Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Various applications are leveraged to support cancer research workflows from molecular applications with PCR and NGS to imaging and flow cytometry. All these workflow applications begin with sample preparation. Thermo Fisher Scientific provides end-to-end oncology research solutions for liquid biopsy and solid tumor research including complimentary research of cells, proteins, and exosomes.
Answer a few short questions to uncover sample preparation solutions that fit your workflow needs.
Liquid biopsies examine biomarkers shed by tumors, such as circulating tumor cells, tumor DNA, or exosomes. They are less invasive than surgical biopsies and can detect cancer early, monitor treatment response, and identify therapy resistance.
Thermo Fisher Scientific offers sample preparation solutions for liquid biopsy research. Our MagMAX chemistry workflows on KingFisher instruments deliver accurate and reproducible results for detecting rare mutations in circulating tumor DNA and RNA. Dynabeads magnetic beads enable gentle isolation of intact exosomes and circulating tumor cells with high specificity and sensitivity.
Thermo Fisher Scientific products, including MagMAX, Dynabeads and KingFisher products, are essential tools for liquid biopsy research, helping to advance our understanding of cancer biology and improve translational patient outcomes.
High-quality cfDNA purification—MagMAX Cell-Free DNA Isolation Kit design allows for high-quality cfDNA yield and enrichment from plasma, serum, and urine.
High-quality cfTNA purification—MagMAX Cell-Free Total Nucleic Acid Kit is designed for the purification of DNA, RNA, and miRNA from plasma, serum, urine, and saliva.
Biomarker | Cell free nucleic acids | ||
---|---|---|---|
Product Click on the product names or images to learn more | KingFisher Apex | MagMAX Cell-Free Total Nucleic Acid Isolation Kit | MagMAX Cell-Free DNA Isolation Kit |
Sample type | RNA, DNA, protein, cells | Plasma, serum, urine | Plasma, serum, urine Now with expanded automation capabilities: saliva & large volume urine |
Isolation technology | Automated magnetic beads | Magnetic beads | Magnetic beads |
Downstream applications | RT-PCR, RT-qPCR, NGS, CE | RT-PCR, RT-qPCR, NGS, CE | RT-PCR, RT-qPCR, NGS |
Automation compatible | Yes | Yes | Yes |
Request a quote | Order now | Order now |
Qubit Fluorometers provide fast, accurate, and precise quantification of the DNA, RNA, or protein within a sample. The Qubit 4 and Qubit Flex Fluorometers use target-selective Qubit assays that fluoresce when bound specifically to the target molecules of interest. Learn how the quantification of these analytes is important for downstream applications like next generation sequencing (NGS), PCR, transfection, western blotting, and immunoassays.
Quickly quantify DNA, RNA, and protein using only 1–2 µL of sample with Thermo Scientific NanoDrop Spectrophotometers. Our pioneering sample-retention technology has evolved across the full spectrum to bring you more knowledge about your sample, so that you can save days of troubleshooting and accelerate your research.
Accurate, sensitive, and precise dPCR data with a master mix specifically formulated to enable analysis of higher sample volumes. Delivers accurate quantification of DNA targets without using a standard curve.
Enables reproducible, specific detection of known somatic mutations with wet-lab validated assays capable of detecting down to 0.1% variant allele frequency in genes relevant for cancer research.
Sensitive and precise digital PCR data can be collected in as little as 90 minutes with a simple one-step workflow.
Fully automates library preparation, template preparation, and produces sequencing-ready Ion Torrent semiconductor chips.
Efficiently capture DNA sequences of interest through specific hybridization via immobilization of target-specific biotinylated probes to streptavidin coated beads.
High performance cleanup and size selection beads designed to seamlessly integrate into existing workflows. Optimized to achieve >90% recovery of fragments larger than 90 bps. Added efficiency of ambient temperature storage and affordable pricing without compromising on performance.
Amplicon-based library preparation technology that gives you the power to design your own panels and find variants with a low limit of detection.
