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We then assessed EPC migration using a transwell assay.
Migration activities of Treg subsets were assessed by using a transwell assay as previously described [26].
Purified KSL cells were isolated from whole bone marrow by cell sorting (≥99% purity), and migration to CXCL12 assessed using a Transwell assay.
Using a transwell assay, migration of osteoclasts was evaluated as described previously with minor modifications [ 41].
Next, the ability to invade Matrigel was assessed using a Transwell assay.
Cell lines were tested for in vitro invasion using a Transwell assay.
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Next, we used a Transwell assay to investigate the role of COMT in tumor cell invasion.
In order to determine the effect of PROKR2 loss upon Prok2 chemoattraction for SVZ progenitor cells, we used a transwell assay.
To compare the motility of HCT116 and p300− cells we used a transwell assay with type-I collagen or matrigel-coated membranes.
To further measure the effect of YL529 on HLECs invasion, we used a transwell assay and measured the number of HLECs that passed through a membrane barrier following treatment with various concentrations of YL529 [ 29].
Cell migration and invasion were gauged using a Transwell migration assay and a Matrigel invasion assay (8 μm pore size; BD Falcon, San Jose, CA, USA) as previously described.
More suggestions(15)
using a transwell system
using a transwell invasion
using a transwell chamber
using a transwell co-culture
using a transwell insert
using a transwell chemotaxis
using a transwell plate
using a transwell filter
using a transwell membrane
using a plate assay
using a glucose assay
using a fluorescence assay
using a bioluminescence assay
using a scratch assay
using a pcr assay
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