High quality RNA, DNA and protein is crucial for facilitating breakthroughs in molecular research and diagnostics. Traditional phenol/chloroform or Silica based extraction methods often struggle to provide high quality and purity DNA and RNA, especially from challenging sample types, such as tissues, stool, saliva, and other bodily fluids. Moreover, correct sample collection and preservation methods are as crucial as isolation. For lab managers and researchers, streamlining these processes with simplified workflows while maintaining accuracy is essential for saving time and ensuring reproducibility.
Adopting optimized preservatives and new proprietary Silicon Carbide technology for extraction of RNA, DNA, Protein and Exosomes can substantially enhance the purity and reliability of results, especially for studies involving critical applications such as cancer biomarker research. Integrating high-throughput and automation friendly extraction methods further optimizes efficiency, enabling researchers to handle larger sample volumes with consistent precision. Additionally, embracing single-step, multi-analyte extraction techniques allows labs to work effectively with limited sample quantities, simplifying workflows and minimizing variability, ultimately leading to greater operational efficiency and consistency in data quality.
Download this compilation of white papers to unlock actionable insights to:
- Reduce biases in RNA extraction and ensure more reliable results
- Enhance your diagnostic applications with accurate miRNA detection methods
- Improve lab efficiency with streamlined, single-sample extraction for RNA, DNA, and proteins