Identify known somatic mutations, CNVs, and fusion genes with targeted NGS assays that are tumor-type specific. Also simultaneously detect DNA and RNA variants across multiple cancer types.
Rapid, simultaneous detection of biomarkers across 50 genes from liquid biopsy samples, as well as solid tissue samples.
Rapidly and efficiently run small and large projects across multiple research applications, with a simple sample-to-data NGS workflow.
Get accurate results and reliable performance of Sanger sequencing and fragment analysis, while leveraging design improvements and technological advances for increased flexibility, easier operation, enhanced connectivity, and remote serviceability.
Optimized and streamlined kits to help you prepare samples for Sanger sequencing and fragment analysis applications on Applied Biosystems genetic analyzers. Our kits will help to keep your lab running at maximum efficiency.
A wide portfolio of Applied Biosystems software solutions for viewing and interpreting your Sanger sequencing and fragment analysis results.
Biomarker | Cell free nucleic acids | ||
---|---|---|---|
Product Click on the product names or images to learn more | KingFisher Apex | MagMAX Cell-Free Total Nucleic Acid Isolation Kit | MagMAX Cell-Free DNA Isolation Kit |
Sample type | RNA, DNA, protein, cells | Plasma, serum, urine | Plasma, serum, urine Now with expanded automation capabilities: saliva & large volume urine |
Isolation technology | Automated magnetic beads | Magnetic beads | Magnetic beads |
Downstream applications | RT-PCR, RT-qPCR, NGS, CE | RT-PCR, RT-qPCR, NGS, CE | RT-PCR, RT-qPCR, NGS |
Automation compatible | Yes | Yes | Yes |
Request a quote | Order now | Order now |
Qubit Fluorometers provide fast, accurate, and precise quantification of the DNA, RNA, or protein within a sample. The Qubit 4 and Qubit Flex Fluorometers use target-selective Qubit assays that fluoresce when bound specifically to the target molecules of interest. Learn how the quantification of these analytes is important for downstream applications like next generation sequencing (NGS), PCR, transfection, western blotting, and immunoassays.
Quickly quantify DNA, RNA, and protein using only 1–2 µL of sample with Thermo Scientific NanoDrop Spectrophotometers. Our pioneering sample-retention technology has evolved across the full spectrum to bring you more knowledge about your sample, so that you can save days of troubleshooting and accelerate your research.
Accurate, sensitive, and precise dPCR data with a master mix specifically formulated to enable analysis of higher sample volumes. Delivers accurate quantification of DNA targets without using a standard curve.
Enables reproducible, specific detection of known somatic mutations with wet-lab validated assays capable of detecting down to 0.1% variant allele frequency in genes relevant for cancer research.
Sensitive and precise digital PCR data can be collected in as little as 90 minutes with a simple one-step workflow.
Fully automates library preparation, template preparation, and produces sequencing-ready Ion Torrent semiconductor chips.
Efficiently capture DNA sequences of interest through specific hybridization via immobilization of target-specific biotinylated probes to streptavidin coated beads.
High performance cleanup and size selection beads designed to seamlessly integrate into existing workflows. Optimized to achieve >90% recovery of fragments larger than 90 bps. Added efficiency of ambient temperature storage and affordable pricing without compromising on performance.
Amplicon-based library preparation technology that gives you the power to design your own panels and find variants with a low limit of detection.
Identify known somatic mutations, CNVs, and fusion genes with targeted NGS assays that are tumor-type specific. Also simultaneously detect DNA and RNA variants across multiple cancer types.
Rapid, simultaneous detection of biomarkers across 50 genes from liquid biopsy samples, as well as solid tissue samples.
Rapidly and efficiently run small and large projects across multiple research applications, with a simple sample-to-data NGS workflow.
Get accurate results and reliable performance of Sanger sequencing and fragment analysis, while leveraging design improvements and technological advances for increased flexibility, easier operation, enhanced connectivity, and remote serviceability.
