The Unwritten Rules of Laboratory Life

A Joe Blogs post by Joe Roberts, PhD

When you start out in research, you’re taught the essentials: experimental design, controls, statistics, and how not to accidentally destroy expensive equipment.

What you’re not taught is that every lab, regardless of country or discipline, quietly runs on a second curriculum.

The unwritten rules.

Here are a few you only really learn by doing…

1. Experiments behave like they’re being watched

The assay that performed flawlessly for weeks will suddenly forget how to function the moment you start collecting “real” data.

Antibodies lose confidence. Cell lines become opinionated. Instruments develop personality-driven error messages.

Troubleshooting, it turns out, isn’t an occasional task, it’s a full-time relationship status.

2. You will not remember what’s in the tube

At the time, you’re certain you’ll remember exactly what “Sample 1” refers to.

Future you disagrees.

Future you is now staring at a rack of identically mysterious tubes labelled “Sample 1”, “Sample 2”, and the optimistic but unhelpful “Test”.

3. Equipment has excellent timing (and a sense of humour)

Most instruments will run perfectly for months… until a grant deadline, conference abstract, or thesis submission quietly appears on your calendar.

At that point, they become selective about functionality.

Coincidence? Possibly. Universally believed otherwise? Absolutely.

4. The Best Scientific Discussions Rarely Happen in Scheduled Meetings

Scheduled meetings are fine for alignment.

The real scientific progress tends to happen in corridors, over coffee, or while waiting for a centrifuge that still insists it has 4 minutes remaining.

Somewhere between “just thinking aloud” and “quick question”, entire projects are reshaped.

5. The manual is optional. The lab veteran is not.

Every lab has at least one person who has quietly accumulated knowledge that never made it into any official documentation.

They know which button not to press, which protocol is “technically fine but don’t tell anyone”, and how to fix things that aren’t supposed to be fixable.

Finding them early saves weeks of your life.

6. Cell culture does not respect urgency

Cells grow beautifully when you’re optimising.

The moment you scale up? They reconsider their life choices.

Experienced researchers eventually accept that biology does not respond well to deadlines or emotional bargaining.

7. Negative results are still results (eventually)

At first, negative results feel like failure.

Later, you realise they’re just data that didn’t agree with your expectations.

Some of the most useful scientific directions start with the quiet discovery that something simply doesn’t work the way you thought it would.

8. One good result is interesting. Many good results are science.

A single beautiful dataset is encouraging.

A reproducible one is convincing.

The gap between the two is where most of scientific reality lives.

9. Every Lab Has Its Own Culture

Despite performing similar research, no two laboratories operate exactly the same way.

Each develops its own traditions, routines, terminology, and preferred ways of working.

Learning a new laboratory often means learning a new culture.

10. Curiosity outlasts everything else

Techniques change. Platforms evolve. Instruments get faster and more automated.

But the driving force behind all of it stays the same: curiosity.

The best researchers don’t just follow protocols, they keep asking better questions, challenging assumptions, and exploring the unknown.

Joe’s takeaway

After working in labs across three different countries and two different hemispheres, one thing has become clear: while the science, equipment, and research questions may change, the day-to-day realities of laboratory life are surprisingly consistent.

The unwritten rules aren’t quirks to be frustrated by, they’re part of what makes experimental science what it is. They remind us that research is rarely linear, often unpredictable, and always a team effort. And more often than not, the best lessons come from experience rather than instruction manuals.

If anything, these shared experiences are a quiet reminder that wherever you are in the world, you’re part of a much larger scientific community all figuring it out together!

Until next time… happy experimenting!
Joe Blogs

Meet EYRA: Multiplexing Reimagined

A Joe Blogs post by Joe Roberts, PhD

When it comes to multiplex protein analysis, researchers need accuracy, speed, and simplicity. Traditional flow-based systems have long been the standard, but they bring challenges: sheath fluids, blocked probes, and constant maintenance. Enter the Mabtech EYRA™ – a fluidics-free multiplex immunoassay platform that reimagines how scientists generate cytokine and biomarker data. With confocal imaging, RAWsphere analysis, and compatibility with EYRAplex bead kits, EYRA makes multiplexing faster, simpler, and more reliable.

