Site Directed Mutagenesis

Mutants Synthesized. Mutagenesis Simplified.

Make Site-Directed Mutagenesis precise, simple, and affordable with Twist’s Mutagenesis by Synthesis. Traditional site-directed mutagenesis can be time consuming and imprecise. Site directed mutagenesis through synthesis eliminates these complexities, providing you with precisely engineered sequences tailored to your exact specifications. From protein engineering to functional genomics, incorporate precision synthesis of mutants into your workflow and focus on achieving your research goals

Why it matters to you:

Precision engineering – 

site-directed mutagenesis, custom DNA

Flexible design

protein engineering, functional genomics

Fast turnaround

Express Clonal Genes, rapid synthesis

Cost-effective

affordable variants, scalable synthesis

How to Qualify

Product: Clonal Genes
Number of mutation per genes: No Limit
Mutation type: any number of point mutation,
deletions, and/or insertions*
Pricing: Discounts on every variant
(Please kindly contact your Decode Sales Rep for enquiry)

How it Works

Terms and Conditions
* This promo is only available to customers in the Asia Pacific region (excluding China and Japan). Pricing is subjected to changes.
* To enjoy the special service of site directed mutagenesis, please quote your previous order number or approach Decode Science support.
* Each mutation is defined as any combination of bases change within a 10 codon spread over the entire gene.
* Average turnaround time for Express Clonal Genes is 4 -7 business days. This time will vary based on complexity and length of the sequence. Orders placed outside of the US will incur additional delivery turnaround time. Turnaround time for Clonal Genes is subject to change based on customizations and complexity. Additional specification: 50ng – 2 ug.

Watch Successful Implementations

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Screening Gene Libraries to Rapidly Identify Immune-recognised Virulence Genes.

Daina Elliott

Business Development Manager

As the authorized distributor of Twist Bioscience in Australia and New Zealand, Decode Science makes integrating Twist’s DNA synthesis solutions seamless. We connect your lab with high-throughput, high-fidelity Twist technology, enabling faster, more reliable genomic workflows—with local support and guidance every step of the way.
Twist Portfolio
Twist NGS

NGS

Raise confidence in variant detection with superior target enrichment solutions

Twist Oligo Pools

Oligo Pools

Precision, uniformity, and flexibility for results you can trust

Synthetic Controls

Synthetic RNA and DNA standards for assay development

Twist Libraries

Libraries

Identify more hits and streamline screening with Twist's precise Variant Libraries

Twist Genes

Genes

DNA Your Way: think bigger, expand your scope, and accelerate discovery in genes

Twist Antibody

Antibody

Robust solutions for Antibody Discovery and Development by Twist Bioscience

Comparison of Evercode™ WT v3 and Chromium™ GEM-X Single Cell 3’ Kit v4 in Mouse Brain Nuclei

Comparison of Evercode™ WT v3 and Chromium™ GEM-X Single Cell 3’ Kit v4 in Mouse Brain Nuclei

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    Comparison Highlights

    1. Evercode WT v3 delivers superior gene detection in head-to-head sensitivity tests.
    2. Cell type proportions remain consistently represented.
    3. Analysis of differential gene expression shows Evercode WT v3 identifies 2× more genes than competing methods.
    WT-vs-Gem-x-mouse-brain-tech-note-experimental-design-1536x546

    Study Overview
    Two embryonic mouse brains were sagittally dissected and flash-frozen by a third-party vendor.
    One half from each brain was processed by a 10x Genomics certified provider for nuclei isolation and library preparation, while the other halves were processed by Parse Biosciences using their own workflow.
    Sequencing was performed by a third-party, and data analysis was completed using each manufacturer’s respective pipeline.

    Dr. Ebru Boslem

    ANZ Market Manager - Research Genomics

    As the official distributor in Australia and New Zealand, Decode Science makes accessing genomics solutions straightforward. Our role is to connect your lab with advanced technologies, ensuring you get the right solution for your sequencing projects—delivered locally with support when you need it.

    Optimized CRISPR/Cas9 Gene Knockout PDF

    Accelerate knockout experiments with XDel’s next-generation CRISPR design.

    EditCo Bio’s XDel technology eliminates the need for guide RNA pre-screening, using a coordinated multi-gRNA design that delivers consistently high on-target editing across immortalized, primary, and iPSC lines. Validated through 768 edited samples and 4,816 NGS libraries, XDel achieves robust knockout efficiency while minimizing off-target effects—saving time and improving reproducibility across diverse cell types.

