MGISP-Smart 8

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MGI Smart 8

The MGISP-Smart 8 features a self-contained 8-channel pipette, meticulously crafted to address a wide spectrum of pipetting requirements spanning from 1 μL to 1000 μL. This versatile system is compatible with microplates, reservoirs, and tubes, reducing the likelihood of human errors while enhancing efficiency with its integrated PCR machine, shaker, and temperature control capabilities. With its resilient adaptability, the MGISP-Smart 8 stands as an exemplary solution for precision and convenience in laboratory environments.

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Your Independent 8-channel Pipetting Robot

Flexible Pipetting

Its pipetting based on air displacement , which ensures stability, accuracy and avoids cross-contamination.

Easy and Efficient

Graphical interface with intelligent guidelines and contains 9 functional instructions and 35 modular commands.

Modular design

Combine, replace or rearrange functional modules & carriers & adapters, flexibly serving different application scenarios.

Chris Wicky

Clinical Genomics Manager - ANZ & Country Manager - NZ

As the official distributor of MGI in Australia and New Zealand, Decode Science is providing local access to Smart 8 solutions with region-based technical and application support. Simply talk to me and we can discuss your research needs.

Get In Touch Today
How to Choose

Choose your workstation based on how much of your workflow you want automated. From flexible liquid handling and reaction setup to fully automated nucleic acid extraction and high-throughput library preparation, each configuration is designed to match a specific level of complexity and scale. Download the brochure to see detailed workflows, modules, and specifications.

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    System Parameters

    Fully automated quantification

    • When integrated with a microplate reader, it enables fully automated quantification and normalization/pooling of PCR libraries, DNB samples, and extracted products, enhancing the automation of the entire library workflow and boosting laboratory efficiency.

    Operating Environment Requirements

    • Temperature: 15℃~35℃
    • Humidity: 20% RH~80% RH, non-condensing
    • Atmospheric Pressure: 80 kPa~106 kPa

    Intelligent & Informed

    • Sensing and barcode scanning functions reduce human error, ensure experimental stability, and automatically record critical experiment information.

    Power, Dimensions & Net Weight

    • Voltage: 200 V~240 V, 50/60 Hz
    • Rated Power: 1500 VA (not including modules on the operation deck and optional modules)
    • Dimensions (W×H×D): 1410 mm × 799 mm × 970 mm (without HEPA module)
    • Weight: approximately 220 kg (485 lb, without carriers)

    Operating Environment Requirements

    • Temperature: 15℃~35℃
    • Humidity: 20% RH~80% RH, non-condensing
    • Atmospheric Pressure: 80 kPa~106 kPa
    Product Specifications
    Pipette TypeIndependent 8-channel pipette
    Pipette Range1 μL – 1000 μL
    Robot Arm Positioning Accuracy±0.1 mm
    UV LampRadiation dose > 100,000 μW·s/cm²
    MGI Portfolio

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      RNA Sequencing

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      PRODUCTS

      RNA Sequencing

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      RNA Sequencing

      Twist’s RNA sequencing workflows offer a complete NGS solution that produces uniform libraries for RNA sequencing.

      Twist offers targeted and whole transcriptome workflows that reduce time at the bench and integrate with our current set of NGS reagents, including our target enrichment kits. Each workflow delivers high quality libraries ready for sequencing from a wide range of inputs and sample types, including translation research samples.

      Get a Quote
      RNA Library Prep

      Twist offers two comprehensive RNA sequencing workflows: Targeted RNA Sequencing and Whole Transcriptome Sequencing. The Targeted RNA Sequencing workflow involves creating custom panels to focus on specific RNA transcripts, utilizing streamlined library preparation kits, unique dual indices, molecular identifiers, optimized target enrichment, and a proprietary exon-aware panel design algorithm. This allows for sensitive and efficient sequencing, even with low-quality RNA from FFPE samples.

       

      On the other hand, the Whole Transcriptome Sequencing workflow measures expression levels of various RNA species, including mRNA and lncRNA. It involves preparing libraries from total RNA extracted from both fresh and FFPE samples using Twist RNA Library Prep and Twist rRNA & Globin Depletion kit. This workflow enables RNA Library Preparation in less than 5 hours, providing a comprehensive view of the entire transcriptome. Two charts accompany the descriptions, detailing the targeted and whole transcriptome sequencing workflows.

