Fig. 1.
Fig. 1. Rolling flux of CD34+ and CD34− FL cells on P- and L-selectin at a shear rate of 210 s−1. / Cells were subjected to wall shear rates from 487 s−1to 77 s−1 on P- or L-selectin chimeras adsorbed at 2 μg/mL on silanated glass. Rolling flux, rolling velocity, and rolling concentration was determined at 10 shear rates on P- and L-selectin, but only the rolling flux at a representative shear rate of 210 s−1 is shown. In control experiments, chimera-coated slides were incubated with mAb. (A) Rolling flux on P-selectin. Control experiment used the anti-P selectin (CD62P) mAb, G1. (B) Rolling flux on L-selectin. Control experiment used the anti-L selectin (CD62L) mAb, DREG-56. Data presented are from single experiments.

Rolling flux of CD34+ and CD34 FL cells on P- and L-selectin at a shear rate of 210 s−1.

Cells were subjected to wall shear rates from 487 s−1to 77 s−1 on P- or L-selectin chimeras adsorbed at 2 μg/mL on silanated glass. Rolling flux, rolling velocity, and rolling concentration was determined at 10 shear rates on P- and L-selectin, but only the rolling flux at a representative shear rate of 210 s−1 is shown. In control experiments, chimera-coated slides were incubated with mAb. (A) Rolling flux on P-selectin. Control experiment used the anti-P selectin (CD62P) mAb, G1. (B) Rolling flux on L-selectin. Control experiment used the anti-L selectin (CD62L) mAb, DREG-56. Data presented are from single experiments.

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