siRNA interfering with mroh7 gene expression and its application, interfering method and drug
A gene expression and drug technology, applied in the field of molecular biotechnology and genetic engineering, can solve the problem of unclear function of Mroh7, and achieve the effect of improving cell viability
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Embodiment 1
[0045] This embodiment proposes siRNA that interferes with Mroh7 gene expression, that is, at least one of siRNA1, siRNA2 and siRNA3; the base sequence of siRNA1 is shown in SEQ ID NO.1, and the base sequence of siRNA2 is shown in SEQ ID NO.2. The base sequence of siRNA3 is shown in SEQ ID NO.3.
[0046] Search the AA sequence according to the Mroh7 mRNA sequence of the rat and record the 19 nucleotides adjacent to the 3' end of each AA base fragment, and screen the siRNA sequences with a GC content between 30% and 55%. Then make further screening according to the basic design principles of siRNA, and at the same time search the homology of the screened siRNA sequence in the genome database of GenBank with BLAST, select the sequence with more than 3 base mismatches with the non-homologous gene, and The possibility of non-specific inhibition was excluded, and three Mroh7 siRNA sequences were finally determined on the basis of meeting the above conditions.
[0047] In this embo...
Embodiment 2
[0053] The present embodiment proposes a method for interfering with Mroh7 gene expression, the steps are as follows:
[0054] 1.1 Dilute the siRNA that interferes with the normal expression of the Mroh7 gene with a serum-free medium to prepare an siRNA solution with a concentration of 10 μg / μL.
[0055] 1.2 Dilute the liposomes with serum-free medium to prepare a liposome solution with a concentration of 20 μg / μL;
[0056] 1.3 Mix the siRNA solution and the liposome solution to prepare a liposome-siRNA complex solution, and let it stand at room temperature for 20 minutes;
[0057] 1.4 In a 6-well culture plate, culture BRL-3A cells with 2 mL / well of complete medium, and the concentration of cells in each culture well is 3×10 5 a / mL;
[0058] 1.5 at 37°C, 5% CO 2 Carry out cell culture under the condition of saturated humidity until the cultured cells cover 40%-60% of the bottom area of the plate;
[0059] 1.6 Discard the medium in the culture well, and wash the cells 1-...
Embodiment 3
[0064] The present embodiment proposes a method for interfering with Mroh7 gene expression, the steps are as follows:
[0065] 1.1 Dilute the siRNA that interferes with the normal expression of the Mroh7 gene with a serum-free medium to prepare an siRNA solution with a concentration of 100 μg / μL.
[0066] 1.2 Dilute the liposomes with serum-free medium to prepare a liposome solution with a concentration of 500 μg / μL;
[0067] 1.3 Mix the siRNA solution and the liposome solution for 10 minutes to prepare a liposome and siRNA complex solution;
[0068] 1.4 Cultivate BRL-3A cells in the culture wells of the 6-well cell culture plate with 2 mL / well of complete medium, and the concentration of cells in each culture well is 6×10 5 a / mL;
[0069] 1.5 at 37°C, 5% CO 2 Carry out cell culture under saturated humidity conditions until the cultured cells cover 40%-60% of the plate area;
[0070] 1.6 Discard the medium in the culture well, and wash the cells 1-2 times with serum-free c...
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