Human liver cancer cell line and its application for observing the life cycle of hepatitis B virus in cells
A liver cancer cell line, hepatitis B virus technology, applied in microorganism-based methods, cells modified by the introduction of foreign genetic material, and microorganism assay/inspection, etc., can solve the lack of sensitive cell lines and virus visualization methods, unable to truly confirmation, etc.
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Embodiment 1
[0049] Construction of eukaryotic expression vector pcHBV1.3-TC-1
[0050] 1. Obtain 1.3 times the hepatitis B virus gene
[0051] 1) Design primers, as follows:
[0052] Primers are as follows:
[0053]
[0054] 2) Reaction system
[0055]
[0056] Mix well by flicking, and centrifuge briefly to collect the liquid droplets on the tube wall to the bottom of the tube.
[0057] 3) PCR amplification
[0058] Pre-denaturation at 95°C, 5min
[0059] Cycle (30 times) 30s→95℃, 30s→58℃, 4min30s→72℃,
[0060] End extension 72°C, 5min
[0061] 4) Electrophoresis recovery and purification
[0062] (1) Add 500 μL of equilibrium solution to the CA2 adsorption column, centrifuge at 12,000 g for 30 s, and discard the supernatant.
[0063] (2) Cut off the target band and put it into a clean centrifuge tube.
[0064] (3) Add 3 times the volume of sol solution PN, and bathe in 50°C water until the glue block dissolves.
[0065] (4) Transfer the solution into a CA2 adsorption colum...
Embodiment 2
[0300] Take the above-mentioned eukaryotic expression vector pcHBV1.3-TC-1 as an example, transfect it into human liver cancer cells 1. Cell culture: Take out the frozen TC2 cells from the liquid nitrogen tank, shake them in a water bath at 37°C for 1 minute to dissolve them , add to a 10mL centrifuge tube containing about 5mL of DMEM medium, centrifuge at 1000rpm / min for 5min, remove the supernatant, add to a 75mL culture bottle containing 10mL of medium, place at 37°C, 5% CO 2 in the incubator.
[0301] After 24 hours, the medium was changed once, and when the cells grew to about 90% confluent, they were passaged according to the ratio of 1:2. Wait until there are enough cells for subsequent experiments.
[0302] Observing the cells under a microscope (*100), it was found that the cells could adhere to the wall 8 hours after thawing, and the cells were observed after 24 hours, and the cells were densely grown, growing in clusters, with abundant cytoplasm, one or more nuclei...
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