The GS Junior Titanium emPCR Kit (Lib-A) provides reagents for the amplification of an Amplicon library from a single effective (i.e., functionally clonal) bead-bound copy of the DNA template to tens of millions of copies per bead, amenable to sequencing with the GS Junior Instrument using the appropriate GS Junior Titanium kits. One of the main advantages of the emPCR Amplification process is that, while the entire procedure…
The GS Junior Titanium emPCR Kit (Lib-L) provides reagents for the amplification of a Shotgun, Paired End or cDNA library from a single effective (i.e., functionally clonal) bead-bound copy of the DNA template to tens of millions of copies per bead, amenable to sequencing with the GS Junior Instrument using the appropriate GS Junior Titanium kits. One of the main advantages of the emPCR Amplification process is that, while the…
The GS FLX Titanium emPCR Kits (Lib-A) contain all reagents and other components required for two large-volume (LV), medium-volume (MV) or small-volume (SV) emulsion-based clonal amplifications of DNA libraries prepared using the Genome Sequencer System library preparation procedure (Amplicons), for subsequent sequencing on a Genome Sequencer FLX Instrument using the appropriate GS FLX Titanium series Sequencing and PicoTiterP…
Kits for large-volume (LV), medium-volume (MV) and small-volume (SV) emulsion-based clonal amplification of a DNA library prepared using the appropriate GS FLX Titanium series library preparation procedure. The GS FLX Titanium emPCR Kits (Lib-L) contain all reagents and other components required for two emulsion-based clonal amplification reactions (which can be pooled, if applicable). Contents The GS FLX Titanium emPCR Kits…
SURVEYOR Mutation Detection Kits provide a simple, accurate and cost-effective means to scan DNA fragments for mutations with unmatched sensitivity and specificity. The SURVEYOR Mutation Detection Kit for Standard Gel Electrophoresis has been designed to cleave unlabeled DNA fragments at mismatched sites for subsequent analysis by agarose gel electrophoresis or polyacrylamide gel electrophoresis (PAGE). DNA 200 to 4,000 bp lo…
The gold standard for NGS library amplification.
KAPA Library Quantification Kits contain all the reagents needed for the accurate, reliable and reproducible qPCR-based quantification of NGS libraries prior to pooling for capture or flow cell amplification. Kits contain KAPA SYBR® FAST qPCR Master Mix, optimized for high-performance SYBR Green I-based qPCR. The engineered KAPA SYBR FAST DNA Polymerase contained in the Master Mix amplifies GC- and AT-rich DNA fragments of…
Multiplex amplicon panels for Illumina® platform.
Multiplex amplicons for Illumina® platform.
Multiplex amplicon panels for Illumina® platform.
Simply track and manage samples within and between studies.
200 x 20 µl reactions, includes ddPCR Library Quantification Assay and ddPCR Supermix for Probes (No dUTP), for quantification of Illumina TruSeq libraries using the QX200™/QX100™ ddPCR™ Systems
NGS library prep for hybridization capture
NGS library prep for hybridization capture
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…
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.
Ion AmpliSeq HD technology is a new amplicon-based library preparation technology for Ion Torrent next-generation sequencing (NGS) that gives you the power to design your own panels and find variants with a low limit of detection—down to 0.1% for cell-free DNA samples. This revolutionary technology enables researchers to routinely get answers when ultrahigh sensitivity is required, such as when detecting low-frequency alleles…
Customizable Targeting of Key Oncology Variants
Interrogate clinically-relevant colorectal cancer genes
Sequence key genes implicated in Lynch Syndrome
Interrogate hematological malignancy genes
All-exon sequencing of TP53