      RNA Sequencing
      Twist Targeted RNA Sequencing Workflow
      Twist Whole Transcriptome Sequencing Workflow
      More Targets, Fewer Reads
      RNA Exome

      The collaboration of Twist RNA Exome, Twist RNA Library Prep, and Twist Target Enrichment forms a reliable toolkit for transcriptome sequencing, accommodating RNA from diverse sources, including FFPE samples. Notably, the RNA Exome enhances signal strength while requiring fewer sequencing reads, enabling the detection of low-expressing targets crucial for accurate transcriptional profiling. Its exon-aware design approach allows the identification of isoforms and junctions often overlooked in conventional methods, delivering precise and uniform sequencing reads tailored for analyzing protein-coding sequences within the human transcriptome.

       

      Designed exclusively for the human transcriptome, the RNA Exome targets 35.8 Mb bases, 19,708 genes, and 63,215 isoforms using sequences from Gencode and RefSeq. With over a 1.8-fold enrichment compared to whole transcriptome sequencing, it features a target enrichment approach built for RNA, incorporating an exon-aware probe design for protein coding regions, fusions, and isoforms. This design not only ensures precision but also reduces reads per sample, facilitating efficient analysis of multiple samples. The RNA Exome is versatile, compatible with FFPE samples and low RNA input. In practical tests, it demonstrates the capability to detect more targets with fewer reads across a range of RNA inputs, including FFPE and universal human reference RNA, using libraries prepared with the Twist RNA Library Prep.

      RNA Fusion

      The Twist Alliance CeGaT RNA Fusion Panel Kit emerges as a crucial tool in the precise detection of gene fusions, particularly impactful oncogenic driver mutations in various cancer types. Rapid and accurate detection holds significant clinical implications, guiding treatment decisions effectively. This RNA-based enrichment panel stands out by offering an enhanced targeted and sensitive approach, surpassing traditional methods.

       

      Curated in collaboration with CeGaT, a renowned genetic diagnostic and sequencing company in Europe, this panel encompasses 160 fusion genes associated with approximately 30 cancer types. Uniquely, it is designed not only for known gene fusions but also to unveil novel ones. The panel’s efficiency is amplified when used in conjunction with the Twist RNA Library Prep Kit, ensuring an end-to-end workflow with exceptional performance.

       

      With an optimized design featuring 7394 probes and a breakpoint design for 66 genes, the panel excels in covering a diverse array of cancer types. The incorporation of Twist core enrichment technology further maximizes capture efficiency, instilling confidence in RNA gene fusion detection. This panel is particularly well-suited for screening oncology samples, providing critical insights for treatment decisions or uncovering novel fusions for tumor classifications.

       

      *Note: The Twist Alliance CeGaT RNA Fusion Panel – 3 MB holds ISO-13485 certification, reinforcing its reliability in clinical applications.

      Ready To Order?
      Our team can help you in placing the order. Click below to get a quote and fast ordering.
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      NGS Portfolio

      Custom Panels

      Viral Panels

      Methylation Detection

      RNA Sequencing

      MRD Sequencing

      Long Read Sequencing

      Library Preparation

      Other Panels

      Have a question?

      Get a call from your local Decode Science representative to help you find the best fit genomics products for you.

        Or give us a call at:

        1300 581 991

        MRD Sequencing

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        PRODUCTS

        MRD Sequencing

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        MRD Sequencing

        Minimal Residual Disease (MRD), characterized by a small number of lingering malignant cells post-treatment, poses a recurrence risk often undetectable by standard surveillance methods. Twist Bioscience’s MRD Rapid 500 Panel addresses this challenge by utilizing circulating tumor DNA for early detection. Leveraging Twist’s silicon-based DNA synthesis platform, this scalable solution offers rapid turnaround time (as few as 6 business days) with personalized variant profiles from whole-genome or whole-exome sequencing. The MRD panels, featuring 50 to 500 probes, provide comprehensive genomic insights, compatible with Twist’s NGS library preparation and hybrid capture workflow. This facilitates early intervention and enhances personalized medicine approaches in cancer recurrence monitoring.

        Get a Quote
        Benefits

        Unmatched Scalability and Speed:
        Benefit from unparalleled scalability and efficiency as you capture variants of interest with panels ranging from 50 to 500 probes. Streamline your workflow by ordering up to 150 panels at a time, and experience the rapid shipment of panels within an impressive 6 business days.

