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HEMOSTASIS AND THROMBOSIS

Hydroxyl radical-modified fibrinogen as a marker of thrombosis: the role of iron

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Pages 241-247 | Published online: 18 Jul 2013

Figures & data

Figure 1. Effect of trivalent iron (ferric chloride) and divalent iron (ferrous sulfate) on the generation of hydroxyl radicals measured as fluorescence intensity of hydroxy-derivative of coumarin.

Figure 1. Effect of trivalent iron (ferric chloride) and divalent iron (ferrous sulfate) on the generation of hydroxyl radicals measured as fluorescence intensity of hydroxy-derivative of coumarin.

Figure 2. Conversion of soluble fibrinogen into insoluble aggregate, induced with iron and monitored as optical density OD values.

Figure 2. Conversion of soluble fibrinogen into insoluble aggregate, induced with iron and monitored as optical density OD values.

Figure 3. SDS-polyacrylamide gel electrophoresis of native fibrinogen unreduced – line 1; reduced – line 2; and of iron-modified fibrinogen unreduced – line 3; reduced – line 4).

Figure 3. SDS-polyacrylamide gel electrophoresis of native fibrinogen unreduced – line 1; reduced – line 2; and of iron-modified fibrinogen unreduced – line 3; reduced – line 4).

Figure 4. Scanning electron microscopy micrograph of a plasma sample obtained from a representative stroke patient. White stars indicate dense amorphous deposits intermingled with fibrin-like strands.

Figure 4. Scanning electron microscopy micrograph of a plasma sample obtained from a representative stroke patient. White stars indicate dense amorphous deposits intermingled with fibrin-like strands.

Figure 5. Scanning electron microscopy micrograph of a plasma sample with 10 μM ferric chloride. White stars indicate dense amorphous deposits intermingled with fibrin-like strands.

Figure 5. Scanning electron microscopy micrograph of a plasma sample with 10 μM ferric chloride. White stars indicate dense amorphous deposits intermingled with fibrin-like strands.

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