- Gene editing
- Gene editing reagents
- Edit-R synthetic sgRNA positive controls
Edit-R synthetic sgRNA positive controls
Synthetic sgRNA controls to verify optimal parameters for CRISPR-Cas9 gene editing
Positive control sgRNA for confirming gene editing with your experimental conditions, provided with or without primers for DNA mismatch detection assays.
Edit-R Synthetic sgRNA controls are recommended as positive controls for CRISPR-Cas9 experiments utilizing synthetic sgRNA to optimize transfection conditions and verify Cas9 nuclease expression.
Gene-specific positive controls and kits are designed and validated for mismatch detection assays to verify gene editing experiments. They are configured as follows:
- Individual Edit-R synthetic sgRNA control to edit human or mouse PPIB, or DNMT3B
- Edit-R synthetic sgRNA control kits contain the following:
- Edit-R synthetic sgRNA control (PPIB or DNMT3B)
- Mismatch detection assay forward primer (PPIB or DNMT3B) - 5 nmol
- Mismatch detection assay reverse primer (PPIB or DNMT3B) - 5 nmol
Edit-R lethal synthetic sgRNA controls are universal positive controls designed to induce cell death in a dose- and Cas9-dependent manner by targeting multiple repeat regions in the genome.
Edit-R lethal synthetic sgRNA control #1 induces very potent cell death, while lethal control #2 induces moderate cell death. These controls span a large dynamic range and allow for the optimization of CRISPR-Cas9 delivery for observation of both strong and moderate CRISPR-Cas9 phenotypes. Read the blog, "A lethal positive control for CRISPR knockout" to learn more about these controls.
- R. Barrangou, A. Birmingham,et. al.Advances in CRISPR-Cas9 genome engineering: lessons learned from RNA interference.Nucleic Acids Research,43(7) 3407-3419 (2015)
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M.L. Kelley, Ž. Strezoska, et al. Versatility of chemically synthesized guide RNAs for CRISPR-Cas9 genome editing. J. Biotechnol. 233, 74–83 (2016). doi:10.1016/j.jbiotec.2016.06.011
Application notes
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Edit-R Lethal crRNA controls for transfection optimization and ongoing monitoring of CRISPR-Cas9 experimental conditions - Application Note
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Homology-directed repair with Dharmacon Edit-R CRISPR-Cas9 reagents and single-strand DNA oligos - Application Note
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Optimization of reverse transfection of Edit-R synthetic crRNA and tracrRNA components with DharmaFECT transfection reagent in a Cas9-expressing cell line - Application Note
Posters
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2'-O-methyl phosphorothioate linkage-modified synthetic guide RNAs for efficient CRISPR-Cas9 genome editing and reduced cellular toxicity - Poster
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A Synthetic CRISPR-Cas9 System for Homology-Directed Repair - Poster
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An algorithm for selecting highly functional and specific guide RNAs for CRISPR-Cas9 gene knockout - Poster
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Complete alignment identification of CRISPR-Cas9 genomic off-targets using Edit-R CRISPR specificity tool - Poster
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CRISPR-Cas9 genome editing utilizing chemically synthesized RNA - Poster
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Homology-directed repair with Edit-R CRISPR-Cas9 and single-strand DNA oligos - Poster
Product data
Product inserts
Protocols
Quick protocols
Safety data sheets
Technical manuals
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CRISPR-Cas9 genome engineering with Cas9 nuclease expression plasmids and Edit-R synthetic RNA - Technical Manual
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CRISPR-Cas9 genome engineering with inducible lentiviral Cas9 nuclease and Edit-R guide RNAs - Technical Manual
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CRISPR-Cas9 genome engineering with lentiviral Cas9 particles and Edit-R synthetic guide RNA - Technical Manual
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