Custom CRISPR Multiplex sgRNA Vectors
abm’s Custom CRISPR Multiplex sgRNA system allows for optimal expression of multiple sgRNAs from alternating U6 and H1 RNA pol III promoters on a single lentiviral vector. This allows for expression of multiple sgRNAs targeting a single gene or multiple sgRNAs targeting multiple different genes. sgRNAs may be designed for use with any Cas9 variant, which is expressed from a separate vector. Together, the Multiplex sgRNA Vectors expand the CRISPR toolkit allowing for highly diverse gene editing applications. Inquire with us below to get started on your custom CRISPR project.
Applications:
- Gene Activation using dCas9-VPR
- Gene Repression using dCas9-KRAB
- Epigenetic Gene Activation using dCas9-TET1CD
- Epigenetic Gene Repression using dCas9-DNMT3A
- Gene Knockout using spCas9
Service Details
Cloning Services
Lentivirus Packaging Services
Additional Info
Additional Resources
Documents
FAQs
| What promoter(s) are used in the Multiplex sgRNA vectors? |
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sgRNAs are expressed from alternating U6 and H1 promoters.
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| What is the approximate time frame to generate CRISPR lentiviral constructs? |
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The typical lead time is around 2-3 weeks for CRISPR lentivectors and 2-3 weeks for lentiviruses. Please inquire for a more accurate lead time.
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Citations
| 01 | Metzger D. et al. "Host Cell Transcriptional Tuning with CRISPR/dCas9 to Mitigate the Effects of Toxin Exposure." ACS Synth. Biol. (2022) 11, 3657-3668. doi: 10.1021/acssynbio.2c00214 |
| 02 | Shirasaki, T. et al. "Nonlytic Quasi-Enveloped Hepatovirus Release Is Facilitated by pX Protein Interaction with the E3 Ubiquitin Ligase ITCH." J. Virol. (2022) 96(21). doi: 10.1128/jvi.01195-22 |
