lexogen代理——北京百奧創新科技有限公司

QuantSeq Expression Profiling Library Prep Kits

QuantSeq kits enable cost-efficient RNA sequencing by counting. These kits are an exceptional alternative to standard whole-transcriptome RNA-Seq, microarrays or even qPCR. Just one fragment per transcript is produced and therefore there is no need for length normalization. This makes data analysis very simple, fast, and accurate. By using Lexogen’s i5 and i7 dual indices, up to 9,216 or even 36,864 (QuantSeq-Pool) samples can be multiplexed in one lane, saving your sequencing space. Moreover, unique 96 i5 x 96 i7 indices help detect and quantify index hopping and minimize mis-assignment. QuantSeq is available for 3’ mRNA-Seq and targeted RNA-Seq.

CORALL RNA-Seq Library Prep Kits

The CORALL RNA-Seq Library Prep Kits enables fast and cost-efficient generation of stranded, UMI labelled, and unique dual indexed libraries for whole transcriptome analyses using Illumina® NGS platforms. CORALL is the universal solution for all your samples offering exceptional performance on low input samples, down to 1 ng starting amount. It is the ideal solution for total RNA-Seq analysis on degraded and FFPE samples.

LUTHOR 3’ mRNA-Seq Library Prep Kit

LUTHOR combines the novel THOR (T7 High-resolution Original RNA) Amplification Technology with a highly efficient library preparation for 3’ mRNA-Seq analysis of one individual cell or ultra-low RNA input. It provides unprecedented sensitivity, reproducibility, and a reduction of systematic errors. This template-switch-, ligation- and fragmentation-free protocol enables RNA-Seq even from challenging individual, singularized cells.

TraPR Small RNA Isolation Kit

The TraPR Small RNA Isolation Kit isolates functional, physiologically relevant silencing sRNAs from any organism, tissue, cell type, or bio-fluid. In contrast to previous state-of-the-art methods, this innovative 15-minute single-column workflow neither requires prior knowledge of the sample, nor does it involve tedious gel extraction steps or lengthy immuno-precipitation procedures. TraPR thus enables the extraction of high-quality sRNAs even from challenging or uncharacterized material, leading to highly reproducible sequencing results.

Small RNA-Seq Library Prep Kit

Small RNA-Seq Library Prep Kit provides a protocol for generation of small RNA libraries for Illumina sequencing directly from total RNA or enriched small RNA.

SPLIT RNA Extraction Kit

The SPLIT RNA Extraction Kit enables fast and highly efficient extraction of high quality, high purity RNA from a broad range of biological samples, including cell culture, animal and plant tissue, and fluid samples. Thus the obtained RNA is ideal for seamless library preparation for Next Generation Sequencing and other demanding applications. SPLIT recovers the complete RNA size ranges, including small RNAs.

SLAMseq Metabolic RNA Labeling Kit for RNA-Seq

SLAMseq is a high-sensitivity method for time-resolved measurement of newly synthesized and existing RNA in cultured cells. SLAMseq enables resolution of RNA synthesis and degradation kinetics.

RiboCop rRNA Depletion Kits

RiboCop rRNA Depletion Kits for Human/Mouse/Rat for Bacteria, and Yeast enable removal of ribosomal RNA from total RNA and are suited for Next Generation Sequencing as well as other demanding RNA analysis applications.

TeloPrime Full-Length cDNA Amplification Kit V2

TeloPrime Full-Length cDNA Amplification Kit V2 generates full-length cDNA from total RNA. It is highly selective for full-length RNA molecules that are both capped and polyadenylated and therefore no cDNA from degraded RNA is being amplified. High-efficiency PCR produces excellent cDNA yields ideal for downstream long-read sequencing applications.

SIRVs (Spike-in RNA Variant Control Mixes)

The SIRVs are a set of transcript variants designed to assess RNA sequencing workflows for their performance in transcriptome analysis in categories such as detection of isoforms, linearity of dose response and sensitivity, and transcript length. This includes the testing of bioinformatic algorithms for their ability to quantify, map, and assemble isoforms. In addition to these validation applications, the SIRVs can function as “fingerprints" to assess concordance of RNA-Seq data sets.