    Validated performance. Proven precision.
    With a standardized amplicon sequencing QC workflow and high-throughput automation, XDel enables scalable, high-confidence Cas9-mediated editing for both pooled and single-cell clone analysis. Download the full guide to explore the data, workflows, and results behind EditCo Bio’s high-efficiency gene knockout strategy.

    Optimized CRISPR/Cas9 Gene Knockout pdf EditCo Bio

    Unlock to Download Sheet

      Hamza Hassan

      Business Development Manager

      As the official distributor in Australia and New Zealand, Decode Science makes accessing genomics solutions straightforward. Our role is to connect your lab with advanced technologies, ensuring you get the right solution for your sequencing projects—delivered locally with support when you need it.

      Excel Sheet: STOmics Validated Tissue List

      STOmics Validated Tissue List

      Our STOmics validated tissue list provides researchers with a comprehensive reference of hundreds of tissue types successfully tested using Stereo-seq, the cutting-edge spatial transcriptomics technology. Each tissue entry includes detailed sample information, experimental parameters, and test results, allowing scientists to make informed decisions before starting their single-cell or spatial transcriptomics experiments. By consulting this list, you can ensure compatibility with your tissue samples and streamline your experimental design.

      The list not only highlights tissue types that have been validated but also provides insights into the experimental conditions that yielded the most reliable results. Researchers can leverage this information to optimize sample preparation, sequencing protocols, and data quality control measures. This reduces trial-and-error, saves valuable time and resources, and ensures reproducibility across studies. It is an essential tool for anyone planning to use Stereo-seq for spatial gene expression profiling.

      In addition, our STOmics validated tissue list supports better planning for large-scale studies and comparative analyses. By providing a centralized reference for tissue performance, it helps guide tissue selection, anticipate potential challenges, and maximize experimental success. Whether you are exploring new tissue types or scaling up existing workflows, this validated tissue list is your key resource for robust, high-quality spatial transcriptomics research.

      STOmics-Validated-Tissue-List

      Unlock to Download Sheet

        Notices:

        The STOmics validated tissue list was generated using standard tissue and sample types, all of which are frozen. Each tissue sample had an area of less than 1 cm² and was sectioned at a thickness of 10 μm. Most experiments were performed using the Stereo-seq Transcriptomics Kit V1.2, with a few using V1.1. Sequencing depth ranged from 1–3 G reads per sample, and data were processed using the Stereo-seq Analysis Workflow (SAW) versions V2.1.0–V5.1.3. Testing was conducted between 2020 and 2022.

        Please note that all test parameters and results are highly dependent on the tissue and sample type. This information should be used as a reference guide to help design and optimize your own experiments, rather than as definitive outcomes for all samples.

        Key parameters included in the list:

        1. MID (K): Bin200_Median_MID in thousands

        2. GENETYPE (K): Bin200_Median_Genetype in thousands

        Dr. Ebru Boslem

        ANZ Market Manager - Research Genomics

        As the official distributor in Australia and New Zealand, Decode Science makes accessing genomics solutions straightforward. Our role is to connect your lab with advanced technologies, ensuring you get the right solution for your sequencing projects—delivered locally with support when you need it.

        Data Set: Parse 10 Million Human PBMCs in a Single Experiment

        Scale Single-Cell Research Like Never Before

        Unlock with quick sign up!

          Key Takeaways

          1. Analyze 10 million cells across 1,152 samples in a single experiment

          2. Increase statistical power by profiling more cells per sample

          3. Capture detailed cellular responses to perturbations and drug treatments

          10 Million Human PBMCs in a Single Experiment

          Figure 1: Experimental Design Overview
          Approximately 10 million PBMCs from 12 healthy donors were treated with 90 different cytokines in a single GigaLab experiment, covering 1,092 experimental conditions.

          Cells were thawed, washed, and seeded at 1 million cells per well across 12 plates. After 24-hour cytokine treatment, cells were fixed, barcoded, and processed for whole transcriptome sequencing. Libraries were sequenced on the Ultima Genomics platform, achieving ~31,000 reads per cell, with 62.45% cell retention after barcoding.

          Results?

          After data processing with the Parse Analysis Pipeline v1.4.0, integration, and classification, 9,697,974 cells across 18 immune cell types were identified—including rare populations that are typically missed in smaller experiments. Each condition yielded a median of 7,400 cells, enabling high-resolution analysis of immune responses.