        Customized Panel Designs:
        Tailor your panel designs to meet your specific needs using a variant target coordinate BED file. Improve capture performance by strategically filtering probe sequences over repetitive regions, leading to enhanced efficiency and significant cost savings on overall sequencing expenses.

        Panel Information:
        Leverage the advantages of a single plex for 12 tests, ensuring the detection of SNVs and small indels with high precision. Implement quality control through qPCR, and rest assured with ISO-13485 certification, signifying a commitment to reliability. Conveniently receive panels in Matrix Tubes, and benefit from designs supported against hg19 and hg38 reference genomes.

        Lab Workflow:
        Integrate seamlessly into your lab workflow with compatibility with Twist library preparation and hybridization workflows. Follow the recommended hybridization protocol, MRD Standard Hyb 2.0, ensuring not only efficiency but also a streamlined and harmonious laboratory process.

        MRD Rapid 500 Panel Design
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        Our team can help you in placing the order. Click below to get a quote and fast ordering.
        Get a Quote
        NGS Portfolio

        Custom Panels

        Viral Panels

        Methylation Detection

        RNA Sequencing

        MRD Sequencing

        Long Read Sequencing

        Library Preparation

        Other Panels

        Have a question?

        Get a call from your local Decode Science representative to help you find the best fit genomics products for you.

          Or give us a call at:

          1300 581 991

          Long Read Sequencing

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          PRODUCTS

          Long Read Sequencing

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          Long Read Sequencing

          Combine the precision of Twist target enrichment with the power of long read sequencing to efficiently explore crucial genomic regions at scale. Twist Alliance panels, both pre-designed and customizable, empower researchers to capture target regions in a cost-effective and high-throughput manner, ensuring exceptional performance.

          Exceptional Performance: Elevate your sequencing endeavors with panels specifically crafted for long read sequencing. Probes are optimized for high uniformity and sequencing efficiency, ensuring balanced coverage even across challenging-to-sequence or difficult-to-map genomic regions.

          Long Read Sequencing at Scale: Efficiently scale up your sequencing projects with a protocol optimized for long fragment enrichment. This approach allows you to pack more samples into a single sequencing run, making it possible to study targeted regions across large cohorts.

          Accurate Variant Calling with Targeted HiFi Sequencing from PacBio: Leverage the accuracy of targeted HiFi Sequencing from PacBio for precise variant calling of SNPs, SVs, and indels. Benefit from unambiguous haplotype resolution and long-range phasing, ensuring reliable results. This approach is compatible with Sequel IIe and Revio Systems, providing versatility in sequencing platforms.

          Get a Quote

          Twist Alliance Dark Genes Panel
          Enables sequencing of genes that are difficult or impossible to fully sequence with short read technology.

          1. Targets 389 genes (20 Mb)
          2. Key targets include GBA, SMN1/2

          Twist Alliance Long-Read PGx Panel
          Focus on important genes in pharmacogenomics that are critical to drug metabolism and patient therapeutic response.

          1. Targets 49 genes (2 Mb)
          2. Key targets include CYP2D6, HLA-A, HLA-B
          Twist Alliance Dark Genes Panel
          Twist Alliance Long-Read PGx Panel
          Ready To Order?
          Our team can help you in placing the order. Click below to get a quote and fast ordering.
          Get a Quote
          NGS Portfolio

          Custom Panels

          Viral Panels

          Methylation Detection

          RNA Sequencing

          MRD Sequencing

          Long Read Sequencing

          Library Preparation

          Other Panels

          Have a question?

          Get a call from your local Decode Science representative to help you find the best fit genomics products for you.

            Or give us a call at:

            1300 581 991

            Library Preparation

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            PRODUCTS

            Library Preparation

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            Library Preparation

            Twist Library Preparation Kits offer a streamlined process for constructing high-quality DNA libraries in next-generation sequencing (NGS) applications. Tailored for whole genome sequencing and targeted enrichment, these kits simplify library preparation by combining multiple steps into a single reaction, enhancing efficiency and ensuring consistent results.

            Two configurations are available to cater to different needs: Mechanical Fragmentation, designed for mechanically sheared gDNA, and Enzymatic Fragmentation, ideal for automated, high-throughput library preparation. Both configurations minimize artifacts, accommodate various DNA input types, and optimize sequencing of low-quality samples, with the Enzymatic Fragmentation offering tunable, reproducible fragment sizes while minimizing sequence bias and maximizing coverage depth.

