Expression vector pEGFP-N1-p53/MAR capable of improving transfection efficiency, construction method and transfection method
A technology of pegfp-n1-p53 and pegep-n1-p53, which is applied in the construction method and transfection field of the expression vector pEGFP-N1-p53/MAR, can solve the problem of slow progress in chicken transgenic research
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Embodiment 1
[0117] Cloning of embodiment 1 human tumor suppressor gene p53
[0118] Experimental Materials
[0119] Human peripheral blood: The peripheral blood of patients with early-stage lung cancer was drawn in the First Affiliated Hospital of Henan University of Science and Technology, and ACD anticoagulant was added to the fresh peripheral blood and stored in liquid nitrogen at low temperature.
[0120] 1. Design and synthesis of primers for human tumor suppressor gene p53 gene cloning
[0121] The upstream and downstream primers Primera and Primerb were designed with reference to the complete sequence of the human tumor suppressor gene p53 in GenBank (accession number: NW_926584.1), and the primers were synthesized by Shanghai Sangon Bioengineering Technology Service Co., Ltd.
[0122] Upstream primer Primera: 5'-CCCAAGCTTATGGAGGAGCCGCAGTC-3' (SEQ ID NO.2)
[0123] Downstream primer Primerb: 5'-CGCGGATCCCAGTCTGAATCAGGCCCT-3' (SEQ ID NO.3)
[0124] 2. Extraction of total RNA from...
Embodiment 2
[0131] Example 2 Construction of recombinant plasmid pMD18-T-p53
[0132] For a schematic diagram of the construction process of the recombinant plasmid pMD18-T-p53, see figure 2 .
[0133] 1. Preparation of Competent Cells
[0134] (1) Take out the Escherichia coli E.coliJM110 strain from the refrigerator at -70°C, inoculate it in 5mL LB liquid medium, and cultivate it gently overnight at 37°C;
[0135] (2) Take 1 mL of the above-mentioned bacterial cell culture solution cultured overnight in a 1.5 mL centrifuge tube, centrifuge at 1500 r / min at 4 °C for 5 min, and discard the supernatant (note that the supernatant should be discarded as much as possible);
[0136] (3) Repeat step (2) 3 to 4 times;
[0137] (4) Add 100 μL of Solution A pre-cooled in ice to each centrifuge tube, flick the centrifuge tube gently to suspend the precipitate, and violent shaking is prohibited;
[0138] (5) Centrifuge at 1500r / min at 4°C for 5min;
[0139] (6) Add 100 μL of Solution B pre-coo...
Embodiment 3
[0185] Cloning of embodiment 3 chicken MAR gene
[0186] 1. Design and synthesis of primers for cloning of chicken MAR gene
[0187] Referring to the full sequence of the GenBank chicken MAR sequence (accession number: M58748.1GI:211883), the upstream and downstream primers to be amplified were designed and synthesized by Jiangsu Jinweizhi Engineering Technology Service Co., Ltd.
[0188] Upstream primer sequence (Primerc): 5'-TTTAGCGGCCGCCACTGTAGCCCTTA-3' (SEQ ID NO.4)
[0189] Downstream primer sequence (Primerd): 5'-CATCTTCTAGAGCTGGAAATGGCAAAC-3' (SEQ ID NO.5)
[0190] 2. Extraction of MAR gene in chicken liver tissue
[0191] The MAR sequence in chicken liver tissue was extracted using the Shanghai Animal Genome DNA Extraction Kit. The specific steps are as follows:
[0192] (1) Take 50mg of chicken liver tissue and put it into a homogenizer, add 100μL of BufferDigestion, grind it vigorously and quickly, transfer the ground tissue fluid into a 1.5ml centrifuge tube, and...
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