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... Torrent/Proton NGS platforms Compatibility with most qPCR instruments Product Details The QIAseq Library Quant System provides a simple, out-of-the-box solution to quantify NGS libraries, enabling consistent ...
... atrophy) are included into NeuroLINCs panel. Features and benefits FIRST INCLASS TEST for the measurement of brain enriched IncRNAs in peripheral blood. FIRST TEST OF BLOOD LNCRNA BIOMARKERS for diagnostic ...
Result display time: 1 h
Sample volume: 0.6 ml
... proprietary innovative in vitro diagnostic (IVD) test designed and developed by Firalis for diagnostic applications in cardiac patients. FIMICs is a targeted sequencing (TS)-Next Generation Sequencing ...
... Product Overview
Pan-Solid Tumor High-Throughput
Sequencing Gene
Detection
Kit designed to target 425 genes associated with solid tumors and biomarkers for immunotherapy drugs, providing a comprehensive ...
... Product overview
The Pathogenic Microorganisms DNA/RNA Extraction
Kit (Catalog No.: SD-HMM-0011, 20 rxns) is designed for simultaneous extraction of DNA and RNA from a variety of biological samples. Extracted nucleic acids are ...
Result display time: 480 min
Sample volume: 1 ml - 500 ml
... >Product Description
- Product Name: Human SMN1/DMD/FMR1 mutation detection kit
- Certification: FDA
- Package Specification: 50 Tests/Kit
- Specification (pack option shown
Sample volume: 0.2 ml - 0.4 ml
... Genomic DNA Whole Blood Kit is designed to allow automated processing of multiple sample types in the same run. Contents Pre-Filled Cartridge Reagent ( 48 pcs/Box x 2 Box) Pipette Tip and Holder Set ( 100 pcs/Box ...
... Uncover transcription factor (TF) occupancy Diagenode’s ATAC-seq kit is based on a highly validated protocol optimized for 50,000 cells per reaction. The kit includes the reagents for cell lysis and ...
Result display time: 4 h
Tumor is the neoplasm of normal tissue, of which cancer is malignant neoplasm driven by various of tumorigenesis factors. Gene mutations caused by environment and heredity (including point mutation, deletion, insertion, copy number gain, gene fusion and ...
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