Site Directed Mutagenesis

November 17, 2025/in Partners, Synbio Genes, Twist/by Harshita Sharma

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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Designing Enzymes for the Infinite Recycling and Upcycling of Plastic

WEBINAR

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

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

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

November 13, 2025/in Parse/by Harshita Sharma

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

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Comparison Highlights

Evercode WT v3 delivers superior gene detection in head-to-head sensitivity tests.
Cell type proportions remain consistently represented.
Analysis of differential gene expression shows Evercode WT v3 identifies 2× more genes than competing methods.

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.

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

November 13, 2025/in EditCo, Partners/by Harshita Sharma

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.

Unlock to Download Sheet

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

October 30, 2025/in STOmics/by Harshita Sharma

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.

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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:

MID (K): Bin200_Median_MID in thousands
GENETYPE (K): Bin200_Median_Genetype in thousands

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

October 30, 2025/in Parse/by Harshita Sharma

Scale Single-Cell Research Like Never Before

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Key Takeaways

Analyze 10 million cells across 1,152 samples in a single experiment
Increase statistical power by profiling more cells per sample
Capture detailed cellular responses to perturbations and drug treatments

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

QUICK DOWNLOAD FILES

10M PBMC 12donor 90cytokines h5ad (212 GB)

Parse 10M PBMC cytokines clustering tutorial

Parse 10M PBMC cytokines clustering tutorial on downsampled data

scCODA Parse 10M PBMC cytokines

Parse 10M PBMC cytokines Dask workflow

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+

October 22, 2025/in MGI, Partners, Sequencing Platforms/by Harshita Sharma

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.

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.

DNBSEQ T7+

DNBSEQ-T1+

DNBSEQ-E25

DNBSEQ-G400

DNBSEQ-T7

DNBSEQ-G99

Twist Oncology – DNA CGP Panel

October 9, 2025/in Oncology/by Harshita Sharma

PRODUCTS

Comprehensive Genomic Profiling for Oncology Research

The new Twist Oncology - DNA CGP panel offers 562-gene coverage for complete tumour profiling

Comprehensive Genomic Profiling (CGP) uses next-generation sequencing (NGS) to evaluate multiple clinically relevant biomarkers within a solid tumor. It provides detailed genomic resolution, enabling the detection of single nucleotide variants (SNVs), insertions and deletions (indels), copy number variations (CNVs), select gene fusions, and key cancer genomic signatures such as tumor mutational burden (TMB) and microsatellite instability (MSI).

By consolidating this information into a single assay, CGP offers a complete view of a tumor’s molecular profile, reducing the need for multiple tumor-specific panels or separate testing methods.

Why CGP Matters

Unified Testing Platform

Combines samples from all tumor types into a single test platform, enabling efficient batching and streamlined workflow.

Actionable Insights

Focuses on clinically and research-relevant information, supporting treatment decisions and drug development strategies.

Cost-Effective Efficiency

More efficient and economical than whole-exome sequencing (WES) for oncology, lowering resource use while maintaining comprehensive genomic coverage.

If you’d like to see how this fits your current setup, I can walk you through integration options or pilot testing. The new Twist Oncology – DNA CGP Panel provides 562-gene coverage for comprehensive tumor profiling.

Twist Tumor DNA CGP Panel

Enable improved Tx Selection and enhanced Clinical Research

Fixed Panel + Customisation Options

562 genes analyzed for SNVs and hotspot mutations (+39 genes compared to TSO500)
Microsatellite instability (MSI) detection across ~50 sites
Copy number variation (CNV) analysis for 57 clinically relevant genes
Selected fusions and tumor mutational burden (TMB) scoring for complete tumor profiling

Add custom biomarkers to differentiate your lab’s testing capabilities
Adaptable for specific clinical or research needs

End-to-End Twist NGS Workflow Compatibility:

Library preparations: EF2.0, cfDNA
Hybridization solutions with options for software analytics
Streamlined workflow for enhanced lab efficiency

Now available in Australia and New Zealand through Decode Science.

Example Data Metrics

Example sequencing QC metrics averaged across data down sampled to 2000x raw coverage (32M 2×150 reads). 4.5 Gb of Data is enough for VAF detections ranging ~2%. Data available upon request.

Panel target size	2.4 Mb
Example input	50 ng
Mean Target Coverage	515x
On-Target Rate	77%
Fold-80 Base Penalty	1.32
Duplication Rate	20%
Target bases covered >100x	99.5%

Advantages of Twist Oncology Panel

CONTENT

TSO-500 : Content is locked at 523 genes in 2025 and beyond

Twist CGP : Offers an updated CPG panel of 562 genes with Twist dsDNA probes

CUSTOMISATION

TSO-500 : Not Possible

Twist CGP : Can easily modify content to add genomic features or new biomarkers

COMPATIBILITY

TSO-500 : Product is locked into Illumina Platform Ecosystem

Twist CGP : Twist can enable Illumina short-read platforms and non-Illumina platforms (Ultima, Element, etc.)

