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Phase contrast microscopy images of <t>mouse</t> <t>embryonic</t> <t>stem</t> <t>cells</t> in a culture device using the new chip design and a gas permeable lid. Images were taken in the same position at regular time intervals from the start of medium perfusion (0 h). Images were taken using a 10× objective and the scale bar represents 500 μm.
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Phase contrast microscopy images of <t>mouse</t> <t>embryonic</t> <t>stem</t> <t>cells</t> in a culture device using the new chip design and a gas permeable lid. Images were taken in the same position at regular time intervals from the start of medium perfusion (0 h). Images were taken using a 10× objective and the scale bar represents 500 μm.
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Phase contrast microscopy images of <t>mouse</t> <t>embryonic</t> <t>stem</t> <t>cells</t> in a culture device using the new chip design and a gas permeable lid. Images were taken in the same position at regular time intervals from the start of medium perfusion (0 h). Images were taken using a 10× objective and the scale bar represents 500 μm.
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Phase contrast microscopy images of <t>mouse</t> <t>embryonic</t> <t>stem</t> <t>cells</t> in a culture device using the new chip design and a gas permeable lid. Images were taken in the same position at regular time intervals from the start of medium perfusion (0 h). Images were taken using a 10× objective and the scale bar represents 500 μm.
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Phase contrast microscopy images of <t>mouse</t> <t>embryonic</t> <t>stem</t> <t>cells</t> in a culture device using the new chip design and a gas permeable lid. Images were taken in the same position at regular time intervals from the start of medium perfusion (0 h). Images were taken using a 10× objective and the scale bar represents 500 μm.
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Phase contrast microscopy images of <t>mouse</t> <t>embryonic</t> <t>stem</t> <t>cells</t> in a culture device using the new chip design and a gas permeable lid. Images were taken in the same position at regular time intervals from the start of medium perfusion (0 h). Images were taken using a 10× objective and the scale bar represents 500 μm.
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Phase contrast microscopy images of <t>mouse</t> <t>embryonic</t> <t>stem</t> <t>cells</t> in a culture device using the new chip design and a gas permeable lid. Images were taken in the same position at regular time intervals from the start of medium perfusion (0 h). Images were taken using a 10× objective and the scale bar represents 500 μm.
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Phase contrast microscopy images of <t>mouse</t> <t>embryonic</t> <t>stem</t> <t>cells</t> in a culture device using the new chip design and a gas permeable lid. Images were taken in the same position at regular time intervals from the start of medium perfusion (0 h). Images were taken using a 10× objective and the scale bar represents 500 μm.
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Image Search Results


Phase contrast microscopy images of mouse embryonic stem cells in a culture device using the new chip design and a gas permeable lid. Images were taken in the same position at regular time intervals from the start of medium perfusion (0 h). Images were taken using a 10× objective and the scale bar represents 500 μm.

Journal: Biotechnology Journal

Article Title: Robust, microfabricated culture devices with improved control over the soluble microenvironment for the culture of embryonic stem cells

doi: 10.1002/biot.201300245

Figure Lengend Snippet: Phase contrast microscopy images of mouse embryonic stem cells in a culture device using the new chip design and a gas permeable lid. Images were taken in the same position at regular time intervals from the start of medium perfusion (0 h). Images were taken using a 10× objective and the scale bar represents 500 μm.

Article Snippet: At an oxygen consumption of 5.6 × 10 –8 mol m –2 s –1 , reflecting a relatively high density of mouse embryonic stem cells, COMSOL® modeling shows that the gas permeable lid increases the uniformity of pericellular DO ( and ).

Techniques: Microscopy