FusionPlex Pan Solid V2 is a research assay for targeted next generation sequencing of RNA for characterization of variants, indels, and fusions, including novel fusions, from 137 genes associated with various solid tumor malignancies.
VariantPlex Solid Tumor Focus V2 is a research assay for targeted next generation sequencing of DNA for characterization of SNVs, indels, CNVs, and MSI from 20 genes associated with various solid tumor malignancies.
VariantPlex Core Solid Tumor is a research assay for targeted next generation sequencing of DNA for characterization of SNVs, indels, CNVs, and MSI from 60 genes associated with various solid tumor malignancies.
VariantPlex Expanded Solid Tumor is a research assay for targeted next generation sequencing of DNA for characterization of SNVs, indels, CNVs, and MSI from 76 genes associated with various solid tumor malignancies.
VariantPlex Pan Solid Tumor is a research assay for targeted next generation sequencing of DNA for characterization of SNVs, indels, CNVs, MSI, and TMB from 185 genes associated with various solid tumor malignancies.
VariantPlex Complete Solid Tumor is a research assay for targeted next generation sequencing of DNA for characterization of SNVs, indels, CNVs, MSI, and TMB from 430 genes associated with various solid tumor malignancies.
Immunoverse is a research assay that characterizes the immune repertoire, including assessment of T- and B-cell clonalities and rare clones, and detection of tumor infiltrating lymphocytes (TIL) and somatic hypermutation with targeted NGS of key T cell receptor and B cell receptor chain RNA relevant for blood cancer and solid tumor research.
VariantPlex Myeloid is a research assay for targeted next generation sequencing of DNA for characterization of SNVs, indels, CNVs, and ITDs from 75 genes associated with acute myeloid leukemia (AML), myeloproliferative neoplasms (MPN), myelodysplastic syndromes (MDS).
VariantPlex Core Myeloid is a research assay for targeted next generation sequencing of DNA for characterization of SNVs, indels, CNVs, and ITDs from 37 genes associated with acute myeloid leukemia (AML), myeloproliferative neoplasms (MPN), myelodysplastic syndromes (MDS).
FusionPlex Pan Heme is a research assay for targeted next generation sequencing of RNA for characterization of variants, indels, expression, and fusions, including novel fusions, from 199 genes associated with lymphoid and myeloid malignancies.
FusionPlex Heme V2 is a research assay for targeted next generation sequencing of RNA for characterization of variants, indels, expression, and fusions, including novel fusions, from 87 genes associated with lymphoid and myeloid malignancies.
FusionPlex Myeloid is a research assay for targeted next generation sequencing of RNA for characterization of variants, indels, expression, and fusions, including novel fusions, from 84 genes associated with myeloid-origin malignancies.
FusionPlex Lymphoma is a research assay for targeted next generation sequencing of RNA for characterization of variants, indels, expression, and fusions, including novel fusions, from 125 genes associated with lymphomas.
FusionPlex ALL is a research assay for targeted next generation sequencing of RNA for characterization of variants, indels, expression, and fusions, including novel fusions, from 81 genes associated with acute lymphoblastic leukemia (ALL) .
A comprehensive kit for efficient multiplex RT-qPCR in a single reaction tube. Ideal for multiplex (4-5) assays using dual-labelled hydrolysis probes, works with standard and fast cycling.
A comprehensive kit for performing dye-based RT-qPCR swiftly and reliably in a single tube. No carryover contamination and compatible with standard and fast cycling.
Reliable multiplex qPCR kit. Optimised for amplifying low copy DNA targets. Ideal for multiplexed reactions of 4 or 5 targets without compromising performance.
Ideal for quantification of any DNA template (gDNA, cDNA, viral DNA), amplifies low copy number samples with ease. Utilises our intercalating fluorescent dye, MicroGREEN, that binds to double stranded DNA, making it the perfect choice for qPCR & melt curve analysis.
This 2X concentrated format can be used with a broad range of templates and conditions for end point and qPCR with addition of a dye such as MicroGREEN or single plex probe assays. Easy set up and PCR optimisation plus extremely stable with the ability to be freeze thawed many times.
In-depth understanding of complete genome in human, aninal, plant and microbe with end-to-end services.
Sequencing only service for customer-premade libraries at different read lengths and capacities to suit any cost, project scale and turnaround with the world-leading, powerful, and sophisticated sequencing platforms (Illumina, Pacbio, and Oxford Nanopore).
16S/18S/ITS rRNA amplicon metagenomic sequencing employs universal primers to target specific regions to identify the phylogeny and taxonomy from complex microbiomes.
Single cell RNA sequencing uncovers the complexity of cellular diversity to employ the study of unusual cell types, cell-lineage associations, and samples of heterogeneous nature with 10x Genomics technology.
Phase Separator is a unique, new pipetting capability on the Fluent® Automation Workstation. This patented liquid separation technology can detect liquid-liquid interfaces and effectively separate neighbor phases while avoiding contamination. Suitable for removing the plasma phase from a centrifuged blood sample, it delivers up to double the speed of camera-based systems for plasma separation.
Derivatization is often used to visualize specific substance classes after separation on HPTLC glass plates (20 x 10 cm). Due to its unique and patented “micro droplet” spraying technology, the fully-automated HPTLC PRO Module DERIVATIZATION ensures homogeneity and reproducibility in applying derivatization reagents.