          Differential expression analysis identified how cytokines influenced gene activity across cell types. Many cytokines triggered strong transcriptional responses, with over 50 genes upregulated per treatment.

          Figure 2: Single-Cell UMAP Overview
          9,697,974 PBMCs from 12 donors were integrated with Harmony, clustered using Scanpy, and manually annotated, revealing 18 immune cell types present across all donors and experimental conditions.

          Figure 3: Cytokine-Induced Gene Changes
          A heatmap summarizes the averaged number of genes significantly upregulated (log fold change >0.3, p <0.001) for each cell type and cytokine, highlighting which immune cells respond most strongly to specific cytokine treatments.

          Example tutorial vignettes from Parse Biosciences and Fabian Theis’ lab at Helmoltz-Munich:

          Parse 10M PBMC Cytokines Clustering Tutorial
          Joey Pangallo, Efi Papalexi – Parse Biosciences, Seattle, WA
          Step-by-step example of analyzing 10 million PBMCs treated with cytokines using the Evercode workflow. Covers data loading, preprocessing, Leiden clustering, and generating UMAP plots with Scanpy.


          Parse 10M PBMC Cytokines Clustering Tutorial (Downsampled)
          Joey Pangallo, Efi Papalexi – Parse Biosciences, Seattle, WA
          Same workflow as above, starting with a downsampled dataset of 1 million cells. Ideal for quicker exploration or limited CPU memory setups.


          scCODA Parse 10M PBMC Cytokines
          Artur Szałata, Dominik Klein, Soeren Becker, Fabian Theis – Helmholtz-Munich
          Demonstrates analysis of cell proportion changes across 10 million PBMCs. Shows how using the full dataset improves statistical significance of perturbation effects. Based on scCODA, a Bayesian model for compositional single-cell data analysis (Nat Commun 12, 6876, 2021).


          Parse 10M PBMC Cytokines Dask Workflow
          Artur Szałata, Dominik Klein, Soeren Becker, Fabian Theis – Helmholtz-Munich
          Walks through preprocessing the 10M cell dataset using Dask. Loads data chunk-wise to reduce memory use and demonstrates highly variable gene selection for downstream analysis.


          Dataset License: CC BY-NC 4.0 (non-commercial use). Commercial licensing inquiries: support@parsebiosciences.com

          Dr. Ebru Boslem

          ANZ Market Manager - Research Genomics

          As the official distributor in Australia and New Zealand, Decode Science makes accessing genomics solutions straightforward. Our role is to connect your lab with advanced technologies, ensuring you get the right solution for your sequencing projects—delivered locally with support when you need it.

          DNBSEQ T7+

          MGI T7+ 2025
          T7+: Ultra-Fast, High-Throughput Sequencing Without Compromise

          T7+ is an integrated ultra-high-throughput sequencing platform built for labs that demand speed, accuracy, and scale. Leveraging MGI’s DNBSEQ™ Technology and SM2.0 biochemistry, it delivers over 14Tb of high-quality sequencing data in 24 hours, making large-scale genomics projects—from population studies to clinical pipelines—both feasible and efficient. Its 7-in-1 modular design automates the entire workflow, reducing hands-on time and minimizing potential errors.

          Beyond sheer performance, T7+ is engineered with clinical relevance in mind. Its capacity for up to 35,000 whole-genome sequences annually ensures that your lab can meet high-throughput demands without compromising turnaround times. This efficiency directly translates to faster research insights, improved diagnostic workflows, and smoother integration into daily lab operations, helping you focus on what matters most: accurate, actionable genomic data.

          >14 Tb/24h ultra-fast sequencing

          7-in-1 automation: prep to analysis

          QUAD-Flow Cells: PE150 & PE100 simultaneous

          Q40 >90% high-quality output

          Ergonomic & modular design

          Smart system with diagnostics & self-healing

          Omni-smart hub guides workflows

          Checkpoint resume for uninterrupted runs

          Learn more about how each feature works as you scroll.

          Watch How T7+ Works
          Why It Matters?

          Every hour matters when precision, speed, and reliability determine outcomes. T7+ addresses these challenges by combining ultra-high throughput, rapid turnaround, and intelligent automation, so you can focus on results rather than processes.

          Ultra-Fast Sequencing

          Ultra-Fast Sequencing:

          The proprietary TDI camera and high-density flow cells deliver over 14 Tb of high-quality data in 24 hours, supporting up to 35,000 whole-genome sequences per year. Large-scale projects can now be completed without bottlenecks.