Optimized and streamlined kits to help you prepare samples for Sanger sequencing and fragment analysis applications on Applied Biosystems genetic analyzers. Our kits will help to keep your lab running at maximum efficiency.
A wide portfolio of Applied Biosystems software solutions for viewing and interpreting your Sanger sequencing and fragment analysis results.
Application note: A complete next-generation sequencing workflow for circulating cell-free DNA isolation and analysis
In this study, a complete targeted sequencing workflow is presented for mutation detection from cfDNA, involving the isolation of cfDNA from plasma, followed by molecular characterization using Ion AmpliSeq technology and the Ion PGM System.
Application note: Extraction and analysis of circulating cell-free DNA from plasma samples for lung cancer
In this study, we describe a method for extracting cfDNA from plasma samples of healthy donors and lung cancer patients using the Applied Biosystems MagMAX Cell-Free DNA Isolation Kit, followed by digital PCR and next-generation sequencing analysis, which saves compared to traditional methods.
Intact Exosome enrichment—Dynabeads Intact virus enrichment kit is designed for isolation of intact exosomes from plasma, serum, urine and cell culture.
Biomarker | Exosomes |
---|---|
Product Click on the product names or images to learn more | Dynabeads Intact Virus Enrichment |
Sample type | Plasma, serum, urine, cell culture |
Isolation technology | Magnetic beads |
Downstream applications | RT-PCR, RT-qPCR, NGS, Western, Immunoprecipitation, mass spectrometry |
Automation compatible | Yes |
Order now |
Application note: Bead based isolation of exosomes for multiomic research
Here we present a method for generic exosome isolation within 10 minutes using Invitrogen Dynabeads Intact Virus Enrichment magnetic beads. A panel of different methods was used to identify the isolated exosomes. Measurements of vesicle size and concentration were done by microfluidic resistive pulse sensing analysis.
CTC isolation—Dynabeads Epithelial Enrich is designed for positive isolation of circulating tumor cells from PBMC’s and whole blood. Dynabeads CD45 is designed for negative isolation of circulating tumor cells from PBMC’s and lysed whole blood through depletion of CD45+ leukocytes. Dynabeads MyOne CD45 is a highly efficient solution designed for depletion of human CD45 positive cells from whole blood, buffy coat, or peripheral blood mononuclear cells (PBMC). By discarding the bead-bound cells, the product allows for the utilization of the remaining untouched rare target cells in downstream applications.
Biomarker | Circulating tumor cells | ||
---|---|---|---|
Product Click on the product names or images to learn more | Dynabeads Epithelial Enrich | Dynabeads CD45 | Dynabeads MyOne CD45 Leukocyte Depletion |
Sample type | PBMC, blood | PBMC, blood | PBMC, Blood |
Isolation technology | Magnetic beads—positive cell isolation | Magnetic beads—negative cell isolation | Magnetic beads—improved performance negative cell isolation |
Downstream applications | RT-PCR, RT-qPCR, NGS, Western, Immunoprecipitation, mass spectrometry | RT-PCR, RT-qPCR, NGS, Western, Immunoprecipitation, mass spectrometry | RT-PCR, RT-qPCR, NGS, Western, Immunoprecipitation, mass spectrometry |
Automation compatible | Yes | Yes | Yes |
Order now | Order now | Order now |
Accurate, sensitive, and precise dPCR data with a master mix specifically formulated to enable analysis of higher sample volumes. Delivers accurate quantification of DNA targets without using a standard curve.
Enables reproducible, specific detection of known somatic mutations with wet-lab validated assays capable of detecting down to 0.1% variant allele frequency in genes relevant for cancer research.
Sensitive and precise digital PCR data can be collected in as little as 90 minutes with a simple one-step workflow.
Fully automates library preparation, template preparation, and produces sequencing-ready Ion Torrent semiconductor chips.
Efficiently capture DNA sequences of interest through specific hybridization via immobilization of target-specific biotinylated probes to streptavidin coated beads.
