Cellecta’s LINE-1 Assay Kit provides a convenient, efficient, and targeted Next-Generation Sequencing (NGS) based approach to identify polymorphic insertion sites of LINE-1 in the human genome. The LINE-1 Assay Kit includes all the components needed to detect and identify novel LINE-1-induced genomic variations in genomic DNA isolated from tumors, blood, cells or other samples. Only a few hundred nanograms of DNA are requir…
Reliable detection of cancer-associated mutations in 597 genes from liquid biopsy samples
For low-to-medium throughput NGS needs, the Zephyrâ„¢ G3 NGS workstation is a compact, semi-automated solution designed to construct up to 96 NGS libraries per day. This compact workstation is equipped with a highly precise, 96-channel pipetting head and includes an integrated gripper. For Research Use Only. Not for use in diagnostic procedures.
The NEXTflex® Dual-Indexed DNA Barcodes are two kits that each contain 96 combinatorial dual indexed barcoded adapters for Illumina® library prep which enable deep multiplexing of NGS sequencing samples compatible with high-throughput automation.They significantly increase scale, while reducing costs by allowing the user to pool up to 192 samples in a single flow cell.
SMARTer smRNA-Seq Kit for Illumina—Sequence Small RNAs with High Sensitivity and Minimal Bias
SMARTer Human TCR a/b Profiling Kit—Obtain Full-Length Sequences of TCR-alpha and TCR-beta V(D)J Variable Regions
Targeted RNA-Seq for Capture of Full-Length Transcript Information—SMARTer Target RNA Capture for Illumina
ThruPLEX DNA-seq Kit—General Purpose Library Preparation for Illumina NGS Platforms
SMARTer PicoPLEX DNA-seq Kit—Single-Cell Library Preparation for Illumina NGS Platforms
Customizable Targeting of Key Oncology Variants Â
Interrogate clinically-relevant colorectal cancer genes
Expansive profiling of BRCA1, BRCA2 and PALB2 genes
