Oligo Pools

PRODUCTS

Oligo Pools

Oligo Pools

Twist Oligo Pools represent collections of single-stranded oligonucleotides synthesized using state-of-the-art silicon-based DNA writing technology. The innovative synthesis platform employed by Twist Bioscience allows for the simultaneous production of large quantities of high-quality and accurate oligos in each run. This capability facilitates the creation of complex and diverse oligo pools, specifically advantageous for applications such as CRISPR screening.

The process involves users submitting their oligo sequences to Twist Bioscience, which then synthesizes user-designed oligo pool libraries. This service enables researchers to dedicate their time to experimental work and discovery, with the synthesis handled by Twist.

The quality of Twist oligos is underscored by highly uniform synthesis, as evidenced by Next-Generation Sequencing (NGS) quality control data. A representative oligo pool containing 23,000 90mer oligos demonstrates remarkable uniformity, with the corresponding table indicating the metrics for this pool. Twist oligos are synthesized with minimal bias, ensuring high uniformity and complete representation of oligos in the pool.

Furthermore, sequencing analysis of Oligo Pools generated by Twist Bioscience is compared with those from an array-based competitor. The results highlight the superiority of Twist Oligo Pools, as they consistently contain 100% of the expected sequences and exhibit a higher percentage of correct sequences when compared to the competitor’s pool. This emphasis on accuracy and completeness in sequence representation makes Twist Oligo Pools a robust and reliable choice for various molecular biology applications.

Oligo Pools Workflow
Oligo-Pools-Read-Counts-Histogram-Uniformity
Oligo-Pools-Sequencing-Analysis
New Cloned Oligo Pools

New Cloned Oligo Pools from Twist Bioscience represent a cutting-edge solution aimed at ensuring the foundational quality of oligo pools for successful experiments. Recognizing that errors during synthesis or cloning can adversely impact oligo pool quality by causing over and underrepresentation of desired sequences, Twist now provides an optimized cloning service. This service streamlines the experimental process by alleviating the need for researchers to navigate challenges such as testing PCR amplification conditions, selecting appropriate polymerases and primer pairs, and designing a cloning workflow.

The process involves just two steps. Users submit their oligo sequences to Twist Bioscience, and the company takes care of synthesizing, amplifying, and cloning the user-designed oligo pool libraries. This approach allows researchers to dedicate their time to experimentation and discovery while outsourcing the intricacies of oligo pool synthesis and cloning to Twist Bioscience.

Twist Bioscience emphasizes the high quality of its cloned oligo pools across all lengths, showcasing performance data for pools under 150 nucleotides and those up to 300 nucleotides in length, even with high GC content. The data highlight the uniformity achieved in both cases.

Twist’s cloned oligo pools not only exhibit low error rates and high uniformity but also boast low chimera rates. Chimeras, unwanted hybrid molecules resulting from suboptimal PCR conditions, can lead to improper amplification and recombination of different oligos within the pool. Twist Bioscience provides an illustration comparing an on-target cloned pool without chimeras to an off-target one containing chimeras, emphasizing the importance of avoiding undesired sequences.

The company asserts that its cloned oligo pools, free from chimeras, guarantee the highest quality and accuracy in experimental data. Comparative data between traditional amplification and Twist’s in-house amplification method further supports the efficacy of Twist’s approach in ensuring the integrity of oligo pools for diverse molecular biology applications.

Uniformity of linear and cloned oligo pools_0
edited-High quality cloned oligo pools
cloned Oligo-Pools-Sequencing-Analysis_0
Cloned oligo pools chimera
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    Other Panels

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    Other Panels

    Mitochondrial Panel

    The mitochondrial genome encodes factors critical to energy production, which directly affects the energy state of the cell, tissue, and human individual. Pathogenic mutations of Mitochondrial DNA (mtDNA) are often implicated in a group of complex human diseases which can be difficult to diagnose such as metabolic & neurologic disorders as well as cancer. Interrogation of the human mitochondrial genome by targeted Next Generation Sequencing (NGS) can help investigators shed light on the genetic mechanism behind mitochondrial disorders. 