High performance cleanup and size selection beads designed to seamlessly integrate into existing workflows. Optimized to achieve >90% recovery of fragments larger than 90 bps. Added efficiency of ambient temperature storage and affordable pricing without compromising on performance.
Amplicon-based library preparation technology that gives you the power to design your own panels and find variants with a low limit of detection.
Identify known somatic mutations, CNVs, and fusion genes with targeted NGS assays that are tumor-type specific. Also simultaneously detect DNA and RNA variants across multiple cancer types.
Rapid, simultaneous detection of biomarkers across 50 genes from liquid biopsy samples, as well as solid tissue samples.
Rapidly and efficiently run small and large projects across multiple research applications, with a simple sample-to-data NGS workflow.
Biomarker | Circulating tumor cells | ||
---|---|---|---|
Product Click on the product names or images to learn more | Dynabeads Epithelial Enrich | Dynabeads CD45 | Dynabeads MyOne CD45 Leukocyte Depletion |
Sample type | PBMC, blood | PBMC, blood | PBMC, Blood |
Isolation technology | Magnetic beads—positive cell isolation | Magnetic beads—negative cell isolation | Magnetic beads—improved performance negative cell isolation |
Downstream applications | RT-PCR, RT-qPCR, NGS, Western, Immunoprecipitation, mass spectrometry | RT-PCR, RT-qPCR, NGS, Western, Immunoprecipitation, mass spectrometry | RT-PCR, RT-qPCR, NGS, Western, Immunoprecipitation, mass spectrometry |
Automation compatible | Yes | Yes | Yes |
Order now | Order now | Order now |
Accurate, sensitive, and precise dPCR data with a master mix specifically formulated to enable analysis of higher sample volumes. Delivers accurate quantification of DNA targets without using a standard curve.
Enables reproducible, specific detection of known somatic mutations with wet-lab validated assays capable of detecting down to 0.1% variant allele frequency in genes relevant for cancer research.
Sensitive and precise digital PCR data can be collected in as little as 90 minutes with a simple one-step workflow.
Fully automates library preparation, template preparation, and produces sequencing-ready Ion Torrent semiconductor chips.
Efficiently capture DNA sequences of interest through specific hybridization via immobilization of target-specific biotinylated probes to streptavidin coated beads.
High performance cleanup and size selection beads designed to seamlessly integrate into existing workflows. Optimized to achieve >90% recovery of fragments larger than 90 bps. Added efficiency of ambient temperature storage and affordable pricing without compromising on performance.
Amplicon-based library preparation technology that gives you the power to design your own panels and find variants with a low limit of detection.
Identify known somatic mutations, CNVs, and fusion genes with targeted NGS assays that are tumor-type specific. Also simultaneously detect DNA and RNA variants across multiple cancer types.
Rapid, simultaneous detection of biomarkers across 50 genes from liquid biopsy samples, as well as solid tissue samples.
Rapidly and efficiently run small and large projects across multiple research applications, with a simple sample-to-data NGS workflow.
Application note: Isolation of circulating tumor cells using Dynabeads magnetic beads
Invitrogen Dynabeads magnetic beads provide an automation-friendly tool for isolation of circulating biomarkers. Here we evaluate Dynabeads magnetic beads for feasibility in both positive and negative CTC isolation workflows.
Solid tumors are heterotypic aggregates of many cell types, including cancer cells, cancer stem cells, connective-tissue cells, and immune cells. Common sample types used to begin cancer research and detection include fresh-frozen (FF) or formalin-fixed paraffin-embedded (FFPE) sample tissues. These are obtained through biopsy or excision of the malignant mass.
Sequential extraction—MagMAX FFPE DNA/RNA Ultra Kit allows sequential isolation of DNA and RNA from the same formalin-fixed, paraffin-embedded (FFPE) tissue sample.
Accurate and reproducible downstream results—MagMAX and Purelink kits for solid tumor nucleic acid purification are designed with optimized protocols and reagents for maximum yield and purity, helping ensure high-quality input for downstream applications.
Click through workflow steps for more information.