          Seamless Automation

          Seamless Automation:

          The 7-in-1 workflow integrates DNB preparation, loading, sequencing, waste management, data analysis, and compression. This reduces hands-on time, minimizes errors, and produces ready-to-analyze FASTQ files with Q40 >90%.

          Chris Wicky

          Clinical Genomics Manager - ANZ & Country Manager - NZ

          Get a complete overview of T7+ performance, throughput, workflow automation, and configuration options. For guidance on integrating T7+ into your operations, Decode Science can provide personalized support and local assistance.
          Download T7 Plus Brochure

          Unlock with quick sign up!

            Omni Start Hub

            Smart & Intuitive Operation:

            Minimalist design, adjustable screen angles, and the Omni-smart hub guide operations with ease, making daily sequencing as simple as interacting with a smartphone.

            Data compression lossless

            Reliable Data Management:

            Built-in lossless data compression reduces storage and bandwidth needs by up to 5× without compromising accuracy. Intelligent checkpointing ensures sequencing resumes seamlessly after interruptions.

            Empower Multi-Omics

            Versatility for Multi-Omics:

            T7+ supports WGS, spatio-temporal omics, cell-omics, proteomics, epigenomics, transcriptomics, and more, making it adaptable to evolving research and operational needs.

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            FAQs
            What is a TDI Camera?

            A TDI (Time Delay and Integration) camera is a high-performance imaging system used in MGI’s T20×2 ultra-high throughput sequencer to capture fluorescence signals with exceptional sensitivity and speed. Unlike conventional cameras that take static images, a TDI camera continuously scans across the sequencing slide, synchronizing image acquisition with sample movement. This technique integrates multiple exposures of the same area over time, significantly boosting signal strength and reducing noise. In the T20*, the TDI line-scan cameras work alongside a liquid-immersion optical lens and a large field-of-view objective to capture more fluorescence data per unit time with higher resolution. The result is faster, more accurate base identification and greater sequencing throughput — a cornerstone technology enabling MGI’s record-breaking data generation efficiency.

            What is DNBSEQ Technology?

            DNBSEQ is MGI’s proprietary sequencing platform based on DNA Nanoball (DNB) technology. Instead of traditional bridge amplification used by other platforms, DNBSEQ amplifies DNA fragments through rolling circle replication, creating dense, uniform DNA nanoballs that are then arrayed on a patterned flow cell. This approach eliminates amplification errors, reduces duplication rates, and enhances signal precision. Combined with MGI’s two-color fluorescence detection and advanced imaging systems, DNBSEQ delivers high-throughput, low-cost, and highly accurate sequencing results. The platform supports a wide range of applications—from whole genome and single-cell sequencing to metagenomics and oncology research—while offering superior data consistency and scalability compared to conventional NGS systems.

            What is SM 2.0?

            Standard MPS 2.0 (SM 2.0) is MGI’s next-generation sequencing chemistry designed to significantly enhance the accuracy and performance of its DNBSEQ™ platforms. By refining enzyme systems, optimizing fluorescent dyes, and improving data interpretation algorithms, SM 2.0 delivers exceptional sequencing quality—achieving over 85% of bases at Q40, or 99.99% base-calling accuracy. These advancements reduce noise, improve signal clarity, and minimize bias from upstream preparation. As a result, researchers gain higher confidence in detecting low-frequency mutations, SNPs, and InDels across applications such as whole genome sequencing, single-cell studies, and microbiome analysis. In essence, SM 2.0 sets a new industry standard for precision, reliability, and data quality in high-throughput sequencing.

            What happens if there’s a power outage or system interruption during a run?

            T7+ features checkpoint resume technology and proactive fault detection, allowing sequencing to continue without data loss once power or system issues are resolved.

            How much hands-on time is required per sequencing run?

            The 7-in-1 integrated workflow minimizes manual intervention—preparation and monitoring are streamlined, so staff can focus on data analysis rather than instrument operation.

            Can T7+ handle varying sample volumes or project scales?

            Yes. The modular QUAD-Flow Cell system allows independent runs, supporting both small batches and large-scale sequencing without compromising speed or accuracy.

            How easy is it to integrate T7+ into an existing lab workflow?

            The platform is designed to fit seamlessly into existing operations, with smart guidance, automated data processing, and flexible output formats that simplify downstream analysis.

