Cell chemotaxis analysis chip and device as well as use method and preparation method of cell chemotaxis analysis chip
A technology for analyzing chips and cells, which is applied in the field of biology, can solve the problems of difficult control of fluid flow, difficult experimental operation, etc., and achieve the effect of convenient and fast cell chemotaxis analysis test, convenient research, and simple steps
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Embodiment 1
[0062] Step 1, in figure 1 Use a puncher to punch through the middle circular liquid inlet chamber to obtain a millimeter-scale liquid inlet 1a for liquid inlet;
[0063] Step 2, fixing the cell chemotaxis analysis chip on the cell culture device, so that the cell chemotaxis analysis chip is in a vacuum state;
[0064] In this field, PDMS preplastics (siloxanes with two different chemical functional groups, A:B=10:1) are commonly used to make cell chemotaxis analysis chips. The main reason is that they have good light transmittance and Gas permeability and light transmission make it easy for experimenters to observe its internal conditions with a microscope, and gas permeability makes it easy to form a vacuum state to facilitate subsequent negative pressure operations. For example, the cell chemotaxis analysis chip can be put into a vacuum pump as a whole to use its own The air permeability of the cell chemotaxis analysis chip is evacuated; it is preferably 5-100Pa. Moreover...
Embodiment 2
[0072] Example 2: Analysis of the response of the same kind of cells to different chemokine solutions.
[0073] Step 1, human breast cancer cell line MDA-MB-231 cells were cultured with DMEM medium containing 10% serum (fetal bovine serum, FBS) and 1% penicillin-streptomycin (culture medium containing various amino acids and glucose, Gibco ), the 10% and 1% mentioned here are volume fractions, the same below, at 37°C and 5%CO 2 cultured in an incubator. The dissociated cells were treated with 0.25% Trypsin-EDTA (trypsin cell digestion solution) solution for 3-4 minutes, then neutralized by adding DMEM culture medium containing 10% FBS, centrifuged at 3000rpm, and discarded the supernatant. Wash the cells with 2% serum culture solution, centrifuge and resuspend to obtain a suspension containing cells.
[0074] Step 2, take two cell chemotaxis analysis chips, use a vacuum pressure pump (the model can be Millipore-WP6122050, the manufacturer Beijing Mintaiyuan Technology Co., L...
Embodiment 3
[0078] Example 3: Analysis of the response of different cells to the same chemokine solution.
[0079] Step 1, human breast cancer cell line MDA-MB-231 cells and human breast cancer cell line MCF-7 cells were respectively treated with DMEM culture medium containing 10% serum (fetal bovine serum, FBS) and 1% penicillin-streptomycin ( containing various amino acids and glucose, Gibco), at 37 °C and 5% CO 2 cultured in an incubator. The dissociated cells were treated with 0.25% Trypsin-EDTA (trypsin cell digestion solution) solution for 3-4 minutes, then neutralized by adding DMEM culture medium containing 10% FBS, centrifuged at 3000rpm, and discarded the supernatant. The cells were washed with 2% serum culture solution, centrifuged and resuspended to obtain two suspensions containing cells.
[0080] Step 2, take two cell chemotaxis analysis chips, and after evacuating with a vacuum pressure pump for 10 minutes, add the two cell suspensions into the two cell chemotaxis analysi...
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