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. 1997 Oct;8(10):1863–1875. doi: 10.1091/mbc.8.10.1863

Figure 3.

Figure 3

α2β1-mediated K562 transfectant cell migration on collagen and laminin upon stimulation by JBS2. Migration of KX2C2 (A and B) and KX2C2(I) (C and D) transfectant cells were carried out on polycarbonate filters (10-μm pore size) coated with collagen (A and C) or laminin (B and D) at 10 μg/ml in the presence of α2β1 stimulatory mAb JBS2 or in combination with 10 mM Mn2+. The role of α2β1 was determined using blocking mAb BHA2.1, with the isotype matched mAb P3 as control. All mAbs were used at 20 μg/ml. Values were enumerated from the average (±SD) of cell counts from five random high-power fields (400×) from a minimum of three independent experiments.