A dry cell model and its establishment method and application
A cell model and method-building technology, applied in artificial cell constructs, animal cells, vertebrate cells, etc., can solve the problem of large influence on the stability of experimental results, unstable wind speed of ultra-clean typhoons, and poor uniformity of wind speed, etc. problems, to achieve the effect of high accuracy of result evaluation, easy operation and high reproducibility of results
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experiment example 1
[0139] Experimental example 1 Desiccator method prepares the dry cell model of human skin fibroblast
[0140] 1.1 Test material
[0141] Experimental materials: human skin fibroblasts, RPMI-1640 medium, fetal bovine serum (FBS), trypsin.
[0142] Main equipment: glass desiccator (diameter 300mm), temperature and hygrometer, inverted microscope, ultra-clean workbench, carbon dioxide incubator.
[0143] 1.2 Experimental method and process
[0144] 1.2.1 Preparation before experiment
[0145] Prepare a glass desiccator and add 500 g of silica gel to dry the particles (4 hours at 120° C. in an oven). Seal it for 1 hour, measure the relative humidity in the desiccator to be 10.0%, the temperature is 25° C., and irradiate for 1 hour under the ultraviolet lamp.
[0146] 1.2.2 Planking
[0147] Take 5×10 4 Cells / mL The recovered human skin fibroblasts of the third generation were inoculated on a 96-well plate, 125 μL per well, and 5 replicate wells were set for each sample. At ...
experiment example 2
[0159] Experimental Example 2 Desiccator Method Preparation of Dry Cell Model of Human Skin Fibroblasts
[0160] 2.1 The specific parameters are the same as in Experimental Example 1, where the drying time in 1.2.3 is replaced with 30 minutes.
[0161] 2.2 Results and analysis
[0162] The experiment was repeated three times, and the cell viability is shown in Table 2 below.
[0163] Table 2 Cell viability (%)
[0164]
[0165] Note: ** means p<0.01 compared with the non-dried treatment group
[0166] Conclusion: It is feasible to use a desiccator to dry and damage cells, and the error of three parallel experiments is within 5.0%. The drying damage effect of Experimental Example 2 is more significant.
experiment example 3
[0167] Experimental example 3 Desiccator method prepares human skin keratinocyte drying model
[0168] 3.1 Experimental materials
[0169] Experimental materials: human skin keratinocytes (HaCaT), DMEM high-glucose medium, fetal bovine serum, trypsin.
[0170] Main equipment: glass desiccator (300mm in diameter), inverted microscope, ultra-clean bench, carbon dioxide incubator, temperature and humidity meter
[0171] 3.2 Experimental method and process
[0172] 3.2.1 Preparation before experiment
[0173] Prepare a glass desiccator and add 500 g of silica gel to dry the particles (4 hours at 120° C. in an oven). Seal it for 1 hour, measure the relative humidity in the desiccator to be 9.0%, the temperature is 26°C, and irradiate for 1 hour under the ultraviolet lamp.
[0174] 3.2.2 Planking
[0175] Take 5×10 5 Seed the human skin keratinocytes of the third passage after resuscitation in a 96-well plate at a density of cells / mL, 100 μL per well, 37 ° C, 5% CO 2 Conditio...
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