Process formalin-fixed paraffin-embedded (FFPE) tissue samples for high-quality nucleic acid isolation and simplify deparaffinization. AutoLys M Tubes eliminate the need for solvent based deparaffinization and extensive hands on time for sample preprocessing.
AutoLys M | AutoLys M | AutoLys M | AutoLys M | AutoLys M | |
Description | AutoLys M Tubes are for the preparation of FFPE samples for nucleic acid extraction. They feature a novel tube-in-tube design that creates cleared lysates from FFPE tissue samples, without the need for tedious and harmful chemical-based deparaffinization or wash steps, while increasing DNA and RNA yields by minimizing sample loss. | The AutoLys M TubeLifter enables a rack of 24 AutoLys M Tubes to be simultaneously “lifted” and readied for centrifugation. Once centrifugation is complete, the rack of tubes is returned to the TubeLifter and the inner tube of each AutoLys M Tube is separated from the outer tube. | The AutoLys M Tube Locking lid is included with purchase of the AutoLys M TubeLifter. The locking lid is required to prevent the inner tube of the AutoLys M Tube from sliding into the outer tube during centrifugation. | AutoLys M Tube Racks hold 24 AutoLys M Tubes per rack. The racks are locked and unlocked using the AutoLys M TubeLifter or the AutoLys M Tube Pliers. | AutoLys M Tube Pliers can be used to separate the inner-tube from the outer-tube of AutoLys M Tubes. AutoLys M Tube Pliers can be used to separate the outer-tube of AutoLys M Tubes individually. After centrifugation, the outer-tube will contain the lysate that is processed further to recover nucleic acid within the MagMAX FFPE DNA/RNA Ultra kit workflows. |
Sample types | FFPE curls, FFPE blocks | ||||
Order now | Order now | Order now | Order now | Order now |
We offer multiple solutions for extracting nucleic acid from solid tumor samples. Our kits are designed to provide maximum yield, purity, and integrity so that your purified nucleic acid can be used in a variety of downstream applications.
Product Click on the product names or images to learn more | KingFisher Apex | MagMAX FFPE DNA/RNA Ultra Kit | MagMAX DNA Multi-Sample Ultra 2.0 Kit | MagMAX mirVana Total RNA Isolation Kit | PureLink FFPE RNA Isolation Kit |
Sample type | RNA, DNA, protein, cells | FFPE tissue samples | Multiple, including whole blood, swabs, tissue, and more Now with expanded automation capabilities: bone marrow & large volume blood. | Blood, cells, liquid samples (e.g., serum), RNA, tissue | FFPE tissue samples |
Isolation technology | Automated magnetic beads | Magnetic beads | Magnetic beads | Magnetic beads | Silica spin column |
Downstream applications | RT-PCR, RT-qPCR, NGS, western workflow | RT-PCR, RT-qPCR, NGS, microRNA analysis | RT-PCR, RT-qPCR, NGS, microarray analysis | RT-PCR, RT-qPCR, NGS, microRNA analysis | Microarray analysis, RT-qPCR, RT-PCR, northern blotting, cDNA library construction |
Automation compatible | Yes | Yes | Yes | Yes | No |
Request a quote | Order now | Order now | Order now | Order now |
Qubit Fluorometers provide fast, accurate, and precise quantification of the DNA, RNA, or protein within a sample. The Qubit 4 and Qubit Flex Fluorometers use target-selective Qubit assays that fluoresce when bound specifically to the target molecules of interest. Learn how the quantification of these analytes is important for downstream applications like next generation sequencing (NGS), PCR, transfection, western blotting, and immunoassays.
Quickly quantify DNA, RNA, and protein using only 1–2 µL of sample with Thermo Scientific NanoDrop Spectrophotometers. Our pioneering sample-retention technology has evolved across the full spectrum to bring you more knowledge about your sample, so that you can save days of troubleshooting and accelerate your research.
Accurate, sensitive, and precise dPCR data with a master mix specifically formulated to enable analysis of higher sample volumes. Delivers accurate quantification of DNA targets without using a standard curve.