            Get a Quote

            Library Preparation Workflow

            The Twist Library Preparation Kits provide a comprehensive solution for the entire library preparation workflow, encompassing crucial steps such as end repair, dA-tailing, adapter ligation, and library amplification. Both kits offer versatility in adapter choices, allowing the use of either full-length or universal adapters based on specific application requirements.

            For the Enzymatic Fragmentation Kit, additional functionality includes the incorporation of enzymes for the fragmentation of genomic DNA (gDNA) samples. This feature enhances the kit’s capability for high-throughput library preparation.

            The accompanying chart illustrates a robust library construction process by utilizing Twist Universal Adapters for insert ligation and UDI primer PCR amplification. This approach ensures a streamlined and efficient workflow, producing libraries suitable for a diverse range of applications.

            Ready To Order?
            Our team can help you in placing the order. Click below to get a quote and fast ordering.
            Get a Quote
            NGS Portfolio

            Custom Panels

            Viral Panels

            Methylation Detection

            RNA Sequencing

            MRD Sequencing

            Long Read Sequencing

            Library Preparation

            Other Panels

            Have a question?

            Get a call from your local Decode Science representative to help you find the best fit genomics products for you.

              Or give us a call at:

              1300 581 991

              purePlex™ DNA Library Prep Kit

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              PRODUCTS

              purePlex™ DNA Library Prep Kit

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              purePlex™ DNA Library Prep Kit

              A benefit to purePlex is that, because of its simplicity, users can quickly and seamlessly incorporate the kit with existing methods for high-throughput pipetting.

              Speed, Performance, and Auto-Normalization with Unique Dual Indexes

              1. 2.5-hour workflow for 96 samples, 45 min. hands-on time
              2. Auto-normalization of read counts and insert size over 10-fold input range
              3. Unique dual indices included
              Get a Quote
              purePlex™ DNA Library Prep Kit seqWell

              Key Features

              1. Fast, flexible workflow with no requirement for full plate processing
              2. Auto-normalization reduces QC burden, improves data consistency
              3. Early pooling for easier sample handling
              4. Reduced GC bias compared to other transposase-based methods
              5. Significant cost and plastics savings

              purePlex™ DNA Library Prep Kit Workflow seqWell

              purePlex™ DNA Library Prep Kit Workflow seqWell
              Ready To Order?
              Our team can help you in placing the order. Click below to get a quote and fast ordering.
              Get a Quote
              SeqWell Portfolio

              plexWell™ LP 384

              plexWell™ 96

              plexWell™ 384

              ExpressPlex

              Tagify

              purePlex

              Have a question?

              Get a call from your local Decode Science representative to help you find the best fit genomics products for you.

                Or give us a call at:

                1300 581 991

                ExpressPlex™ Library Prep Kit

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                PRODUCTS

                ExpressPlex™ Library Prep Kit

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                ExpressPlex™ Library Prep Kit

                Designed for quick turnaround of plasmid, amplicon, or synthetic construct sequencing, ExpressPlex* is the fastest high-throughput library preparation kit available (based on total time to prepare 96 – 384 samples).

                1. 90-min workflow with 30-min or less hands-on
                2. Fragmentation, barcoding, and amplification in 1 step
                3. No primers/barcodes to buy
                4. Virtually cross-talk free
                5. Up to 6,144 samples prepped and sequenced in 24 hours
                6. NEW: 384-well ultra-high throughput version available
                *Patents Pending
                Get a Quote
                ExpressPlex™ Library Prep Kit SeqWell

                Benefits of using ExpressPlex

                ExpressPlex allows you to spend your time on data and results, not pipetting.  There are solutions for low-, medium-, and high-throughput labs.  For ultra-high throughput users, we now offer 384-well versions that will enable you to multiplex up to 6,144 samples in a single run. 

