Cell Invasion Assay (Basement Membrane), 96-well, 8 µm (ab235697) uses a Boyden chamber coated with Basement Membrane Extract (BME), where the cells invade the matrix and then migrate through a semi-permeable membrane in the Boyden chamber in response to stimulants or inhibitory compounds.
Fluorescent
Suspension cells, Adherent cells
Mouse, Human
Select an associated product type
Cell Invasion Assay (Basement Membrane), 96-well, 8 µm (ab235697) uses a Boyden chamber coated with Basement Membrane Extract (BME), where the cells invade the matrix and then migrate through a semi-permeable membrane in the Boyden chamber in response to stimulants or inhibitory compounds.
Fluorescent
Suspension cells, Adherent cells
Mouse, Human
Microplate reader
Blue Ice
-20°C
-20°C
-20°C
Cell Invasion Assay (Basement Membrane), 96-well, 8 μm (ab235697) utilizes a Boyden chamber coated with Basement Membrane Extract (BME), where the cells invade the matrix and then migrate through a semi-permeable membrane in the Boyden chamber in response to stimulants or inhibitory compounds. The percent cell invasion can be analyzed directly in a plate reader. Our assay is easy to use, sensitive and adaptable to high-throughput systems.
This product is manufactured by BioVision, an Abcam company and was previously called K912 EZCellTM Cell Invasion Assay (Basement Membrane), 96-well, 8 μm. K912-100 is the same size as the 100 test size of ab235697.
Cell invasion is the ability of cells to migrate from one area to another through an extracellular matrix. Cell invasion is exhibited by both normal cells as well as cancerous cells in response to specific external signals, including chemical & mechanical stimuli. During invasion, extracellular matrix is enzymatically degraded by cellular proteases before cells migrate to the new location. Cell invasion is required for normal processes such as wound repair, vasculature formation and the inflammatory response as well as the abnormal invasion of tissues by tumor cells during metastasis.
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Full details and terms and conditions can be found here:
Terms & Conditions.
Standard Curve.
HT-1080 cells were harvested, counted and serially diluted to obtain desired cell number. Cells were incubated according to the protocol with Cell Invasion Dye and fluorescence (Em/Ex 530/590) was measured.
Cell Invasion.
3T3-NIH and HT-1080 cells were starved overnight and treated with Control Invasion Inducer or remain untreated (No Treatment). Treatment with Control Invasion Inducer demonstrated a significant increase in invasion of HT 1080 cells as compared to 3T3-NIH control cells.
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