Sunday, June 22, 2025

KROMATID Launches KROMASURE(TM) PinPoint: Next Generation, High-Throughput Transgene Integration Analysis

KROMATID, a leader in structural genomics innovation, is proud to announce the release of an expanded capability for its Advanced Cytogenetics Platform. KROMASURE PinPoint provides a proprietary high-throughput solution designed to redefine the standards of transgene genomic integration analysis. With single-cell resolution and unmatched sensitivity, PinPoint empowers researchers to detect integration events as small as 2kb-with the ability to screen up to 1,000 individual cells in a single experiment.

Optimized for Cell and Gene Therapy development, PinPoint delivers precise, quantitative insight into transgene insertional copy number and modal distribution on a single-cell basis, enabling the identification of low-prevalence events that are typically missed by pooled assays. This sets a new benchmark for supporting regulatory compliance and risk profiling in gene therapy and cell line development.

“PinPoint is not just a product-it’s a transformation in how we visualize and understand transgene insertion,” said Erin Cross, VP of Platform at KROMATID. “With its high-resolution, interphase-capable design, PinPoint meets the growing demand for rigorous, scalable, and compliant genomic analysis-even in non-dividing cells where traditional metaphase-based methods fall short.”

Also Read: Pangea Laboratory Appoints John Moore as Chief Executive Officer

A New Approach to Advance Transgene Integration Analysis

While sequencing and ddPCR have long been the standards for assessing insertional copy number, they are limited by their reliance on pooled cell populations—obscuring the cell-to-cell variability that is critical for accurate characterization. By analyzing individual cells, developers can now detect small targets, visualize rare integration patterns, and understand the true distribution of copy number across a population.

“We’re now able to visualize and profile transgene integrations in thousands of single cells,” said Cross. “This expanded capability gives developers a clearer picture of how their editing machinery performs at the cellular level, helping them understand transgene distribution with far greater precision than pooled average measurements can provide.”

SOURCE: PRNewswire

Subscribe Now

    Hot Topics