Method for breeding rmnd5b (required for meiotic nuclear division 5homolog B) gene deletion type zebra fish through gene knockout
A gene deletion and gene knockout technology, applied in the field of gene knockout, can solve the problem of high off-target rate and achieve the effect of simple production, low cost and good medical research value
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[0084] The method for gene knockout breeding rmnd5b gene-deleted zebrafish is mainly completed through the following steps:
[0085] A. CRISPR / Cas9 gene knockout target site design
[0086] Query the genomic DNA sequence and functional domains of the zebrafish rmnd5b gene on the National Center for Biotechnology Information (NCBI), according to the principle of CRISPR / Cas knockout, on the website TheZiFiT Targeter (http: / / zifit.partners.org / ZiFiT_Cas9) Design a pair of target sites on the rmnd5b gene. The selection of targets must follow this standard: 5'-GG-(N)18-NGG-3'. The GG dinucleotide at the 5' end is part of the T7 promoter, and this restriction is not required when designing the target site, but it must be ensured that the 3' end of the target site is NGG. The selection of the target must ensure that the insertion or deletion of bases at the target position can affect the entire structural domain of the rmnd5b gene, thereby changing the expression of the gene.
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