Cell oxygen-deficient environment system constructed based on micro-numerical control living cell culture chamber
An environmental system and living cell technology, which can be used in tissue cell/virus culture devices, enzymology/microbiology devices, bioreactors/fermenters for specific purposes, etc. Problems such as large consumption of compressed air, to achieve the effect of simple operation and use, ease of movement and portability, and reduced operating costs
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Embodiment 1
[0016] Embodiment 1 Cell hypoxic environment system of the present invention
[0017] The cell hypoxic environment system mainly includes a hypoxic culture box, CO 2 Compressed gas, O 2 with N 2 Mixed compressed gas, gas circuit, numerical control device; among them, CO 2 Compressed gas, O 2 with N 2 The mixed compressed gas is respectively connected with the anoxic culture box through the air circuit, and the numerical control device is connected with the hypoxia culture box through the sensor.
Embodiment 2
[0019] The lid 1 and the box body 2 of the miniature numerically controlled anoxic culture box provided by the present invention are closed, and the temperature of the box lid and the box body and the humidity in the box are respectively controlled by the numerical control device, so that the inside of the culture box is always kept at 37°C and a humidity of 95%. .
[0020] When the anoxic culture system is working, first turn on the numerical control switch to make the box reach 37°C first, and then turn on the CO respectively. 2 Compressed gas, N 2 with O 2 Compressed gas, adjust the gas ratio through the numerical control device, so that the inside of the box reaches the required O 2 concentration, resulting in a hypoxic environment such as figure 1 shown.
Embodiment 3
[0022] Glial cells were cultured in a hypoxic culture box for a fixed period of time to characterize the feasibility and practicality of the hypoxia box
[0023] Glial cells were inoculated into a small dish, and the small dish was placed in a hypoxic culture box to continue culturing. After 24h, 48h, and 72h, photos were taken to observe the growth and proliferation of the cells, as shown in figure 2 shown.
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