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Cas9 DualGuide KO Vectors

Signosis offers a comprehensive suite of Cas9 DualGuide KO Vectors, featuring a single-vector design with dual-promoter sgRNA expression for each knockout target, optimized for enhanced knockout efficiency and targeting pathway regulators, kinases, and receptors with increased reliability

Principle 

Signosis offers our Cas9 DualGuide KO Vectors: a complete, ready-to-use solution for precise gene disruption across a broad range of cellular systems—no cloning, no design, no CRISPR expertise required. Just transfect and go.

Featuring a dual-sgRNA design driven by independent U6 and H1 promoters, this all-in-one vector ensures robust co-expression of Cas9 and two guide RNAs. This dual-sgRNA design enhances editing performance, boosting knockout efficiency, ensuring bi-allelic gene disruption, and reducing escape variants compared to single-guide or multi-vector systems. Studies show dual-sgRNA systems routinely achieve ≥ 60% editing in diverse cell types.

Optimized for pathway-focused research, our vectors support investigations into cell signaling pathways—without any CRISPR background.

Key features include:

  • All‑in‑one Cas9 + dual‑sgRNA plasmid: Simplifies delivery and ensures high co-expression—ideal for hard-to-transfect cells.

  • Independent U6 + H1 promoter control: Minimizes promoter interference and balances sgRNA expression for robust knockout.

  • High editing efficiency: Dual-guide strategy promotes ≥ 60% knockout rates and efficient bi-allelic disruption.

  • Pathway discovery, simplified: Prebuilt vectors targeting key regulators, with easy customization—just transfect and go.

  • Plug and Play: Pair with our TF Reporter Cell Lines for easy functional readouts.

  • Customization Targeting: Need to target a specific gene or pathway? We’ll help design and build a vector tailored to your research.

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Benefits

All-in-One Design

Cas9 and two sgRNAs in a single vector

Reliable Dual Targeting

Disrupts multiple regions of the same gene

Dual Promoter Expression

U6 and H1 minimize interference for balanced sgRNA levels

Easy Transfection

One vector simplifies delivery and reduces variability

Higher Knockout Efficiency

Up to 20–30% improvement over pooled sgRNA vectors

Customizable

sgRNAs can be tailored to your gene of interest

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