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Fibrin in human plasma: Gel architectures governed by rate and nature of fibrinogen activation
Thrombosis Research, Vol. 76, No. 5, pp. 501-502.1994 Copyright Q 1994 Elsevier Science Ltd Printed in the USA. All rights reserved 0049-3848/94 $6.00 + .oO
Pergamon
0049-3W3(94)EOO164-2
ERRATUM THROMBOSIS RESEARCH 75,521~538,1994 “Fibrin in human plasma: Gel Architectures governed by rate and nature
of fibrinogen activation” B. BlombBck, K. Car&on, K. Fatah, B. Hessel and R. Procyk At the this
authors’ request, figures SA and 5B on page 531 are being reprinted for clarity on page and the following page.
a FIG. 5 A.
b
d
e
Confocal laser 3D microscope pictures of fibrin gel net works in recalcified plasma at different thrombin concentrations. Gel formation: To 1 ml of plasma was added 20 ul of CaC12 (1 M) and 50 ul of thrombin (human) of different concentrations. Flow chambers were filled (SO100 ~1) by capillary force and the plasma allowed to gel for 1% 24 hours at room temperature. Fibrinogen concentration, 2.7 mg/ml. Gel permeation: with Tris-imidazole-NaCl buffer containing radioactive alanine as described in legend to Fig. 4. Small letters (a-e) refer to corresponding experiments indicated in Table I A. Computer generated stereopairs are presented. For further information see Materials and Methods.
502
ERRATUM
Vol. 76, No. 5
FIG. 5 B.
b
c
d
Confocal laser 3D microscope pictures of fibrin gel net works in recalcified plasma at different thrombin concentrations. Gel formation: To 1 ml of plasma was added 20 u.l of CaCla (1 M) and 50 ul of thrombin (human) of different concentrations. Flow chambers were filled (50-100 n.l) by capillary force and the plasma allowed to gel for 18-24 hours at room temperature. Fibrinogen concentration, 2.7 mg/ml. Gel permeation: with Trisimidazole-NaCl buffer containing radioactive alanine as described in legend to Fig. 4. Small letters (a-d) refer to corresponding experiments indicated in Table I B. Computer generated stereopairs are presented. For further information see Materials and Methods.
Pergamon
0049-3W3(94)EOO164-2
ERRATUM THROMBOSIS RESEARCH 75,521~538,1994 “Fibrin in human plasma: Gel Architectures governed by rate and nature
of fibrinogen activation” B. BlombBck, K. Car&on, K. Fatah, B. Hessel and R. Procyk At the this
authors’ request, figures SA and 5B on page 531 are being reprinted for clarity on page and the following page.
a FIG. 5 A.
b
d
e
Confocal laser 3D microscope pictures of fibrin gel net works in recalcified plasma at different thrombin concentrations. Gel formation: To 1 ml of plasma was added 20 ul of CaC12 (1 M) and 50 ul of thrombin (human) of different concentrations. Flow chambers were filled (SO100 ~1) by capillary force and the plasma allowed to gel for 1% 24 hours at room temperature. Fibrinogen concentration, 2.7 mg/ml. Gel permeation: with Tris-imidazole-NaCl buffer containing radioactive alanine as described in legend to Fig. 4. Small letters (a-e) refer to corresponding experiments indicated in Table I A. Computer generated stereopairs are presented. For further information see Materials and Methods.
502
ERRATUM
Vol. 76, No. 5
FIG. 5 B.
b
c
d
Confocal laser 3D microscope pictures of fibrin gel net works in recalcified plasma at different thrombin concentrations. Gel formation: To 1 ml of plasma was added 20 u.l of CaCla (1 M) and 50 ul of thrombin (human) of different concentrations. Flow chambers were filled (50-100 n.l) by capillary force and the plasma allowed to gel for 18-24 hours at room temperature. Fibrinogen concentration, 2.7 mg/ml. Gel permeation: with Trisimidazole-NaCl buffer containing radioactive alanine as described in legend to Fig. 4. Small letters (a-d) refer to corresponding experiments indicated in Table I B. Computer generated stereopairs are presented. For further information see Materials and Methods.