    The Twist Mitochondrial Panel is a fixed content panel designed to cover all 16,659 base pairs (bp) and 37 genes of the mitochondrial genome. This panel can be used as a standalone panel or as a spike-in with Twist’s Human Core Exome, Comprehensive Exome as well as Twist’s Custom Panels. Providing industry-leading coverage, uniformity, and flexibility, the Twist Mitochondrial Panel can help investigators enrich for, sequence, and analyze mtDNA variants contributing to disease including incidences of heteroplasmy.

    Mitochondrial panel
    Twist Alliance Diversity SNP Panel

    Historical genotyping tools have long grappled with biases toward a limited number of ethnicities, resulting in underrepresentation of significant portions of the global population. Traditional platforms, like microarrays, exacerbate this issue by offering fixed content updated only periodically. To address these inefficiencies and promote equity, researchers can turn to target capture-based Next-Generation Sequencing (NGS) workflows with probe panels designed for diversity and flexibility.

    Twist’s expanding Targeted Genomic Block Sequencing (GBS) portfolio includes the Twist Diversity SNP Panel, offering a flexible, ethnicity-neutral gold standard for genotyping. This panel can be used independently or as a spike-in with the Twist Human Comprehensive Exome panel. Its customizable design allows for additional probes to cover specific regions of interest, all synthesized on Twist’s DNA synthesis platform.

    Developed in collaboration with the Regeneron Genetics Center, the Twist Diversity SNP Panel seamlessly integrates into existing fully automated exome processing workflows, providing base calls and imputed variants. Genotype imputations can be calculated using open-source tools, with an imputation guide available from Twist Customer Support for those starting with imputation analysis tools.

    Note: While the Diversity SNP panel content has not been fully validated through the complete Twist workflow, users are encouraged to contact Twist Customer Support for recommendations on assay set-up.

    Twist Alliance Pan-cancer Methylation Panel - 1.5 MB

    Methylation sequencing plays a crucial role in detecting and tracing the origins of cancer cells, offering sensitivity in unraveling complex methylation patterns. The Twist Alliance Pan-cancer Methylation Panel – 1.5 MB, a collaborative effort between Twist and AnchorDx, is tailored to focus on cancer-specific methylation patterns across 31 different cancers. This custom target enrichment panel provides deep coverage of clinically relevant targets, enabling the study of methylation patterns crucial for early cancer detection and diagnosis, especially from tumor and liquid biopsy samples.

    Constructed with Twist’s state-of-the-art oligonucleotide synthesis platform, the panel boasts high on-target rates and uniformity. It has undergone validation with the Twist Methylation workflow, utilizing liquid biopsy samples from breast cancer, colorectal cancer, and non-small cell lung cancer. The panel design, based on the TCGA database, covers 31 cancer types and 47 disease entities, featuring 13,090 probes targeting approximately 126k CpG sites. Notably, around 74% of the 12k differentially methylated regions (DMRs) overlap with CpG islands, showcasing the panel’s comprehensive coverage.

    It’s essential to note that the Twist Alliance Pan-cancer Methylation Panel – 1.5 MB does not carry ISO-13485 certification.

    Twist Alliance CNTG Exome - 41 MB

    The Twist Alliance CNTG Exome – 41 MB, developed through collaboration between CENTOGENE and Twist, serves as a powerful tool for addressing the challenges associated with the diagnosis of rare diseases. Rare diseases often pose difficulties for physicians, leading patients on prolonged diagnostic journeys. DNA sequencing panels, such as this collaboration, offer comprehensive solutions, providing answers and resolutions for patients undergoing these diagnostic odysseys.

    As a leader in rare disease diagnostics, CENTOGENE leverages its expertise in conjunction with Twist’s advanced omics technology to design target enrichment capture panels. The Twist Alliance CNTG Exome – 41 MB ensures highly uniform coverage of the entire exome, including full coverage of the mitochondrial genome. This panel significantly enhances diagnostic yield compared to standard whole exome sequencing, addressing a broad spectrum of disorders encompassing over 7,000 rare diseases.

    The panel comprises a total of 483,000 probes, with components such as the Twist Human Comprehensive Exome (396.1K probes), Twist Mitochondrial Panel (139 probes), Twist Alliance Centogene Rare Disease Panel (78.8K probes), and Centogene Spike-In (7.8K probes). Notably, the Twist Alliance CNTG Exome – 41 MB does not carry ISO-13485 certification, emphasizing its designation for research use only and not for diagnostic procedures.

