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Department of Growth and Differentiation
of Cell Populations


Head
Lucie Bacakova, M.D., Ph.D.

Deputy head
Vera Lisa, M.Sc.

Department staff:

Scientists
Assoc. Prof. Vladislav Mares, M.D., D.Sc.
 
Technical Assistant
Ivana Zajanova
 
Ph.D. Students
Elena Filova, M.Sc.
Jaroslav Chlupac, M.D.
Lubica Grausova, M.Sc.
Martin Parizek, M.Sc.
 
B.A. and M.A. Students
Barbora Vagaska, Faculty of Sciences, Charles Univ., Prague
Milan Smidl, Pedagogical Faculty, Purkinje Univ, Usti n. Labem
Ivana Koutna, Pedagogical Faculty, Purkinje Univ, Usti n. Labem
 
Joint Laboratory of Cancer
Cell Biology
 
Scientists
Prof. Aleksi Sedo, M.D., D.Sc.
 
Technical Assistant
Kveta Vlasicova
 
Ph.D. Students
Petr Busek, M.D.
Jarmila Stremenova, M.Sc.
 
M.A. Students
Petra Nytrova, lst Medical Faculty, Charles University, Prague
Iva Vomelova, Faculty of Sciences, Charles Univ., Prague
Jana Nemeckova, Faculty of Sciences, Charles Univ., Prague
 
 
 
 

 

Fig. 3. Human osteoblast-like MG 63 cells on day 14 after seeding on porous (A) or fibrous (B) scaffolds, made of a degradable copolymer of lactide and glycolide and designed for bone tissue engineering.
A:
Summarizing picture of horizontal optical sections. The depth of cell ingrowth onside the scaffolds with pore size of 400-600 mm is indicated with spectral colors (blue signal: 0 – 60 mm, green: 80 – 160 mm, yellow: 180 – 220 mm, orange: 240 – 300 mm, red: 320 – 400 mm, violet: 420 – 480 mm).
B:
MG 63 cells cultured in a dynamic perfusion cell culture system. The cell membrane is visualized with Texas Red C2-maleimide (red fluorescence), the cell nuclei with Hoechst #33342 (blue fluorescence). Confocal microscope Leica TCS SP2 AOBS, obj. 5x (A) or 10x (B).
C:
Dynamic perfusion cell culture system (Provitro GmbH, Berlin
D: Detail of the perfusion chamber for the cell-material complex.

 


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