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CRISPR/Cas genome editing enables targeted DNA cutting and gene insertion, removal, or modification, including single-nucleotide edits, for genetic-function analysis, model creation, and trait alteration. Select systems by target gene and cell type, Cas nuclease efficiency and specificity, guide RNA quality, and compatibility with experimental requirements.
View product category →Viral vectors are engineered virus particles that deliver DNA or RNA into living cells through transduction for molecular biology, cell culture, gene therapy, and vaccine development. Selection depends on cell-type specificity, transfer efficiency, safety, cargo capacity, vector stability, and whether temporary expression or stable genome integration is required.
View product category →All 2 product categories
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