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1) Detachment of cells by control of temperature.

2) Comparison of re-attachment kinetics for harvested A-549 cells between UpCell/RepCell (UpCell with Grid) and trypsin.

3) Comparison of harvested extra cellular matrix between UpCell/RepCell (UpCell with Grid) and dispase (E-cadherin).

4) Comparison of flow cytometry application between UpCell/RepCell (UpCell with Grid) and trypsin.

5) Comparison of detachment of macrophage between UpCell/RepCell (UpCell with Grid) and trypsin.

6) Comparison of re-attachment of macrophage between UpCell/RepCell (UpCell with Grid) and trypsin.

7) Protocol for macrophage collection in single cell suspension

8) Protocol for dendritic cell collection in single cell suspension.

9) Protocol of NIH/3T3 cell-sheet transfer using membranes for UpCell 3.5cm.

10) Application data for mono-layered cell-sheet.

11) Application data for multiple layered cell-sheet (3D tissue constructs).

Upcell/RepCell (UpCell with Grid) data

5) Comparison of detachment of macrophage between RepCell and trypsin.

Normal culture
@ 37 degrees celsius
30 min post-cool
@ 20 degrees celsius
Removal after
slight agitation
Peritoneal macrophage (mouse)

Recovery ratio of peritoneal macrophages (mouse)

1) Seed 5x106 of peritoneal macrophages (mouse) on 1 (one) RepCell and 2 (two) tissue culture treated 6cm dish respectively.
2) Incubate for 2 hours, and wash off anchorage-independent cells by PBS.
3) Further culture for 2 days. Replace medium with PBS. Detach cell by temperature (on ice, 5min) for RepCell, 2.5ml trypsin and EDTA/scraping for tissue culture dishes, followed by measurement.

Recovery ratio of macrophage (human)

1) Seed 5x106 of HL-60 onto RepCell and tissue treated cell culture dish (6cm). Add 100nm PMA (Phorbol 12 Myristate 130 Acetate) to induce cells to macrophages.
2) Culture for 5 days and replace medium with PBS. Detach cells by temperature (25°C, 30min) for RepCell and EDTA/PBS for tissue culture treated dish.
(Prof. Kobayashi, Toho Univ. Biosci.)