WORKFLOW

TSO-500 : Requires an overnight capture + 2nd Hybridization Capture

Twist CGP : Single overnight hybridization capture (Option Trinity on Element)

COMPETITIVE PRICING

TSO-500 : High cost per sample for IVD kit pricing

Twist CGP : Can offer competitive pricing and modular kit options.

MODULAR PRODUCT

TSO-500 : Purchase is an all inclusive kit, no option for purchasing components

Twist CGP : Twist can sell modules, or custom configurations through OEM services

Customer Testimonial

"At LifeStrands Genomics Australia, we rely heavily on Twist’s NGS probes and reagents across nearly all our assays... Twist’s probe design flexibility and scalability have allowed us to tailor both DNA and RNA panels that suit a wide range of solid tumours without compromising sensitivity or turnaround times. We view Twist not just as a vendor, but as a strategic partner in advancing precision oncology."

Dr. Vivek Rathi, MD MSc FRCPA

Medical Director LifeStrands Genomics Australia (Genoox User)

Ready To Order?

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

DNBSEQ-T1+

October 8, 2025/in MGI, Partners, Sequencing Platforms/by Harshita Sharma

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.

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

High Throughput Antibody Production

August 18, 2025/in Partners, Synbio Antibody, Twist/by Harshita Sharma

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

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

HEK293 Express Antibodies

From 10 business days*
1 mL and 8 mL scales available
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.

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.

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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

Cinical Oncology Has new

July 15, 2025/in Uncategorized/by Harshita Sharma

Clinical Blog Update

Updated: Clinical & Pracsoft version 4.3 upgrade and performance improvement tips

From 5 December 2024, Services Australia will no longer support AIR uploads from Clinical V4.2 or earlier.

Over 60% of MedicalDirector Clincial customers are now using version 4.3

We understand that some practices may have encountered challenges when upgrading to Clinical and Pracsoft version 4.3. To help, we’ve compiled a list of suggested actions for your organisation’s System Administrator or IT provider to work through.

If you haven’t upgrade to 4.3 yet, time is running out to remain compliant for AIR uploads from 5 December 2024. Here are some of the other features you’ll benefit from when you upgrade to Clinical & Pracsoft 4.3:

Emails can now be sent with PDF attachments, can be password protected and can be sent directly from the patients file
Revamped Smartbar (formally Sidebar) with the latest Smart Connect Care tools
Add Progress Notes from anywhere in the patient workflow, via a new floating panel
Record a patient’s gender identity and preferred pronouns
A growing range of intelligent tools and marketplace partners appearing within the Smartbar

Learn more and upgrade today

Clinical and Pracsoft version 4.3 IT performance check list

These configurations are important for running software upgrades reliably and may also help improve overall performance, which can be affected by frequent scanning or blocking of MedicalDirector software activity by your IT environment’s rules and configuration.

This broad overview is applicable to a variety of software and hardware scenarios, however should not be considered an all-encompassing solution for your specific healthcare setting. These resources attempt to cover the range of different firewall and antivirus applications available, each with their own method of handling exceptions for permitted files, folders and communications activity.

The procedures outlined for handling exceptions align with industry standards, where software vendors are expected to advise which Ports and URLs need to be accessible, and the site’s Systems Administrator is responsible for interpreting the requirements and applying them appropriately within the context of the environment they are responsible for.

We strongly recommend seeking assistance with configuring your specific firewall and antivirus software by consulting your organisation’s Systems Administrator or IT provider.

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

Author Archive for: Harshita

About Harshita Sharma

Entries by Harshita Sharma

Daina Elliott

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Dr. Ebru Boslem

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Hamza Hassan

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Dr. Ebru Boslem

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Dr. Ebru Boslem

>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

Ultra-Fast Sequencing:

Seamless Automation:

Chris Wicky

Smart & Intuitive Operation:

Reliable Data Management:

Versatility for Multi-Omics:

Comprehensive Genomic Profiling for Oncology Research

Unified Testing Platform

Actionable Insights

Cost-Effective Efficiency

Chris Wicky

High-Speed, High-Throughput Sequencing

Versatile Applications Across Clinical Genomics

Integrated DNB Make & Load Technology

Smart Configurations and Automated Analysis

Chris Wicky

High Throughput Antibody Production

Customization

Speed & Efficiency

Scalable Production

Cutting-Edge Technology

Expert Support

Know More About...

Have a question?

Clinical Blog Update

Updated: Clinical & Pracsoft version 4.3 upgrade and performance improvement tips

Clinical and Pracsoft version 4.3 IT performance check list

Let’s Find You an Application That Helps Your Research

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