Method for inducing apoptosis of human acute T lymphocytic leukemia cells by using Shuanghuanglian
A technology of leukemia cells and lymphocytes, which is applied in the field of inducing apoptosis of human acute T lymphocytic leukemia cells, can solve problems such as the effect of Shuanghuanglian that has not been found in research, and achieve the effects of optimizing treatment plans, promoting apoptosis, and inhibiting proliferation
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[0021] Example one:
[0022] S1. Resuscitate human acute T lymphocyte leukemia cells Jurkat, suspended in 10% fetal bovine serum (Gibco company) RPMI-1640 medium (Hyclone company), and then placed in a saturated humidity incubator at 37°C , CO in the incubator 2 The volume fraction is 5%;
[0023] In the pre-experimental study, it was found that the IC50 of Shuanghuanglian intervention for Jurkat cells for 48 hours was 72.35μg / ml respectively. In this experiment, Shuanghuanglian of 0μg / ml, 100μg / ml, 200μg / ml, 400μg / ml will be selected as the intervention concentration;
[0024] S2. Collect human acute T lymphocyte leukemia cells in logarithmic growth phase and adjust the cell density to 1.5 × 10 5 Pieces / ml to obtain cell suspension;
[0025] S3. Add 90μl of the cell suspension to each well of a 96-well plate, and then add 10μl of Shuanghuanglian at different concentrations to each well; add 10μl of serum-free RPMI 1640 medium to the negative control group, and set a blank zero group ...
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[0032] Embodiment two:
[0033] S1. Resuscitate human acute T lymphocytic leukemia cells Nalm-6, suspended in 10% fetal bovine serum (Gibco company) RPMI-1640 medium (Hyclone company), and then placed in a saturated humidity incubator at a temperature of 37℃, CO in incubator 2 The volume fraction is 5%;
[0034] In pre-experimental studies, it was found that the IC50 of Shuanghuanglian interfering with Nalm-6 cells for 48 hours was 164.5μg / ml respectively. In this experiment, we plan to choose Shuanghuanglian of 0μg / ml, 100μg / ml, 200μg / ml, 400μg / ml as the intervention concentration;
[0035] S2. Collect human acute T lymphocyte leukemia cells in logarithmic growth phase and adjust the cell density to 1.5 × 10 5 Pieces / ml to obtain cell suspension;
[0036] S3. Add 90μl of the cell suspension to each well of a 96-well plate, and then add 10μl of Shuanghuanglian at different concentrations to each well; add 10μl of serum-free RPMI 1640 medium to the negative control group, and set a bla...
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