Biochemical method for detecting ionizing radiation dose
A technology of ionizing radiation and biology, applied in the field of biological detection of radiation dose, can solve the problems of high detection cost, complicated operation, and many subjective factors, and achieve the effect of improving accuracy
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[0016] 1) Irradiation conditions and experimental grouping: HMy2.CIR human B lymphoblastoid cells in the logarithmic growth phase (1×10 6 Cells / dish) were seeded in 60mm culture dishes, cultured for 24h, and the cells were irradiated with low doses of 1.6, 3.2, 4.8, 6.4, 8cGy or high doses of 0.4, 1, 2, 4, 8, 12, 16, 20Gy at room temperature Dose irradiation, and set up a blank group without irradiation at the same time, each group set up three repetitions (n=3).
[0017] 2) Immediately after the cells were irradiated, the cells were incubated in fresh culture medium containing 3 μg / ml cytochalasin B (Sigma Company) and continued to culture for 24 hours.
[0018] 3) Transfer the cells into a 15ml centrifuge tube, centrifuge at 300g for 10min to remove the culture medium, add 7ml 0.075M KCl to each tube, mix well, and hypotonic at room temperature for 10min.
[0019] 4) Add 1ml of fixative solution (by mass ratio, methanol: glacial acetic acid 9:1) to pre-fix the cells.
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