            Ready To Order?
            As the authorised distributor for MGI in Australia and New Zealand, Decode Science makes adopting the T7+ effortless. We connect your lab with MGI’s ultra-high-throughput sequencing technology, helping you implement T7+ for faster, more reliable genomic results—with local support and guidance whenever you need it.
            MGI Portfolio

            DNBSEQ-T1+

            Accelerate high-throughput genomic testing with DNBSEQ-T1+

            The DNBSEQ-T1+ is one of the fastest T-level benchtop sequencers available globally—built on MGI’s proven DNBSEQ™ technology for accuracy, scalability, and reliability. Designed for clinical and translational genomics labs, the T1+ supports dual flow cell operation, delivering up to 1.2 terabases (Tb) of sequencing data within 24 hours (600 Gb per flow cell).

            For laboratories managing time-sensitive or high-volume projects, this means faster turnaround, improved workflow efficiency, and reduced dependence on external bioinformatics infrastructure. The optional integrated bioinformatics module enables automated secondary analysis immediately after sequencing, helping clinicians and molecular pathologists move from raw data to interpretable results without delay.

            In practice, DNBSEQ-T1+ helps streamline comprehensive genomic profiling (CGP), oncology testing, and clinical research pipelines—supporting both diagnostic accuracy and operational consistency across runs.

            High-Speed, High-Throughput Sequencing

            Generate up to 1.2 Tb of data in a single run with dual flow cell operation.

            Choose from FCL, FCM, or FCS flow cells to match your throughput needs—from small clinical batches to large oncology cohorts.

            Maintain >93% Q30 and >90% Q40 base quality across read lengths up to PE150.

            Complete full runs in as little as 7–24 hours, supporting faster reporting and clinical turnaround.

            Versatile Applications Across Clinical Genomics

            Flexible read lengths (SE50–PE300) suit NIPT, RNA-Seq, oncology panels, WES, WGS, and methylation studies.

            Supports coverage depth from 1 Gb to 120 Gb per sample, enabling both targeted assays and whole-genome workflows.

            Ideal for translational and precision medicine—from pathogen detection to tumour profiling.

            Integrated DNB Make & Load Technology

            DNB M&L (Make & Load) module automates DNB preparation and loading directly within the sequencer.

            Delivers consistent, contamination-free results with minimal hands-on time.

            Each flow cell operates independently, supporting different read lengths or applications in parallel.

            Enables an end-to-end “Make–Sequence–Analyse” workflow that saves time and reduces error.

            Smart Configurations and Automated Analysis

            Available in two setups: DNBSEQ-T1+ RS (flexible throughput) and T1+ ARS (with built-in bioinformatics).

            The ARS configuration automatically triggers advanced data analysis post-run, streamlining bioinformatics pipelines.

            Simplifies data interpretation for clinicians and molecular pathologists, improving workflow efficiency and diagnostic accuracy.

            Chris Wicky

            Clinical Genomics Manager - ANZ & Country Manager - NZ

            Download the DNBSEQ-T1+ brochure for a complete overview of performance metrics, application data, and configuration options. For guidance on how this platform fits your lab’s workflow, Decode Science can walk you through integration and local support options.
            Watch How T1+ Works
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            FAQs
            How can the DNBSEQ-T1+ support my existing oncology or CGP workflows?

            The T1+ integrates seamlessly into oncology and comprehensive genomic profiling (CGP) pipelines, providing the depth and coverage needed for both solid tumour and liquid biopsy applications. With PE150 read lengths and up to 1.2 Tb per run, it supports multi-sample batching without compromising turnaround time.

            What data quality can I expect for clinical reporting?

            Across all flow cell types, >93% of bases exceed Q30 and >90% exceed Q40, ensuring high-confidence variant detection for SNVs, indels, CNVs, and fusions. This level of consistency reduces the need for re-runs and strengthens the reliability of reported results.

            How fast can I expect sequencing results for patient samples?

            Depending on the mode, runs complete within 7–24 hours, with automated secondary analysis available immediately post-run on the T1+ ARS configuration. This supports faster clinical reporting and improved patient turnaround.

            Does the DNBSEQ-T1+ simplify lab workflows or require extra setup?

            The DNB Make & Load module automates DNB preparation within the sequencer, reducing manual steps, contamination risk, and hands-on time. Most labs can run end-to-end sequencing with minimal intervention after library prep.

            Can I run different assays on the same instrument?

            Yes. Each flow cell operates independently, allowing different read lengths or applications—for example, running oncology panels alongside RNA-Seq or WES on the same instrument without downtime.

