Dharmacon
1) CRISPR-Cas9 Gene Editing
The Dharmacon Edit-R CRISPR-Cas9 platform greatly simplifies the workflow of permanently knocking out genes. The approach includes guaranteed, predesigned, ready-to-use guide RNAs and enables fast assessment of multiple target sites per gene for multiple genes.
You can choose from these products:
2) CRISPRa for Transcriptional Activation
Reagents provide a efficient set of tools to study a gene’s function by overexpression in its native context. Predesigned reagents for human and mouse genes make it easy! Using a deactivated or dead Cas9 nuclease fused to transcription activators, like dCas9-VPR, in combination with a guide RNA in either a synthetic or lentiviral format, the endogenous expression of a gene can be up-regulated.
Dharmacon offers these products:
3) RNA Interference
RNAi products contain the most complete portfolio of innovative tools for transient, long-term, inducible and in vivo RNAi applications. RNAi reagents are complemented with a complete suite of products for delivery, control and confirmation of results.
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4) cDNAs and ORFs
These products can be used to overexpress particular genes of interest. Choose from individual clones, lentiviral ORFs, and genome-scale libraries.
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5) Transfection
Transfection reagents for a wide range of applications. Lipid-based transfection reagents provides high efficiency delivery, low cellular toxicity and broad dynamic range.
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6) Viral Packaging
Package 2nd or 3rd generation viral vectors to consistently generate high-titer viral particles for gene silencing or gene expression studies.
Dharmacon offers Trans-Lentiviral shRNA Packaging Kits:
7) Services
Online design tools and extensive synthesis options to create custom products specific to your application.
Documents and resources
For more information visit producer's website.
CRISPRa for Transcriptional Activation
Lentiviral gene delivery allows the introduction and expression of a gene of interest in mammalian cells
Introduce the specific genetic material into eukaryotic cell by various methods of transfection
The unique and specific recombination system allows to edit genes in application as gene knockins or knockouts
The Cas9/sgRNA can be delivered into the target cells by AAV and lentiviral systems