Method for detecting phosphorylation level of intracellular tyrosine
A technology of phosphorylation level and detection method, which is applied in measurement device, fluorescence/phosphorescence, preparation of test samples, etc., to achieve the effect of speeding up progress, simple operation steps, and saving time and cost
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Embodiment 1
[0031] Flow cytometry was used to detect the level of intracellular tyrosine phosphorylation under exposure to low concentrations of smoke condensate in different smoking modes.
[0032] Smoke condensate preparation: extract cigarette samples according to GB / T 5606.1-2004, and use RM20H rotary table smoking machine to smoke under two smoking conditions of ISO and HCI respectively, the total particulate matter (Total Particulate Matter, TPM) use mm Cambridge filter discs were collected, and a corresponding volume of DMSO was added according to the quality of TPM to obtain a TPM stock solution with a final concentration of 10 mg / mL;
[0033] Cell infection: the cell density is 2.5×10 5 cells / mL were plated and cultured overnight. Add 120 μg / mL (respectively prepared under ISO and HCI suction conditions) of the cell culture medium of the smoke condensate for cell culture for 1 hour;
[0034] Immunofluorescence labeling and sample processing: the infected cells were washed th...
Embodiment 2
[0037] Flow cytometry was used to detect the level of intracellular tyrosine phosphorylation under exposure to high concentrations of smoke condensate in different smoking modes.
[0038] Smoke condensate preparation: extract cigarette samples according to GB / T 5606.1-2004, and use RM20H rotary table smoking machine to smoke under two smoking conditions of ISO and HCI respectively, the total particulate matter (Total Particulate Matter, TPM) use mm Cambridge filter discs were collected, and a corresponding volume of DMSO was added according to the quality of TPM to obtain a TPM stock solution with a final concentration of 10 mg / mL;
[0039] Cell infection: the cell density is 2.5×10 5 cells / mL were plated and cultured overnight. Add 300 μg / mL (respectively prepared under ISO and HCI suction conditions) of the cell culture medium of the smoke condensate for cell culture for 1 hour;
[0040] Immunofluorescence labeling and sample processing: the infected cells were washed thr...
Embodiment 3
[0045] The levels of intracellular tyrosine phosphorylation in cells exposed to low concentrations of smoke condensate in different smoking modes were detected by confocal laser microscopy.
[0046] Smoke condensate preparation: extract cigarette samples according to GB / T 5606.1-2004, and use RM20H rotary table smoking machine to smoke under ISO and HCI conditions respectively, TPM uses According to the mass of TPM, a corresponding volume of DMSO was added to obtain a TPM stock solution with a final concentration of 10 mg / mL.
[0047] Cell culture and treatment: Human oral epidermoid carcinoma KB cells were cultured in a-MEM complete medium containing 10% fetal bovine serum at 37°C, 5% CO 2 cultivated under conditions. When the cell confluency is 70%-80%, digest with trypsin, resuspend the medium to make a single cell suspension, and adjust the cell concentration to 4×10 4 cells / mL, inoculate 100 μL per well into a 96-well plate, and culture overnight. Add 40μg / mL flue gas...
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