            Ready To Order?
            As the authorised distributor for MGI in Australia and New Zealand, Decode Science makes adopting the DNBSEQ-T1+ effortless. We bridge your lab with MGI’s high-throughput sequencing technology, helping you implement the T1+ for faster, more reliable genomic insights—supported locally whenever you need it.
            MGI Portfolio

            High Throughput Antibody Production

            PRODUCTS

            High Throughput Antibody Production

            Introducing CHO and HEK293 Antibody Production

            Twist Bioscience helps researchers speed up antibody discovery with Express Antibody Production using CHO and HEK293 expression systems. Our high-throughput antibody production platform can generate anywhere from dozens to thousands of antibodies, enabling efficient antibody screening for binding specificity and biophysical properties.

            By leveraging Twist’s end-to-end gene-to-protein workflow, you can eliminate common antibody production bottlenecks—saving valuable time and research costs. Starting with Twist Express Genes ensures faster production times and antibodies built entirely from your custom gene sequences.

            Key Features

            CHO Express Antibodies

            1. From 13 business days*
            2. 1 mL and 8 mL scales available
            3. Average Yields = 640 ug

            HEK293 Express Antibodies

            1. From 10 business days*
            2. 1 mL and 8 mL scales available
            3. Average = Yields 760 ug
            Why Twist for Antibody Production?

            Customization

            Design antibodies with optimal binding affinity, specificity, and reduced immunogenicity.

            Speed & Efficiency

            Rapid, sequence-perfect DNA synthesis accelerates your antibody development timeline.

            Scalable Production

            From small-scale studies to large-scale drug discovery, scale antibody production with ease.

            Cutting-Edge Technology

            Access the latest gene synthesis innovations without high costs.

            Expert Support

            Get 24/7 guidance from antibody design to submission.

            You design it. We build it.
            IgG Workflow - Antibody Production
            What Scientists Have to Say

            Wyatt McDonnell

            CEO & Founding Scientist • Infinnimune

            Using Twist’s solutions saves us hundreds of thousands of dollars annually in labor costs. The cost efficiency of Twist Express Antibodies allows us to test four times as many antibodies each year as we otherwise could.

            Dr. Ahuva Nissim

            Professor in Antibody and Therapeutic Engineering • Queen Mary University of London

            Working with Twist…was a great experience…[Twist’s] support was amazing. We have performed the first validation selections which looks promising…

            Pierre Martineau

            Deputy Director, Cancer Research Institute of Montpellier • Founder and Scientific Advisor, iMAb

            We have performed the first selections using the Fab and scFv libraries. No problem in both cases, we got clones and some look really promising.
            Ready To Order?
            Our team can help you in placing the order. Click below to get a quote and fast ordering.

            Know More About...

            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

              Arrayed gRNA Libraries

              PRODUCTS

              Arrayed gRNA Libraries

              Arrayed gRNA Libraries

              Smarter, Faster, and More Efficient CRISPR Screening

              Achieve unparalleled knockout efficiency with EditCo’s multi-guide CRISPR design. Our Arrayed CRISPR gRNA Libraries eliminate the inefficiencies of traditional loss-of-function screens, offering a reliable and ready-to-transfect solution. With up to three spatially coordinated sgRNAs per gene, our approach ensures higher knockout success, reduces false negatives, and eliminates the need for complex NGS data analysis. Designed for both human and mouse genes, our libraries provide fast delivery, robust quality control, and seamless Sanger sequencing analysis—so you can focus on results, not troubleshooting.

              Whole Genome CRISPR Libraries for Comprehensive Gene Editing

              EditCo’s Whole Human and Whole Mouse Genome Libraries provide unmatched gene coverage with our multi-guide design, ensuring high editing efficiency across 20,000+ gene targets. Designed for seamless transfection, these libraries reduce false negatives and eliminate time-consuming preparation, making large-scale CRISPR screening easier than ever.

              • – Comprehensive Coverage: Target the entire human or mouse genome with high knockout efficiency.
              • – Ready-to-Use Libraries: Pre-plated and transfection-ready, minimizing preparation time.
              • – Enhanced Stability: Chemically modified sgRNAs resist degradation and prevent immune responses.
              • – Flexible Formats: Available in 96- or 384-well plates with multi-guide sgRNAs for reliable gene disruption.
              Accelerate Target Discovery with Pathway Libraries

              EditCo’s 30+ Pathway Libraries, including druggable targets, GPCRs, kinases, and immuno-oncology genes, provide a powerful tool for target identification studies. Designed with our multi-guide CRISPR strategy, these libraries ensure high knockout efficiency and fewer false negatives. Select libraries ship in as little as one week, helping you start your screen faster.

