exchange of media, nutrients, and signaling molecules between the upper and lower chambers.

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Lab products found in correlation

2 protocols using transwell filter system

1

Transwell and Scratch Assays for Cell Migration

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Cell migration was measured by a Transwell filter system (Corning-Costar, New York, US) with a filter with 8 µm pores. After culture in serum-free medium for 24 h, the cells (2×105 cells/well, 300 µL) of the different groups were seeded into the upper chamber of the insert, and a complete medium (700 µL) was added to the lower chamber. The Transwell filter systems were then incubated for 72 h at 37°C with 5% CO2. The cells were fixed with methanol (Sinpharm, Beijing, China), and the cells that remained on the upper surface of the filter were removed carefully with a cotton swab. The cells were stained with 0.5% crystal violet (Solarbio, Beijing, China) for 30 mins and counted under a microscope (Caikon, Shanghai, China).
Cell scratch test can also be used to examine cell migration. After culture for 24 h, the cells (8×105 cells/well) of the different groups were seeded into the culture medium. A 10 µL pipette tip was used to draw a line in the middle of the dish, and the cells were cultured in an incubator for 24 h. Pictures of the scratches were taken at 0 h and 24 h.
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2

Chemotaxis Assay for Primary Human PMNs

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Chemotaxis of primary human PMNs was assessed in 24-well plates using a 3 μm-pore size Transwell filter system (Costar, Cambridge, MA). Migration buffer (400 μl) containing the indicated chemoattractants or conditioned media was added to the lower chamber and PMNs were loaded onto the inserts at a density of 1 × 106 cells/100 μl. The cells were then allowed to migrate for 2 hours at 37°C. Following incubations, 40 μl of 0.5 M EDTA was added to the lower chamber and the plate was incubated for 15 min at 4°C. The number of cells in the lower chamber was counted using a hemocytometer and the percentage of migrating cells was determined.
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