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Questions related from Maryam Ansari
Dear All, I want to cut PDMS sheet with thickness of 0.8 mm to rectangular shape with Graphtec cutter plotter CE6000-40. What condition do you offer? Do you offer any kind of special speed or force?
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I want to use the TriFECTa RNAi kit for transfection, but I dont know how much RNA and control transfection should I use.
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Is it changed it 3D structure and damage the structure or not?
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At first, when I culture cells I could obviously see cells in channels that moving through the channels, but after 24 hour there is no cell.
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What is the most efficient time to oxygen plasma of PDMS to increase the hydrophilicity?
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