    Twist Alliance CNTG Rare Disease Panel - 7.6 MB

    The Twist Alliance CNTG Rare Disease Panel, designated for research use only and not for diagnostic procedures, focuses on providing a more streamlined solution for researchers targeting rare diseases. With over 2,500 relevant genes associated with rare diseases, this panel ensures comprehensive coverage, encompassing ≥99.5% of targeted regions within the CNTG Exome footprint.

    Containing 78.8K probes, the Twist Alliance CNTG Rare Disease Panel is designed to detect genes linked to various conditions, including rare treatable diseases, early onset childhood disorders, cardiac disorders, neurodegenerative diseases, skeletal abnormalities, and metabolic disorders. This lightweight tool offers researchers the flexibility to capture crucial rare disease coverage without the full exome footprint.

    It’s important to note that the Twist Alliance CNTG Rare Disease Panel-7.6MB does not carry ISO-13485 certification, emphasizing its specific designation for research purposes.

    Twist Alliance CNTG Hereditary Oncology Panel - 0.2 MB

    The Twist Alliance CNTG Hereditary Oncology Panel, expressly designed for research use only and not intended for diagnostic procedures, focuses on providing a targeted solution for identifying genetic predisposition to hereditary tumors. This panel includes 72 carefully selected cancer-associated genes and covers ≥99.5% of targeted regions.

    With applications ranging from identifying genetic predispositions in breast cancer to gastrointestinal tumors, Li-Fraumeni syndrome, MEN1, MEN2, paragangliomas, and more, the Twist Alliance CNTG Hereditary Oncology Panel offers a specialized tool for researchers delving into the genetic underpinnings of hereditary cancers.

    It’s essential to note that the Twist Alliance CNTG Hereditary Oncology Panel- 0.2MB does not carry ISO-13485 certification and is exclusively designated for research purposes.

    Twist Human Ancient DNA Panel

    The Ancient Human DNA Panel, a collaborative effort with David Reich’s lab at Harvard University, is designed for studying genetic variation in ancient DNA specimens, typically obtained from bones and teeth. Targeting 1.35 million SNPs, this panel includes a subset covering all 1.23 million polymorphic sites in the human genome published in Fu et al. Nature 2015. This ensures compatibility with published data on numerous ancient individuals, fostering broad comparability.

    Developed using Twist’s double-stranded capture probes and hybridization capture reagents, the panel demonstrates high genome coverage and reduced allelic bias. This optimization, as highlighted in Rohland, Mallick et al. Genome Research 2022, enables genome-scale data at significantly reduced sequencing costs compared to shotgun sequencing, thanks to the highly efficient enrichment of human DNA fragments.

    It’s important to note that the Twist Alliance Ancient Human DNA Panel is not ISO-13485 certified, emphasizing its exclusive use for research purposes.

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    NGS Portfolio

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      R1 Cartridge BiOptic

      RNA Cartridges

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      RNA Cartridges

      RNA Cartridges

      R1 RNA Cartridge Kit

      1. The cartridge is ideal for low concentration RNA analysis and the analysis time is between 5~7 minutes.
      2. The system provides RNA Quality Number (RQN) for total RNA integrity reference.
      3. Each cartridge can analyze 100 runs for single-channel cartridge or 400 runs for 4-channel cartridge.
      4. The cartridge can be stored at room temperature (15~27°C) and is valid for 4 months.
      R1 Cartridge BiOptic

      NR1 High Sensitivity RNA Cartridge Kit

      1. The cartridge is ideal for low concentration RNA analysis (LOD 1 ng/μl) and the analysis time is between 5~7 minutes.
      2. The system provides RNA Quality Number (RQN) for total RNA integrity reference.
      3. Each cartridge can analyze 100 runs for single-channel cartridge or 400 runs for 4-channel cartridge.
      4. The cartridge can be stored at room temperature (15~27°C) and is valid for 4 months.
      NR1 Cartridge BiOptic
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        High Resolution Quantitative Cartridge Kit BiOptic

