Multiplexed experiments and enhanced workflows deliver unprecedented throughput
Guided wizard eliminates human error and improves reproducibility
Enhanced workflows dramatically increase productivity
C-Trap Accelerator Suite systematically targets every research bottleneck across your entire workflow: from sample preparation and instrument setup through workflow automation, experimental multiplexing, data analysis, training, and quality control. This complete ecosystem transforms both data quantity and quality, revolutionizing single-molecule research productivity.
Two independent microfluidics modules maximize data acquisition time by enabling flowcell cleaning in parallel with experimental execution, unlocking true back-to-back experiments. Parallel cleaning and measurement dramatically increases C-Trap throughput without compromising reproducibility.
A breakthrough DNA assembly kit multiplies experimental throughput by incorporating up to 50 identical binding sites into a single DNA construct. Collect up to 50x more binding events per experiment, shortening weeks of measurements into a single day data collection.
Golden Gate technology allows you to seamlessly ligate multiple DNA fragments in any desired order into a single backbone and test multiple target DNA sequences within one single C-Trap experiment. This enables assays like DNA sequence-specific looping and significantly accelerates sequence screening workflows.
Fast-track C-Trap user training and proficiency, support assay troubleshooting, and verify instrument performance with the C-Trap Reference Kit. The kit provides standardized and validated reagents for a complete DNA-protein binding assay, including data analysis with reference values.
Our new streamlined cleaning and passivation protocol with optimized reagents secures pristine channels and consistent single-molecule data. The 60-minute protocol removes all adsorbed proteins and chemicals and re-passivates the flow cell, extending its lifetime and improving reproducibility.
The on-screen guided setup guarantees optimal setup, boosting confidence for new and returning users. The visual wizard walks users step-by-step through the setup process, all the way up to the start of the experimental session, cutting setup time in half with zero guesswork.
Don't have a service contract?
Automated analytics convert raw C-Trap data into clear, publication-ready insights within minutes. The pre-built analysis pipelines extract key events and enable export figure-ready data and movies in one click.
Don't have Lakeview yet?
Here's how the full C-Trap accelerated workflow pays off. Using DNA repeat assembly kit, Bluelake, and Lakeview data analysis, LUMICKS researchers captured thousands of high-quality kinetic datapoints in a single afternoon session.
Our new interactive learning hub equips every user with step-by-step C-Trap expertise on demand. Bite-size modules and interactive materials turn novices into confident and proficient C-Trap single-molecule operators.
Structural Maintenance of Chromosome (SMC) complexes, cohesin, condensin and Smc5/6, play a fundamental role in genome organization, facilitating chromosome compaction, segregation, and DNA repair. Despite their essential functions, the mechanisms by which the complexes interact with different DNA substrates and influence topological transitions remain not fully understood. Using the LUMICKS C-Trap, we have employed single-molecule approaches to analyze the behavior of purified SMC complexes, focusing on yeast cohesin and human SMC5/6, on different DNA substrates, including double-stranded (dsDNA) and single-stranded DNA (ssDNA). Additionally, we have used a quadrupole optical trap to bridging by SMC complexes and their effect on DNA decatenation by Topoisomerase IIα (Top2A). These findings provide new insights into the fundamental properties and requirements of cohesin and Smc5/6’s interaction with DNA substrates, as well as their ability to bridge two independent DNAs.
Precisely manipulating genetic material at the single molecule level is gaining importance across life sciences – and so do the tools that allow researchers to do exactly that. The C-Trap system combines single molecule fluorescence microscopy with optical tweezers to manipulate DNA, allowing researchers to directly observe and track molecular events as they occur. Designing and creating specific DNA constructs is crucial for maximizing the potential of single molecule studies. In this application note we introduce the powerful combination of cutting edge biochemistry and single-molecule visualization methods to increase throughput and maximize the results gained from each individual measurement.