                1. Go from extracted samples to libraries on the sequencer in < 1/2 a day
                2. Sequence more samples for less
                3. Easily automate your protocol
                4. Train any lab tech, minimize chance for error
                5. Choice of 96 or 384-well versions to fit your workflow
                6. Reduce labor while increasing efficiency
                7. Decrease chance for errors via minimal handling steps
                8. Everything included: no complex supply chain management of barcodes and primers
                ExpressPlex 2.0 seqWell

                ExpressPlex 96-Well Workflow

                ExpressPlex-Workflow-1024x682

                ExpressPlex 384-Well Workflow

                ExpressPlex-384-WFG-1-1024x918
                Ready To Order?
                Our team can help you in placing the order. Click below to get a quote and fast ordering.
                Get a Quote
                SeqWell Portfolio

                purePlex

                plexWell™ LP 384

                plexWell™ 96

                plexWell™ 384

                ExpressPlex

                Tagify

                Have a question?

                Get a call from your local Decode Science representative to help you find the best fit genomics products for you.

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                  1300 581 991

                  Tagify

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                  Are You Confident in Your Gene Editing Results?

                  If you’re not validating every edit with high-quality sequence analysis, you’re guessing — and guessing has no place in CRISPR, TALEN, or ZFN workflows.

                  Accurate gene editing QC is essential for verifying edits, detecting off-target events, and protecting downstream research or therapeutic development. Robust sequencing isn’t optional — it’s your safety net.

                  Scalable, High-Fidelity QC for Every Gene Editing Workflow

                  Tagify adapter-loaded transposases

                  Rapid, simplified library prep for on-target and off-target QC, enabling precise detection of editing outcomes at scale.

                  ExpressPlex® 2.0 library preparation

                  Ultra-efficient multiplexed prep for high-throughput construct screening, ideal for CRISPR guide validation, pooled editing campaigns, and engineered cell line development.

                  On-Target & Off-Target Gene Editing QC

                  Tagify® Adapter-Loaded Transposase for High-Confidence Tagmentation

                  Accurate characterization of on-target and off-target editing events is non-negotiable. Insertions, deletions, inversions, translocations — every outcome needs to be detected and verified. Yet standardized QC methods for gene editing are still early-stage, especially for off-target analysis. Most teams end up navigating inconsistent protocols, variable reagent quality, and limited scalability.

                  Reliable, QC-Verified Reagents for Tagmentation-Based Gene Editing Assays

                  Tagify reagents remove the uncertainty. Each lot is fully QC-checked and delivered as ready-to-use or custom-loaded hyperactive Tn5 or TnX, seqWell’s next-generation transposase engineered for dependable performance.

                  With Tagify, you get:

                  1. Consistent tagmentation performance
                  2. Scalable workflows for high-throughput QC
                  3. Reagents optimized for sensitive off-target detection

                  Broad Compatibility with Leading Gene Editing QC Methods

                  Tagify reagents integrate seamlessly with widely used transposase-based assays including:

                  1. GUIDE-seq²
                  2. UDiTaS
                  3. CHANGE-seq
                  4. RGEN
                  5. TTIS-seq
                  6. and additional emerging QC workflows

                  *Some transposase-based methods require appropriate licensing.

                  Useful Webinars

                  Assessing CRISPR On-Target Editing and Structural Changes

                  High-throughput Construct Screening

                  Chris Wicky

                  Clinical Genomics Manager - ANZ
                  & Country Manager - NZ

                  If you’re looking to integrate these QC solutions into your pipeline, Decode Science can provide hands-on guidance and local expertise.
                  TALK TO ME DIRECTLY
                  Happy Customer Feedback
                  "We’ve been asking for this. What’s great about Tagify is that it allows you to look at a specific place in the gene, and adapter concentration is taken care of. This system is really important because it provides us this opportunity to assess the consequences of gene editing in a semi-unbiased way. It shortens our process, makes it much more controlled, and lessens the amount of reagents we need to use.”
                  – Athea Vichas, Ph.D., Senior Principal Scientist of Gene Editing Analytical Development, Bristol Myers Squibb
                  “ExpressPlex is literally faster than Sanger. This changes everything for us. Basically, taking a two-day process to one day dramatically shortens time to data.”
                  – Henry Chan, Ph.D., Synthetic Biology Lead, Octant Bio
                  SeqWell Portfolio

                  purePlex

                  plexWell™ LP 384

                  plexWell™ 96

                  plexWell™ 384

                  ExpressPlex

                  Tagify

                  plexWell LP 384

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                  PRODUCTS

                  plexWell LP 384

                  Get a Quote

                  The plexWell™ LP 384 kit is engineered for low-pass whole genome library preparation and sequencing, utilizing the enhanced plexWell workflow. The kit includes major reagents essential for library preparation, featuring Magwise™ paramagnetic beads (DNA polymerase not included). This kit allows efficient library preparation for more than one 96-well plate of samples and normalizes input DNA over a wide range of 5-25 ng.

                  plexWell™ LP 384 (Low-Pass Whole Genome) Highlights:

                  • NGS multiplexed library generation kit designed for Illumina® platforms.
                  • Features assay-ready 96-well fully-skirted low-profile PCR plates in sets of 4 (4 x 96).
                  • Provides 2,304 (96 x 24) unique barcode combinations.
                  • Includes 6 sets of 4 pool barcodes (PB Set A, B, C, D, E, or F).

