Heterogeneous inverted flow chip and preparation method thereof
A flow chip and heterogeneous technology, applied in the field of micro-system chips, can solve the problems of insufficient safety and stability of detection probes, affecting chip quality and life, and poor packaging, etc., to achieve mass production, low cost, Effect of material and processing cost reduction
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Embodiment 1
[0025] Preparation of the lower support:
[0026] The lower support is made of PMMA sheet. Do the quality inspection of the board before production. The board should be of uniform thickness, smooth surface, no scratches on the surface and with a protective film, and the thickness of the board is 30mm. Cut the slabs into blanks of the designed shape with a stone cutting machine.
[0027] Use a fixed fixture to fix the blank, and use a milling machine to cut and repair the excess part. The cutting amount is 2mm, the feed rate is 250mm / min, the speed is 1000 rpm, the drilling speed is 1440 rpm, and the sinking drilling speed is 1440 rpm. The processing temperature is 20°C.
[0028] The blank processed by the milling machine is laser etched, and the micro-guiding groove of the flow chip is processed according to the given trajectory. The laser intensity is 50W, the moving speed is 250mm / s, and the temperature of the laser beam irradiation point is controlled at 370°C.
[0029]...
Embodiment 2
[0041] The preparation of the upper and lower supports is the same as in Example 1.
[0042] Chip preparation: After cleaning the chip substrate, air-dry the chip with dust-free low-humidity air at a temperature of 50°C at a flow rate of 0.1m / s for 30-45 seconds. After the chip substrate is dried, carry out antibody detection probes according to the antibody labeling process mark. Apply the fixing glue on the chip base, and dry it in dust-free low-humidity air at a temperature of 50°C at a flow rate of 0.1m / s for 15-20 seconds. The fixing glue on the chip base is in a semi-dry state.
[0043] The preparation of the monolithic chip is the same as in Example 1.
[0044] This embodiment can be used for protein molecular detection. Taking lactate dehydrogenase as an example, this test uses GENMED SCIENTICS INC U.S.A’s reagent as an example. Take 100ul of Tris-lactic acid buffer solution labeled as reaction solution A and mix it with 20ul of the reaction sample, react at 25°C for...
Embodiment 3
[0046] The preparation of the upper and lower supports is the same as in Example 1.
[0047] Chip preparation: After the chip substrate is cleaned and dried, the chip is air-dried in dust-free low-humidity air at a temperature of 50°C at a flow rate of 0.1m / s for 30-45 seconds. After the chip substrate is dried, nucleic acid detection is carried out according to the antibody labeling process Probe labeling. Apply the fixing glue on the chip base, and dry it in dust-free low-humidity air at a temperature of 50°C at a flow rate of 0.1m / s for 15-20 seconds. The fixing glue on the chip base is in a semi-dry state.
[0048] The preparation of the monolithic chip is the same as in Example 1.
[0049] This embodiment can be used for protein detection. Taking early pregnancy detection as an example, collect about 100ul of morning urine and inject it from the sampling port at one end of the upper support, and inject 100ul of the reaction solution from the other sampling port at the s...
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