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We examined the effect of ROCK inhibitors (Y-27632, ROCK-1 and ROCK-2 siRNA) on Y79 cell adhesive capacity by cell adhesion assay.
Cell-substrate interactions were examined through cell adhesion assay.
For cell adhesion assay, MS1 cells were deprived of serum for 8 h, seeded to 0.02% Collagen I coated wells, and incubated for 30 min.
To demonstrate the effects of ER-464195-01 on functions of activated leukocytes, we performed the cell adhesion assay in vitro.
The cell adhesion assay showed that both surfaces of the membrane responded well to the cells.
In a cell adhesion assay, the adhesion of fibroblasts to atragin was mediated by αvβ3 integrin.
We have modified cell adhesion assay techniques5,11 to provide a sensitive measure of cell substrate adhesion for both wild-type and variant HTC cells in the presence and absence of serum and plasminogen.
In this series of compound 2, 2a exhibited strong inhibitory activity in in vitro P-selectin mediated cell adhesion assay.
A cell adhesion assay showed that the stimulation of IECs with SCF increased the number of cells adhering to FN.
An in vitro cell adhesion assay on αvβ3-positive U87MG and SCCVII cells demonstrated the high binding affinity of conjugates to integrin αvβ3 (IC50 = 0.19 2.66 μM).
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Cell adhesion assays were performed using Vybrant Cell Adhesion Assay Kit (Molecular Probes) in fibronectin (7 μg/cm) coated 96-well culture plates as per recommended protocol.
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