              • – Diverse Pathway Coverage: Includes key gene sets for drug discovery and functional studies.
              • – Fast Shipping: Select libraries ready to ship within a week.
              • – High-Efficiency Knockouts: Multi-guide sgRNAs deliver precise, predictable gene disruption.
              • – Ready-to-Use Format: Available in 96- or 384-well plates with modified sgRNAs for stability.
              Available Gene Pathways
              Optimal Knockout Efficiency for High-Throughput Screening

               

              XDel technology delivers precise, high-efficiency knockouts by using a multi-guide RNA strategy that ensures consistent and reliable gene editing. Unlike traditional single-guide methods, XDel induces fragment deletions in early exons, maximizing on-target accuracy while minimizing variability and off-target effects.

              • Superior editing efficiency – Multi-guide design achieves higher and more consistent knockouts
              • Reduced off-target effects – XDel minimizes unintended edits compared to single-guide methods
              • Sustained knockout effects – Gene edits remain stable across multiple cell passages
              • High viability & protein depletion – Maintains cell health while ensuring effective functional knockouts

              Achieve robust genotype and phenotype screening with XDel’s optimized CRISPR knockout technology.

              XDel multiple gRNA creates fragment deletions

              Image: XDel multiple gRNA creates fragment deletions

              Image: XDel design includes up to 3 modified sgRNAs (grey bars) that target a single gene of interest

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

              Let’s Find You an Application That Helps Your Research

              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

                Gene Knockout Kits

                EditCo Gene Knockout Kits: Reliable and Efficient CRISPR Solutions

                EditCo’s Gene Knockout Kit offers a simplified, highly efficient solution for generating human and mouse protein-coding gene knockouts.

                Unlike traditional CRISPR methods, which rely on a single guide RNA (gRNA) to create random indels, EditCo’s multi-guide approach ensures consistent and precise gene disruption. This method generates fragment deletions at the targeted loci, providing a more reliable and predictable knockout, ultimately enhancing experimental success.

                With fast delivery times (kits arrive in just 5 days), users can avoid the trial and error of guide screening and proceed quickly with their experiments. The process is streamlined further with an easy online ordering portal, which includes the option to purchase controls, SpCas9 nuclease, and Transfection Optimization kits to complement your knockout experiment.

                This solution guarantees high knockout efficiency, making gene editing faster and more reliable than ever before.

                Why It Matters

                Maximise Gene Disruption

                XDel’s multi-guide CRISPR design consistently delivers higher on-target editing across multiple loci and cell types. By coordinating 2–3 sgRNAs per exon, researchers can achieve complete functional knockouts with minimal variability.

                Precision Editing with Minimal Risk

                Off-target edits are a major concern in gene editing. XDel’s cooperative guide approach allows for lower gRNA concentrations while maintaining efficiency, reducing unintended edits and improving experimental reliability.

                Persistent Protein Depletion, Straight to Assays

                Edited cell pools maintain stable protein loss for weeks, enabling direct use in downstream functional assays. This reduces validation cycles and accelerates your research timelines.

                Why Traditional Knockouts Fall Short

                Despite its power, CRISPR-Cas9 isn’t foolproof. Most conventional knockout strategies rely on a single guide RNA to induce a small insertion or deletion (indel) at the target site. In theory, this should disrupt the reading frame and deactivate the gene — but in practice, it rarely works that cleanly.

                Even minor indels can restore partial functionality or trigger alternative splicing, leaving residual protein activity that undermines downstream results. What should be a “complete knockout” often ends up a mosaic of mixed edits, forcing researchers to spend additional time validating, recloning, or repeating experiments.

                And it doesn’t stop there — when working with complex or sensitive cell models like iPSCs, low editing efficiency and variable expression recovery make reproducibility a constant battle. The result? Weeks lost, inconsistent phenotypes, and data that’s difficult to interpret or publish.

                Researchers need more than chance-based gene disruption.
                They need an approach that targets with precision, edits consistently across cell types, and produces true functional knockouts the first time.

                That’s exactly where XDel Technology steps in.

                Download Gene Knockout Kit Quick Start Guide

                Instant unlock with sign up!

                We respect your privacy and never spam with unrelated informaton.