Sensitive and precise digital PCR data can be collected in as little as 90 minutes with a simple one-step workflow.
Fully automates library preparation, template preparation, and produces sequencing-ready Ion Torrent semiconductor chips.
Efficiently capture DNA sequences of interest through specific hybridization via immobilization of target-specific biotinylated probes to streptavidin coated beads.
High performance cleanup and size selection beads designed to seamlessly integrate into existing workflows. Optimized to achieve >90% recovery of fragments larger than 90 bps. Added efficiency of ambient temperature storage and affordable pricing without compromising on performance.
Thermo Fisher Scientific offers a wide range of solutions for solid tumor research and detection. Browse our Oncomine Assays and tumor-specific panels and find the right products to meet your specific tumor research needs.
Customizable, automated sequencing data analysis.
Fast, simple variant calling and annotation of SNPs, indels, CNVs, and fusions.
Summarize relevant cancer drivers in a simple report that links sample-specific variants to labels, guidelines, and current global clinical trials.
Get accurate results and reliable performance of Sanger sequencing and fragment analysis, while leveraging design improvements and technological advances for increased flexibility, easier operation, enhanced connectivity, and remote serviceability.
Optimized and streamlined kits to help you prepare samples for Sanger sequencing and fragment analysis applications on Applied Biosystems genetic analyzers. Our kits will help to keep your lab running at maximum efficiency.
A rapid and compatible workflow that has a panel of 13 microsatellite markers to test for MSI associated with Lynch syndrome-related cancers beyond colorectal cancer and studying immunotherapy.
A wide portfolio of Applied Biosystems software solutions for viewing and interpreting your Sanger sequencing and fragment analysis results.
Process formalin-fixed paraffin-embedded (FFPE) tissue samples for high-quality nucleic acid isolation and simplify deparaffinization. AutoLys M Tubes eliminate the need for solvent based deparaffinization and extensive hands on time for sample preprocessing.
AutoLys M | AutoLys M | AutoLys M | AutoLys M | AutoLys M | |
Description | AutoLys M Tubes are for the preparation of FFPE samples for nucleic acid extraction. They feature a novel tube-in-tube design that creates cleared lysates from FFPE tissue samples, without the need for tedious and harmful chemical-based deparaffinization or wash steps, while increasing DNA and RNA yields by minimizing sample loss. | The AutoLys M TubeLifter enables a rack of 24 AutoLys M Tubes to be simultaneously “lifted” and readied for centrifugation. Once centrifugation is complete, the rack of tubes is returned to the TubeLifter and the inner tube of each AutoLys M Tube is separated from the outer tube. | The AutoLys M Tube Locking lid is included with purchase of the AutoLys M TubeLifter. The locking lid is required to prevent the inner tube of the AutoLys M Tube from sliding into the outer tube during centrifugation. | AutoLys M Tube Racks hold 24 AutoLys M Tubes per rack. The racks are locked and unlocked using the AutoLys M TubeLifter or the AutoLys M Tube Pliers. | AutoLys M Tube Pliers can be used to separate the inner-tube from the outer-tube of AutoLys M Tubes. AutoLys M Tube Pliers can be used to separate the outer-tube of AutoLys M Tubes individually. After centrifugation, the outer-tube will contain the lysate that is processed further to recover nucleic acid within the MagMAX FFPE DNA/RNA Ultra kit workflows. |
Sample types | FFPE curls, FFPE blocks | ||||
Order now | Order now | Order now | Order now | Order now |
We offer multiple solutions for extracting nucleic acid from solid tumor samples. Our kits are designed to provide maximum yield, purity, and integrity so that your purified nucleic acid can be used in a variety of downstream applications.
