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OhmX Sample Preparation Guide

The OhmX Sample Prep Kit simplifies genomic research with a streamlined, amplification-free workflow that delivers results in just six hours. By tagging high-molecular-weight (HMW) DNA with proprietary labels at sequence-specific sites, this kit enables precise detection of structural variants (SVs) using Nabsys’ electronic genome mapping (EGM) technology. Designed for ultimate flexibility, it eliminates the need for library prep or barcoding and can be used with fresh or frozen samples, making it accessible even for researchers with no prior cytogenomics experience.

Perfect for detecting a wide range of genomic variations, the kit includes all necessary reagents for ten sample preparations, with each yielding enough material for multiple runs. Whether you’re working with cultured cells, blood, or bone marrow, the OhmX Sample Prep Kit offers a user-friendly and efficient solution to accelerate your research. Learn more at nabsys.com/learn/sample-prep-kit.

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Research Areas & Applications

Cancer Research
Genomic structural variations (SVs) encompass a diverse array of alterations involving large segments of the genome, such as deletions, duplications, inversions, translocations, and insertions.
Rare Disease
Structural variants are essential for diagnosing many genetic disorders and understanding their inheritance patterns.
Cell and Gene Therapy
In many patients, accurate detection and characterization of SVs are crucial for understanding disease etiology, developing targeted therapies, and designing effective gene delivery vectors.
Functional Genomics Research
DNA structural variations can impact gene expression and function. Identifying SVs is essential for deciphering the functional consequences of genetic variation.

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