Solution reagent kit NanOnCT
for researchclinicalliquid

Solution reagent kit - NanOnCT - Nanodigmbio Co., LTD - for research / clinical / liquid
Solution reagent kit - NanOnCT - Nanodigmbio Co., LTD - for research / clinical / liquid
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Characteristics

Type
solution
Applications
clinical, for research
Format
liquid
Tested parameter
BRCA1 gene, BRCA2 gene, for PMS2 gene, gene ROS1, RET gene, FGFR Fusion GENE, for BRAF gene, for PIK3CA Gene, for PTEN gene

Description

NanOnCT Panel v1.0 is a compactable panel designed for analysis of solid tumors and liquid biopsy. This panel involves a total number of 69 genes with selected regions covered. With an optimized probe design, this panel offers a highly uniform coverage over targeted regions for both FFPE and cell-free DNA. Can RNA samples be directly used for library preparation with this kit? No. This kit is compatible only with gDNA or cDNA as initial samples. For RNA samples, reverse transcription to generate cDNA is required prior to library preparation. What is the recommended input range? How to handle inputs exceeding this range? This kit supports 50-2,000 ng of gDNA or cDNA. For input amount exceeds 2,000 ng, split the sample into multiple reactions to maintain amplification efficiency. What is the insert size of this kit? How to select sequencing read length? The main peak of PCR products by using this kit is ~270 bp. PE150 sequencing is recommended for high-quality coverage. What is the recommended sequencing data volume for IGTR immune repertoire analysis? A minimum of 0.3 Gb is recommended to detect clones at 0.01% abundance with an input of 200 ng. Increase data volume to enhance sensitivity for low-frequency clones. Is this kit suitable for minimal residual disease (MRD) monitoring? Yes. This kit includes IG Primer Mix and TR Primer Mix with gene-specific primers provided in separate tubes, allowing flexible combination in a single amplification reaction. With its high sensitivity, the kit meets the requirements for MRD monitoring technology development and clinical applications, making it ideal for low-frequency variant detection scenarios.

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