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Biocoat matrigel transwell chamber

Manufactured by BD
Sourced in United States

The BIOCOAT Matrigel Transwell chamber is a laboratory equipment used for cell migration and invasion assays. It consists of a porous membrane coated with Matrigel, a basement membrane extract. The chamber allows for the study of cell movement through the membrane, which can be used to evaluate the invasive potential of various cell types.

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2 protocols using biocoat matrigel transwell chamber

1

Matrigel Transwell Invasion Assay

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Cell invasion assay was carried out using BIOCOAT Matrigel Transwell chamber (BD, Franklin Lakes, NJ, USA) with the pore size of 8.0 μm. The inserts were placed into 24-well plates, containing 700 μL of RPMI-1640 medium for 30 minutes in a humidified 37°C incubator under 5% CO2 before seeding cells. After 48 hours transfection, 5×104 cells in each group resuspended in RPMI-1640 medium containing 5% FBS were placed in each chamber. The lower compartment was loaded with full media containing 15% FBS as the nutritional attractant. After being incubated at 37°C for 48 hours, noninvaded cells were scraped off with a cotton swab. The translocated cells on the bottom of upper chamber membrane were fixed with 5% formaldehyde and stained with 1% Giemsa stain. Five fields of fixed cells were randomly chosen and counted under a light microscope.
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2

Transwell Assay for Cell Invasion

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Transwell assays were used to assess cell invasive capacity. Cell invasion assays were carried out using a BioCoat Matrigel Transwell chamber (BD, Franklin Lakes, NJ, USA) with a pore size of 8.0 μm. The inserts were placed in 24-well plates containing 700 μL of DMEM F12 1:1 medium for 30 minutes in a humidified 37 °C incubator under 5% CO2 before seeding the cells. GANT61 (30 umol/L) was used to block the SHH signaling pathway, and after 48 hours, 5 × 104 cells in each group resuspended in DMEM F12 1:1 medium containing 5% FBS were placed in each chamber. The lower compartment was loaded with full media containing 15% FBS as the nutritional attractant. After incubated at 37 °C for 48 hours, noninvaded cells were scraped off with a cotton swab. The translocated cells on the bottom of the upper chamber membrane were fixed with 5% formaldehyde and stained with 1% Giemsa stain. The number of cells that penetrated the upper compartment of the Transwell chamber was determined under an inverted microscope. Five fields of fixed cells were randomly chosen and counted under a light microscope [19 (link)].
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