<transcript><audio_141>cross Linker ratio of 65 is 1 and then not only that you make the substrate more cyto compatible that is compatible to cells by modification of</transcript><transcript><audio_142>the pdms substrate using aptma aptms and polycin and then you have to integrate not only you have to make this substrate you have to integrate this with a microfic setup then smaller d diameter of marker</transcript><transcript><audio_143>fluorescent beads like 0.046 plus minus 0.06 Micron can be placed very close to each other so typically eight number of bits in one micron square area allowing enhance spatial resolution of the</transcript><transcript><audio_144>TFM so in this way you can uh basically probe the Dynamics of a cell over length R so as I told you that what are the</transcript> cross Linker ratio of 65 is 1 and then not only that you make the substrate more cyto compatible that is compatible to cells by modification of the pdms substrate using aptma aptms and polycin and then you have to integrate not only you have to make this substrate you have to integrate this with a microfic setup then smaller d diameter of marker fluorescent beads like 0.046 plus minus 0.06 Micron can be placed very close to each other so typically eight number of bits in one micron square area allowing enhance spatial resolution of the TFM so in this way you can uh basically probe the Dynamics of a cell over length R so as I told you that what are the
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