Figure 4.
Binding kinetics of PF4-specific Abs from VITT samples in the presence of different anticoagulants. Biotinylated PF4 (5 µg/mL) was immobilized on streptavidin biosensor tips, and binding kinetics of serum samples from patients with VITT (n = 5) were analyzed using BLI. For dissociation, different anticoagulants (heparin, 0.1 U/mL [pink]; heparin, 1 U/mL [dark red]; danaparoid, 0.8 U/mL; fondaparinux 8 µg/mL; argatroban 8 µg/mL) or Octet buffer were applied. Curves and data points represent the mean of technical duplicates (n = 2). (A) Schematic illustration of the experimental setup. (B) Representative binding responses of PF4-specific Abs from a VITT patient serum (VITT1). (C) Quantification of residual binding in percent at time point 560 secondsof the dissociation (percent Residual Binding T560s) of VITT serum samples.

Binding kinetics of PF4-specific Abs from VITT samples in the presence of different anticoagulants. Biotinylated PF4 (5 µg/mL) was immobilized on streptavidin biosensor tips, and binding kinetics of serum samples from patients with VITT (n = 5) were analyzed using BLI. For dissociation, different anticoagulants (heparin, 0.1 U/mL [pink]; heparin, 1 U/mL [dark red]; danaparoid, 0.8 U/mL; fondaparinux 8 µg/mL; argatroban 8 µg/mL) or Octet buffer were applied. Curves and data points represent the mean of technical duplicates (n = 2). (A) Schematic illustration of the experimental setup. (B) Representative binding responses of PF4-specific Abs from a VITT patient serum (VITT1). (C) Quantification of residual binding in percent at time point 560 secondsof the dissociation (percent Residual Binding T560s) of VITT serum samples.

Close Modal

or Create an Account

Close Modal
Close Modal