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Exact(5)
We also measured cell migration speed as a function of fibronectin coating concentration at pH 6.5 and pH 7.4.
We initially measured cell migration on fibronectin using the 'scratch assay' under a range of ML-7 concentrations within the culture medium containing saturating levels of EGF.
To investigate whether the observed increase in WNT genes correlates with an EMT-like, migratory and invasive phenotype, we measured cell migration and invasion using live-cell imaging and a quantitative matrix invasion assays.
Hence, we measured cell migration by means of an in vitro scratch assay and proliferation in Hs578T and BT-20 breast cancer and HOC-7 ovarian cancer wild-type cells, CHAC1 knockdown cells and cells treated with a scrbl siRNA as negative control.
To test this hypothesis, we performed TDP-43 knockdown on H1299 lung cancer cells and measured cell migration using the transwell migration assay.
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Modified Boyden chamber assays were performed to measure cell migration.
We applied this technique to measure cell migration in tissue.
Wound healing assays were used to measure cell migration.
Transwell migration assay (Millipore, USA) was used to measure cell migration and invasion capacity in vitro.
We also used an in vitro wound healing assay to measure cell migration (data not shown).
The wound healing and transwell assays directly measure cell migration, an ubiquitous process during embryogenesis and cancer formation.
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assess cell migration
measured cell cycle
measured cell area
measured cell suspension
measured cell motility
measured cell viability
measured cell proliferation
measured cell toxicity
measured cell growth
measured cell adhesion
measured cell number
measured cell death
measured cell potential
measured cell length
measured cell size
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