Construction of neural tube defect cell model and cell bank thereof under induction of hTERT recombinant
A cell model, recombinant technology, applied in recombinant DNA technology, cells modified by introducing foreign genetic material, libraries, etc., can solve problems such as inability to carry out research, and achieve the effect of normal differentiation and maintenance of chromosomes
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[0015] 1. Extraction of hTERT: ① Digestion of pClneo-hTERT: hTERT is located between the EcoRI and SalI sites of the plasmid pClneo-hTERT, and the multiple cloning site (MCS) of the pLXSNneo vector contains EcoRI and XhoI restriction sites. Commercially purchased pCIneo-hTERT plasmid, dissolved in an appropriate amount of ultra-clean H 2 In O or TE buffer, add 2uL 10× digestion buffer and 18uL H 2 O, add restriction endonuclease EcoR I and Xho I 0.5ul each, incubate at 37°C for 1h, heat at 75°C for 15min, inactivate the enzyme, add 5uL electrophoresis sample buffer (also by adding 0.5mol / L EDTA) The reaction was terminated, and hTERT was amplified according to the conventional PCR method, and the amplified product was collected for electrophoresis. ②hTERT electrophoresis: Take electrophoresis grade agarose and use electrophoresis buffer to make 10% agarose gel, pour it into the sealed gel filling platform, insert the sample comb, and remove the sealing tape from the gel makin...
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