        Quantification Kit

        PRODUCTS

        Quantitative Kit

        Quantitative Kit

        S2 Standard Quantitative Cartridge Kit

        1. The fragment sizes and relatively accurate quantitative results can be obtained simultaneously. Extra time and cost for quantitative analysis can be saved.
        2. S2 cartridge is for PCR products, small-sized DNA, and NGS quality control (Fragmentation and Library sample) analyses.
        3. The analysis time is about 3 minutes, and the best resolution is 4~10bp if the sample size is less than 500bp.
        4. Each cartridge can analyze 200 runs for single-channel cartridge or 800 runs for 4-channel cartridge.
        5. The cartridge can be stored at 4~27°C and is valid for 6 months.
        Standard Quantitative Cartridge Kit BiOptic

        S1 High Resolution Quantitative Cartridge Kit

        1. The fragment sizes and relatively accurate quantitative results can be obtained simultaneously. Extra time and cost for quantitative analysis can be saved.
        2. Not only the total concentration but also the individual fragment concentration can be provided.
        3. The analysis time is about 3~5 minutes, and the best resolution is 1~4bp if the sample size is less than 500bp.
        4. Each cartridge can analyze 200 runs for single-channel cartridge or 800 runs for 4-channel cartridge.
        5. The cartridge can be stored at 4~27°C and is valid for 6 months.
        High Resolution Quantitative Cartridge Kit BiOptic

        N1 High Sensitivity Quantitative Cartridge Kit

        1. The fragment sizes and relatively accurate quantitative results of low concentration DNA can be obtained simultaneously with individual fragment concentration provided.
        2. The applications include low concentration DNA fragments and cell-free DNA quality control.
        3. The analysis takes about 3 minutes with a recommended size range up to around 5,000bp and a detection limit of about 10 pg/μl.
        4. Each cartridge can analyze 100 runs for single-channel cartridge or 400 runs for 4-channel cartridge.
        5. The cartridge can be stored at 4~27°C and is valid for 4 months.
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        BiOptic Consumables Portfolio

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          P2 Cartridge BiOptic

          Protein Cartridges

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          Protein Cartridges

          Protein Cartridges

          P2 Protein Cartridge Kit

          1. The cartridge analyzes protein sample size and purity with higher sensitivity and resolution.
          2. The analysis size range is 11~155kDa but the detection range is up to 600kDa.
          3. Qsep100 Advance is the recommended platform for detecting fluorescent-labeled protein sample.
          4. Each cartridge can analyze 100 runs for single-channel cartridge or 400 runs for 4-channel cartridge.
          P2 Cartridge BiOptic
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            S2 Cartridge (Standard Cartridge) BiOptic

            DNA Cartridges

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            DNA Cartridges

            DNA Cartridges

            S2 Standard Cartridge Kit

            1. S2 cartridge is for PCR products, small-sized DNA, and NGS quality control (Fragmentation and Library sample) analyses.
            2. The analysis time is 2~3 minutes and the best resolution is 4~10bp if the sample size is less than 500bp.
            3. It has a recommended size range up to around 5,000bp and a detection limit of about 0.1 ng/μl in low concentration.
            4. Each cartridge can analyze 200 runs for single-channel cartridge or 800 runs for 4-channel cartridge.
            5. The cartridge can be stored at 4~27°C and is valid for 6 months.
            S2 Cartridge (Standard Cartridge) BiOptic

            S1 High Resolution Cartridge Kit

            1. The analysis time is 2~5 minutes and the best resolution is 1~4bp if the sample size is less than 500bp.
            2. It provides high resolution result with multiple methods from low to high voltage (2~10kV) for user to choose from.
            3. It has a recommended analysis range up to around 5,000bp and a detection limit of about 0.1 ng/μl in low concentration.
            4. Each cartridge can analyze 200 runs for single-channel cartridge or 800 runs for 4-channel cartridge.
            5. The cartridge can be stored at 4~27°C and is valid for 6 months.
            S1 Cartridge BiOptic