Product Click on the product names or images to learn more | KingFisher Apex | MagMAX FFPE DNA/RNA Ultra Kit | MagMAX DNA Multi-Sample Ultra 2.0 Kit | MagMAX mirVana Total RNA Isolation Kit | PureLink FFPE RNA Isolation Kit |
Sample type | RNA, DNA, protein, cells | FFPE tissue samples | Multiple, including whole blood, swabs, tissue, and more Now with expanded automation capabilities: bone marrow & large volume blood. | Blood, cells, liquid samples (e.g., serum), RNA, tissue | FFPE tissue samples |
Isolation technology | Automated magnetic beads | Magnetic beads | Magnetic beads | Magnetic beads | Silica spin column |
Downstream applications | RT-PCR, RT-qPCR, NGS, western workflow | RT-PCR, RT-qPCR, NGS, microRNA analysis | RT-PCR, RT-qPCR, NGS, microarray analysis | RT-PCR, RT-qPCR, NGS, microRNA analysis | Microarray analysis, RT-qPCR, RT-PCR, northern blotting, cDNA library construction |
Automation compatible | Yes | Yes | Yes | Yes | No |
Request a quote | Order now | Order now | Order now | Order now |
Qubit Fluorometers provide fast, accurate, and precise quantification of the DNA, RNA, or protein within a sample. The Qubit 4 and Qubit Flex Fluorometers use target-selective Qubit assays that fluoresce when bound specifically to the target molecules of interest. Learn how the quantification of these analytes is important for downstream applications like next generation sequencing (NGS), PCR, transfection, western blotting, and immunoassays.
Quickly quantify DNA, RNA, and protein using only 1–2 µL of sample with Thermo Scientific NanoDrop Spectrophotometers. Our pioneering sample-retention technology has evolved across the full spectrum to bring you more knowledge about your sample, so that you can save days of troubleshooting and accelerate your research.
Accurate, sensitive, and precise dPCR data with a master mix specifically formulated to enable analysis of higher sample volumes. Delivers accurate quantification of DNA targets without using a standard curve.
Sensitive and precise digital PCR data can be collected in as little as 90 minutes with a simple one-step workflow.
Fully automates library preparation, template preparation, and produces sequencing-ready Ion Torrent semiconductor chips.
Efficiently capture DNA sequences of interest through specific hybridization via immobilization of target-specific biotinylated probes to streptavidin coated beads.
High performance cleanup and size selection beads designed to seamlessly integrate into existing workflows. Optimized to achieve >90% recovery of fragments larger than 90 bps. Added efficiency of ambient temperature storage and affordable pricing without compromising on performance.
Thermo Fisher Scientific offers a wide range of solutions for solid tumor research and detection. Browse our Oncomine Assays and tumor-specific panels and find the right products to meet your specific tumor research needs.
Customizable, automated sequencing data analysis.
Fast, simple variant calling and annotation of SNPs, indels, CNVs, and fusions.
Summarize relevant cancer drivers in a simple report that links sample-specific variants to labels, guidelines, and current global clinical trials.
Get accurate results and reliable performance of Sanger sequencing and fragment analysis, while leveraging design improvements and technological advances for increased flexibility, easier operation, enhanced connectivity, and remote serviceability.
Optimized and streamlined kits to help you prepare samples for Sanger sequencing and fragment analysis applications on Applied Biosystems genetic analyzers. Our kits will help to keep your lab running at maximum efficiency.
A rapid and compatible workflow that has a panel of 13 microsatellite markers to test for MSI associated with Lynch syndrome-related cancers beyond colorectal cancer and studying immunotherapy.
A wide portfolio of Applied Biosystems software solutions for viewing and interpreting your Sanger sequencing and fragment analysis results.
Dynabeads magnetic beads enable higher-throughput applications for which samples can be processed in 24- or 96-well plates on the KingFisher family of instruments. Sample types include RNA, DNA, proteins, cells and exosomes.
Comparison of DNA and RNA from fresh-frozen vs. FFPE tissue samples
Mutation detection sensitivity in matched FFPE tissue and liquid biopsy samples
A convenient, solvent-free deparaffinization method for FFPE sample preparation
For Research Use Only. Not for use in diagnostic procedures.