                  Recommended Application: Ideal for low-depth whole genome/GBS (Genotyping by Sequencing) coupled with imputation and analysis software for comprehensive genomic studies.

                  Get a Quote

                  plexWell™ Library Prep Workflow:

                  plexWell™ Library Prep Chemistry:

                  plexWell96
                  Ready To Order?
                  Our team can help you in placing the order. Click below to get a quote and fast ordering.
                  Get a Quote
                  SeqWell Portfolio

                  purePlex

                  plexWell™ LP 384

                  plexWell™ 96

                  plexWell™ 384

                  ExpressPlex

                  Tagify

                  Have a question?

                  Get a call from your local Decode Science representative to help you find the best fit genomics products for you.

                    Or give us a call at:

                    1300 581 991

                    plexWell

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                    PRODUCTS

                    plexWell

                    Get a Quote
                    plexWell 96

                    The plexWell™ 96 (PW096) kit streamlines NGS multiplexed library generation for Illumina® platforms, housed in an assay-ready 96-well fully-skirted low-profile PCR plate. The kit includes major reagents, featuring Magwise™ paramagnetic beads (DNA polymerase not included), facilitating efficient library preparation for one 96-well plate inputs. Notably, it offers normalization of input DNA over a broad range of 3-30 ng, with a cost-saving volume-based pricing structure that can reduce total lab costs by 30-50%.

                    Key Features:

                    • Comprehensive kit with Magwise™ beads.
                    • Efficient library prep for one 96-well plate.
                    • Normalization of input DNA (3-30 ng).
                    • Volume-based pricing for cost savings.

                    Recommended Applications: Ideal for large-scale full-length viral surveillance, Synthetic Construct Sequencing (Amplicons, Plasmids, BACs, etc.), microbiome screening, microbial whole-genome sequencing, scRNA-seq (single-cell RNA sequencing), and low-depth whole-genome/GBS (genotyping by sequencing).

                    Get a Quote
                    plexwell-lps-384-featured-1
                    plexWell 384

                    The plexWell™ 384 (PW384) kit is a comprehensive solution for NGS multiplexed library generation on Illumina® platforms. Each kit includes major reagents, featuring Magwise™ paramagnetic beads (DNA polymerase not included), essential for efficient library preparation for more than one 96-well plate of samples. This kit offers normalization of input DNA across a wide range of 3-30 ng, with a cost-saving volume-based pricing structure, reducing total lab costs by 30-50%.

                    Key Features:

                    • Comprehensive kit with Magwise™ paramagnetic beads.
                    • Efficient library prep for more than one 96-well plate.
                    • Normalization of input DNA (3-30 ng).
                    • Cost-saving volume-based pricing.

                    Recommended Applications:

                    • Large-scale full-length viral surveillance.
                    • Synthetic Construct Sequencing (Amplicons, Plasmids, BACs, etc.).
                    • Microbiome screening.
                    • Microbial whole-genome sequencing.
                    • scRNA-seq (single-cell RNA sequencing).
                    • Low-depth whole-genome/GBS (genotyping by sequencing).
                    Get a Quote
                    plexwell-lps-384-featured-1

                    plexWell™ Library Prep Workflow:

                     

                    plexWell™ Library Prep Chemistry:

                    plexWell96
                    Ready To Order?
                    Our team can help you in placing the order. Click below to get a quote and fast ordering.
                    Get a Quote
                    SeqWell Portfolio

                    purePlex

                    plexWell™ LP 384

                    plexWell™ 96

                    plexWell™ 384

                    ExpressPlex

                    Tagify

                    Have a question?

                    Get a call from your local Decode Science representative to help you find the best fit genomics products for you.

                      Or give us a call at:

                      1300 581 991