Method for carrying out cell density and arrangement controllable culture based on insect wing base
A technology of insects and cells, which is applied in the field of controlled cell density and arrangement based on insect wing substrates. It can solve the problems of simultaneous controllable cell density and arrangement, complex synthesis process, and damage to cell viability, so as to avoid complex process and safety. Problems, Ease of Access, Cell Viability Preservation Effects
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Embodiment 1
[0027] Cell Density and Arrangement Controlled Culture Based on Morpho Butterfly Wing Substrate
[0028] 1. Acquisition and fixation of Morpho butterfly scales:
[0029] Cut out rectangular morpho butterfly scale wing slices, and fix the wing slices with the back side up on a glass piece of the same size with polystyrene solution.
[0030] 2. Prepare cell suspension:
[0031] Select the fibroblasts of NIH / 3T3 mice, and dilute the fibroblasts with medium to a concentration of 2×10 5 / mL of cell suspension, put the resulting cell suspension into a glass container of a certain size.
[0032] 3. Cell sedimentation:
[0033] Insert the Morpho butterfly lepidopteran obtained in step 1 into the cell suspension prepared in step 2 at an inclination angle of 15° from the horizontal direction, and let stand at 37° C. for several hours.
[0034] 4. Obtain cell arrangement with directional arrangement and density gradient distribution:
[0035] The morpho butterfly scale wings in step...
Embodiment 2
[0037] Culture of two kinds of cells with controllable cell density and arrangement on the same morpho butterfly scale wing
[0038] 1. Acquisition and fixation of Morpho butterfly scales:
[0039] Cut out rectangular morpho butterfly scale wing slices, and fix the wing slices with the back side up on a glass piece of the same size with polystyrene solution.
[0040] 2. Prepare cell suspension:
[0041] Fibroblasts from NIH / 3T3 mice and bone marrow stem cells from MFC mice were selected and diluted with culture medium to a concentration of 2×10 5 / mL of cell suspension, put the resulting cell suspension into glass containers of a certain size.
[0042] 3. Cell sedimentation:
[0043] Insert the Morpho butterfly lepidopteran obtained in step 1 into the mouse fibroblast suspension prepared in step 2 at an inclination angle of 15° from the horizontal direction, let it stand at 37°C for several hours, take it out, and rinse with phosphoric acid flushing solution After several ...
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