            S3 Kilobase Cartridge Kit

            1. S3 cartridge is for large-sized DNA analysis.
            2. It has a recommended 5~165kb size range and is ideal for quality control of second and third generation sequencing.
            3. The system provides DNA Quality Number (DQN) for gDNA integrity reference.
            4. Each cartridge can analyze 200 runs for single-channel cartridge or 800 runs for 4-channel cartridge.
            5. The cartridge can be stored at 4~27°C and is valid for 6 months.
            S3 Cartridge BiOptic

            F3 Fast Cartridge Kit

            1. The analysis time is 90 seconds and can be applied to PCR product analysis.
            2. It has a recommended analysis range up to around 5,000bp for DNA.
            3. It runs on Qsep100 and Qsep400 only.
            4. Each cartridge can analyze 300 runs for single-channel cartridge or 1200 runs for 4-channel cartridge.
            5. The cartridge can be stored at 4~27°C and is valid for 4 months.
            F3 Cartridge BiOptic

            N1 High Sensitivity Cartridge Kit

            1. The sample concentration for analysis has a detection limit of about 5 pg/μl (or 1 pg/μl if dissolved in ddH2O) and the analysis time is about 3 minutes.
            2. It can be used for analysis of low concentration DNA fragment and quality control of cell-free DNA.
            3. It has a recommended analysis range up to around 5,000bp for DNA.
            4. Each cartridge can analyze 100 runs for single-channel cartridge or 400 runs for 4-channel cartridge.
            5. The cartridge can be stored at 4~27°C and is valid for 4 months.
            N1 Cartridge BiOptic

            N3 High Sensitivity Kilobase Cartridge Kit

            1. N3 cartridge is for low concentration large-sized DNA analysis.
            2. It has a recommended 5~165kb size range and is ideal for quality control of second and third generation sequencing.
            3. The system provides DNA Quality Number (DQN) for gDNA integrity reference.
            4. Each cartridge can analyze 200 runs for single-channel cartridge or 800 runs for 4-channel cartridge.
            5. The cartridge can be stored at 4~27°C and is valid for 4 months.
            N3 Cartridge BiOptic
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            BiOptic Consumables Portfolio

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              Qsep400 BiOptic

              Qsep400

              PRODUCTS

              Qsep400

              Qsep400

              4-channel Bio-Fragment Analyzer designed for medium and large-sized labs, offering higher throughput and faster analysis.

              Qsep400 features an integrated PC and touchscreen for user-friendly operation.

              Capable of analyzing DNA, RNA, or protein with a 4~96 sample capacity.

              Quantitative method provides comprehensive fragment size and concentration data in a single run.

              Qsep400 is a high-throughput automated Bio-Fragment Analyzer. It is the highest specification product of Qsep series and can analyze hundreds of samples in one day. It supports various types of applications, including DNA, RNA and protein fragment analyses and high-voltage fast analysis. Advantages of capillary electrophoresis are high resolution (1~4bp if less than 500bp), high sensitivity (5pg/μl) and significantly faster preparation and analysis time. Besides analyzing the fragment sizes and concentrations, it is also a tool for quality control, and is best for NGS facilities and research centers.

              Qsep400 is equipped with an integrated PC and touchscreen and can be directly controlled and analyzed. The system provides applications such as RNA quality control with RNA Quality Number (RQN) provided, auto-distribution of NGS QC and quality control of gDNA with DNA Quality Number (DQN) provided. Qsep400 is an independent and highly-efficient instrument.

              Qsep series can not only replace the complicated and time-consuming gel preparation and analysis procedure, but increase the accuracy of analysis, elevate efficiency and reproducibility, and reduce the human error and costs.

               

              Qsep400 BiOptic
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              BiOptic Instruments Portfolio

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                Qsep1-plus BiOptic

                Qsep1-Plus

                PRODUCTS

                Qsep1-Plus

                Qsep1-Plus

                Smallest/portable-sized capillary electrophoresis Bio-Fragment Analyzer for DNA, RNA, and protein.

                Qsep1-Plus is ideal for small laboratories with low throughput (1~15 samples) needs.

                The system supports Wi-Fi and cable connections, breaking the barriers of space.

                10+ types of cartridges can be easily exchanged between various applications.

                The provided quantitative method delivers fragment size and concentration information in one run.

