Application of autophagy-related protein 12 in the prevention and treatment of enterovirus 71 infection
A technology of autophagy-related protein and enterovirus, applied in the field of biomedicine
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[0049] 1. Design and synthesize specific siRNA sequences for each host cell molecule.
[0050] 1.1 For each target gene, search NCBI GeneBank to obtain the full sequence and mRNA sequence, use existing network resources and common software to carry out biological analysis of each target gene, and select the coding region as the target sequence for siRNA design. Refer to the principle of siRNA design and compare it with the human genome sequence through the blast function of the GeneBank database to ensure no homology; exclude potential siRNAs that pair with other genes with 8 consecutive bases at the 5' end of the aitisense chain; exclude any continuous 14 nucleotides potential siRNAs for base pairing with other genes. The design software was used for pre-assessment and determination, and 3 optimal kinetic parameter targets were selected to enter the subsequent experimental process. A total of 3 interference sequences were synthesized for each gene, as shown in Table 1.
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