                  XDel Technology – Coordinated, Multi-Guide Editing

                  Traditional CRISPR depends on a single cut — a gamble on where repair enzymes will introduce small, random indels. XDel takes a fundamentally smarter approach.

                  Instead of one guide, XDel uses up to three sgRNAs targeting sites within the same exon. These guides work together to generate coordinated fragment deletions, ensuring the targeted region is fully removed rather than partially disrupted. The result is a true functional knockout — not a mixture of partial edits.

                  This multi-guide design provides several key advantages:

                  • Higher knockout efficiency: Coordinated cuts increase the likelihood of complete loss of gene function across all alleles.

                  • Cleaner edit outcomes: Large, predictable deletions are easier to confirm with standard PCR or sequencing, reducing downstream validation time.

                  • Compatibility across cell types: Proven performance in immortalized, primary, and iPSC models — even those typically resistant to editing.

                  By shifting from random indels to engineered deletions, XDel dramatically improves experimental reproducibility and shortens the path from edit design to verified knockout.

                  Hamza Hassan

                  Business Development Manager- Research and Applied

                  Whether your work is in functional genomics, disease modeling, or drug discovery, XDel technology helps you achieve reproducible results faster and with less rework. Decode Science is the official Australian distributor of EditCo. So feel free to reach out to me if you have any questions.
                  Data-Proven Performance

                  XDel isn’t theory — it’s backed by real, quantitative data across multiple loci and cell types.

                  In comparative studies of seven endogenous genes across four different cell lines, XDel’s multi-guide approach consistently outperformed conventional single-guide designs in both knockout efficiency and edit consistency.

                  1. Higher and More Consistent On-Target Editing

                  Traditional single-guide methods introduce random indels that often yield partial or incomplete knockouts.
                  XDel solves this by deploying up to three predesigned sgRNAs targeting a single exon, working together to generate large fragment deletions.
                  Across seven endogenous loci in four cell lines, this approach achieved significantly higher and more consistent editing efficiencies — reducing the rework often required in CRISPR experiments.

                  On target Editing of XDel vs Single guide Knockout Cells
                  2. Stable Protein Depletion Across Time

                  Effective gene disruption means sustained loss of protein function, not just transient edits.
                  In K562 cells, XDel-mediated knockouts of four membrane proteins maintained stable protein depletion for up to 21 days post-editing — with >90% cell viability throughout.
                  These pools are immediately assay-ready, eliminating the need for additional validation or re-editing.

                  Click on image to view full size

                  3. Fewer Off-Target Edits, Greater Precision

                  A key concern with multi-guide systems is off-target activity — but XDel’s design delivers the opposite.
                  Rigorous NGS analysis across 63 off-target loci confirmed that XDel edits are more precise than single-guide approaches, showing markedly lower off-target frequencies across both immortalized and iPSC lines.

                  Off target Editing of XDel vs Single Guide Knockout cells
                  Off target editing across 46 off-target site in 4 immortalized or iPS cell lines
                  4. Confirmed Protein Knockout Across Multiple Genes

                  Western blot analyses for five independent target genes confirmed complete and consistent protein depletion at days 7, 14, and 21 post-transfection.
                  This demonstrates that XDel doesn’t just produce edits — it reliably eliminates functional protein expression across diverse gene targets.

                  Protein Depletion - Gene Knockout Cells
                  5. High Editing Efficiency at Lower gRNA Concentrations

                  The cooperative behavior of XDel’s multi-guide system enables lower total gRNA usage while maintaining exceptional on-target editing rates.
                  Even when RNP concentrations were reduced to 0.25×, editing remained high with minimal off-target impact — translating to more cost-efficient and cleaner edits.

                  High Editing Efficiency at Lower gRNA Concentrations
                  Applications Across Research Areas

                  Functional Genomics

                  Disease Modeling

                  Drug Discovery and Target Validation

                  CRISPR Screening and High-Throughput Studies

                  Talk to Our Specialist
                   

                  Decode Science is the official distributor of EditCo in Australia and New Zealand, helping researchers access XDel Knockout Technology with local expertise and technical support. Our team works alongside you to identify the right solutions for your workflow — from targeted knockouts to large-scale CRISPR screens — backed by EditCo’s proven data and Decode’s commitment to reproducibility.

                  For more information or project-specific guidance, reach out to Hamza Hassan, our business development manager, to discuss how XDel can accelerate your next experiment.

                  CRISPR Reagents Portfolio