The separation and identification of biomacromolecules such as nucleic acids and proteins constitute core experimental techniques in molecular biology. Traditional electrophoresis workflows are fragmented, with independent power supplies, electrophoresis tanks and imaging devices lacking systematic integration. Unstable voltage output, inconsistent buffer preparation and imprecise sample loading often cause band distortion, tailing and poor separation resolution, compromising molecular weight identification and semi-quantitative results. Tailored for nucleic acid and protein samples, our Electrophoresis Analysis Solution integrates electrophoresis hardware, supporting consumables and data analysis tools, establishing a complete workflow covering sample loading, biomacromolecule separation and band interpretation.

Sample pre-treatment serves as the initial step of all biological experiments, and sample quality directly determines the reliability of subsequent imaging, electrophoresis, and molecular detection results. Traditional manual sample processing is plagued by inconsistent mixing, poor homogenization performance, low operational repeatability, and high risks of human contamination. These issues frequently lead to experimental deviations and significant batch-to-batch variations. In most cases, experimental failures stem not from the detection stage, but from non-standardized preliminary sample preparation. Focusing on the entire workflow of biological sample pre-processing, our Sample Pre-treatment Solution integrates a full range of equipment for sample homogenization, vortex mixing, centrifugation and aliquoting, establishing a standardized sample preparation system. It delivers high-quality initial samples for downstream experiments including nucleic acid extraction, protein purification, molecular imaging and electrophoretic analysis.

Qualitative and quantitative analysis of proteins and nucleic acids constitutes the fundamental workflow of molecular biology laboratories. Traditionally, gel imaging and chemiluminescence detection rely on separate devices with inconsistent operating logic, incompatible data formats, and divergent band quantification criteria. This not only increases laboratory procurement and maintenance costs, but also leads to signal loss and quantification deviation, compromising the data reproducibility of Western blot, nucleic acid gel electrophoresis and other molecular experiments. Our Imaging and Analysis Solution integrates core gel imaging and chemiluminescence imaging capabilities into one unified molecular imaging platform, providing one-stop image acquisition and data analysis for nucleic acid gels, protein gels, Western blot chemiluminescence and other molecular assays.

Real-time tracking of biological signals has long been a core challenge in life science research. Traditional ex vivo detection methods rely on dissection and sampling of experimental subjects, which only acquire static data at discrete time points. Unable to continuously monitor the dynamic changes of biomarkers within living organisms, these conventional approaches easily miss critical temporal information, showing prominent limitations especially inin vivo animal tracing and phenotypic observation of living plants. To address this industry pain point, we launch the dedicated In-Vivo Imaging Solution. Covering both animal and plant living research scenarios, it builds an integrated non-invasive imaging system, enabling researchers to perform visualized acquisition and long-term dynamic monitoring of biological signals under intact living conditions.