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Cut |
Wild type Cas9 efficiently generates double strand breaks (DSBs) at sequences homologous to co-expressed gRNA. |
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Nick |
A mutated "nickase" version of the Cas9 enzyme generates a single-strand DNA break (Nick), instead of a double-strand DNA break (Cut). |
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Interfere |
A catalytically inactive Cas9 (dCas9) can knockdown gene expression by interfering with transcription. The dCas9 can sometimes be fused to an additional repressor peptide. |
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Activate |
A catalytically inactive Cas9 (dCas9) fused to an activator peptide can activate or increase gene expression. |
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dCas9-FokI |
A catalytically inactive Cas9 (dCas9) fused to FokI nuclease to generate double strand breaks (DSBs, Cut) at sequences homologous to two co-expressed gRNA. |
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Purify |
Isolate specific genomic regions of interest using a catalytically inactive Cas9 (dCas9) fused with an epitope tag(s). |
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Visualize |
Visualize specific genomic regions of interest using a catalytically inactive Cas9 (dCas9) fused to a fluorescent protein. |
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Screen |
Use pooled CRISPR libraries to screen for genes involved in specific biological processes. |
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Tag |
Find the tools for tagging your endogenous protein of interest. |
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Validated gRNAs |
Experimentally validated, pre-made gRNA plasmids to specific genes. |
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Empty gRNA Vectors |
Select a gRNA plasmid based on a variety of factors, such as presence or absence of Cas9 and number of gRNAs (multiplex vectors). |