                Qsep1-Plus has the highest specification product among all portable automated Bio-Fragment Analyzers. Advantages of capillary electrophoresis are high resolution (1~4bp if less than 500bp), high sensitivity (5pg/μl) and significantly faster preparation and analysis time. Besides analyzing fragment sizes and concentrations, it is also suitable for quality control of next-generation sequencing (NGS).

                Qsep1-Plus is equipped with completed hardware and software and has fully functional remote access via cable/Wi-Fi. The system provides various kinds of applications such as RNA quality control with RNA Quality Number (RQN) provided, auto-distribution of NGS QC and quality control of gDNA with DNA Quality Number (DQN) provided. Qsep1-Plus is a top choice for modern small or medium-sized laboratory.

                Qsep series can not only replace the complicated and time-consuming gel preparation and analysis procedure, but increase the accuracy of analysis, elevate efficiency and reproducibility, and reduce the human error and costs.

                Qsep1-plus BiOptic
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                BiOptic Instruments Portfolio

                Qsep100

                Qsep1

                Qsep400

                Qsep1+

                Qsep100 Advance

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                  Qsep100 BiOptic

                  Qsep100

                  PRODUCTS

                  Qsep100

                  Qsep100

                  Standard-sized capillary electrophoresis Bio-Fragment Analyzer for DNA, RNA, and protein.

                  Ideal for small to medium-sized labs with 1~96 sample capacity.

                  Easily exchangeable cartridges for versatile applications.

                  Provides quantitative data on fragment size and concentration in a single run.

                  Efficient Bio-Fragment Analysis with Qsep100

                  The Qsep100, a standard-sized automated Bio-Fragment Analyzer, represents the classic model in the Qsep series. Boasting a single-channel design, it can seamlessly process 1 to 96 samples, making it an ideal choice for small and medium-sized laboratories. This high sample flexibility extends to various applications, including DNA, RNA, and protein fragment analyses, as well as high-voltage fast analysis.

                  Versatility for Various Applications

                  The Qsep100 supports a range of applications, offering RNA quality control with the provision of RNA Quality Number (RQN), automated distribution of NGS QC, and quality control of genomic DNA (gDNA) with the availability of DNA Quality Number (DQN). Particularly, it stands out as a top choice for Next-Generation Sequencing Quality Control (NGS QC).

                  Streamlining Processes and Enhancing Accuracy

                  The Qsep series, including the Qsep100, eliminates the need for intricate and time-consuming gel preparation and analysis procedures. This not only increases the accuracy of analysis but also elevates overall efficiency and reproducibility while reducing human errors and costs. Invest in Qsep100 for a seamless, reliable, and efficient bio-fragment analysis experience.

                  Qsep100 BiOptic
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                  BiOptic Instruments Portfolio

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                    Qsep1 BiOptic

                    Qsep1

                    PRODUCTS

                    Qsep1

                    Qsep1

                    Smallest/portable-sized capillary electrophoresis Bio-Fragment Analyzer for DNA, RNA, and protein.

                    Ideal for small laboratories with low throughput needs (1~8 samples).

                    Supports Wi-Fi and cable connections, enhancing spatial flexibility.

                    Easy exchange of 10+ cartridges between various applications.

                    Quantitative method provides fragment size and concentration info in a single run.

                    Qsep1 is an automated Bio-Fragment Analyzer for DNA, RNA and protein fragments. Advantages of capillary electrophoresis are high resolution (1~4bp if less than 500bp), high sensitivity (5pg/μl) and significantly faster preparation and analysis time. Besides analyzing fragment sizes and concentrations, it is also suitable for quality control of next-generation sequencing (NGS).

                    Qsep1 is equipped with completed hardware and software and has fully functional remote access via cable/Wi-Fi. The system provides various kinds of applications such as RNA quality control with RNA Quality Number (RQN) provided, auto-distribution of NGS QC and quality control of gDNA with DNA Quality Number (DQN) provided. Qsep1 is a top choice for modern small laboratory.

                    Qsep series can not only replace the complicated and time-consuming gel preparation and analysis procedure, but increase the accuracy of analysis, elevate efficiency and reproducibility, and reduce the human error and costs.

                    Qsep1 BiOptic
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                    BiOptic Instruments Portfolio

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