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Are Flow Cytometry Based Isolation Technologies the Right Technology For Your Single-Cell Applications?

Dispense single cells sorted according to both fluorescence AND morphology with CYTENA’s F.SIGHT system. It embarks CYTENA image-based dispensing technology with green fluorescence sorting for more stringent single-cell isolation and confidence in monoclonality.

F.SIGHT 2.0

Trusted by Scientists Around the World 

WHY INVEST IN THE CYTENA SOLUTION?

The CYTENA Advantages Over the Pala Hana Systems

Clonality

SAVE TIME IN DISPENSING

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IMAGED-BASED TECHNOLOGY

Receive day 0 proof of monoclonality with embedded image-based technology.

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USING GFP FLUORESCENCE

Flow cytometry provides probabilities of monoclonality, but this remains probabilistic assurance, not proof.

Cell sorting based on flow cytometry Infer single-cell detection from fluorescence signals rather than detect cells, doublets or debris with a camera. For CLD work aimed at either peer-reviewed publication or IND-enabling work, this can be insufficient. Image-based cell sorting is as straightforward as it sounds. It is a reliable way to confirm the dispensing of single cells and to prove monoclonality to reviewers and regulators.

AppNote F.SIGHTTM – Fluorescence intensity-based isolation of single cells with assured clonality for CLD workflows

Combining the best of both world: fluorescence- and image-based dispensing.

The F.SIGHT only dispenses the single-cells that meet criteria for fluorescence, size and roundness. No fluorescence, no problem! You can also sort cells non-fluorescent cells solely on their morphology. Cell debris, doublet and single-cells are discarded. Pictures of the dispensing nozzle before, during and after dispensing serve as proofs of monoclonality.

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THE POWER OF THE CYTENA SOLUTION.

One Cell. One Well.

The F.SIGHT dispensing efficiency of 97% (number of wells with one cell dispensed) combined with an outgrowth rate up to 80% means that you get the highest colony-per-well rate of the industry. That’s fewer wells to seed, lower real-estate requirements in your incubator, less plate handling, less plastics... more efficiency overall, with

compounding benefits. The chances of a doublet growing into a colony unnoticed is about one in two million (Scherzinger et al.,). That’s only one non-clonal colony in about 5000x 384-well plates ; or one non-clonal colony once every 10 years at 10x 384-well plates per week.

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