Mabtech EYRA is now available in Australia and New Zealand

 

Multiplex Without Compromise

With EYRAplex magnetic bead assays, EYRA can quantify more than 30 analytes from a single sample – whether that’s serum, plasma, or cell culture supernatant. This means less sample consumption, fewer runs, and richer datasets for every experiment.EYRAplex assay schematic

At the core of EYRA’s precision is the RAWsphere image analysis algorithm. It identifies each bead, links it to the correct analyte, and quantifies the PE signal with high resolution. Whether you’re measuring six cytokines or a full 30+ panel, RAWsphere ensures your multiplex data is accurate and reproducible.

Watch video to see how EYRA works

Fluidics-Free Technology

EYRA is built around a completely flow-free design. No sheath fluid, priming, waste handling or blocked probes.

Instead of pushing samples through fluidics, EYRA uses confocal microscopy to image settled magnetic beads directly in the wells of a 96-well plate. Each bead carries a unique fluorescent dye signature for identification, while analyte-bound PE-labelled antibodies provide the quantitative signal.

The result? You insert your plate, select your assay in the intuitive Mabtech Opal™ software, and hit read. Fifteen minutes later, you have fully processed data – with your samples never leaving the wells.

From Plate to Excel - Fast

Opal™ software comes preloaded with templates for every EYRAplex kit. Standards, plate layouts, and gating are handled automatically – so you spend less time setting up and more time on results.

Once the plate read is complete, results are exported directly into Excel, with options for bulk export if you’re working on large studies or multiple plates. No manual reformatting. No data wrangling headaches.

The Maintenance-Free Mindset

Because EYRA is fluidics-free, there’s no daily calibration or cleaning. No flushing, no wasted consumables, and no time lost to instrument downtime. It’s genuinely a plug-and-play experience – switch it on, run your plate, and walk away with your data.

Joe’s Takeaway

The Mabtech EYRA isn’t just another multiplex platform – it’s multiplexing reimagined. By removing fluidics and harnessing high-resolution confocal imaging, EYRA delivers:

  • High-plex capacity: 30+ analytes per well
  • Fast turnaround: ~15 minutes per plate
  • No maintenance: no daily cleaning or calibration
  • Accurate, reproducible results: powered by RAWsphere analysis

For labs looking to streamline their workflow without sacrificing data quality, EYRA offers a fresh, frustration-free alternative to traditional flow-based systems.

Until next time… happy experimenting!

Joe Roberts, PhD
Product Manager
Millennium Science

Joe Blogs

10x Genomics Grant Application Resources

Why 10x Genomics?

10x Genomics is a proven leader in single cell research, expanding access to single cell with optimised protocols, end-to-end support, and easy-to-use analysis tools. 10x Genomics’ technology – backed by 10 years, over 2,200 patents, and > $1.5B in R&D investment – has empowered researchers to publish over 8,000 studies, including many high-impact applications of their tools.

10x Genomics’ complementary Visium and Xenium platforms offer an essential balance between unbiased discovery and precision insights and are leading the way in performance, flexibility, and ease-of-use. Being at the nexus of spatial biology means seeing what others may have missed: global cell-type organisation, cell–cell interactions, heterogeneous spatial niches, novel gene programs, critical ligand–receptor signalling networks, and spatial biomarkers of therapeutic response.

Download grant application resources here:

Enhance your chances of obtaining research funding for your Single Cell and Spatial Transcriptomics projects with the below 10x Genomics grant application resources.

Single Cell

Gene Expression

Single Cell Gene Expression

Download

Single Cell Multiome ATAC

+ Gene Expression

Multiome ATAC

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Visium Spatial

Gene Expression

Visium Spatial Gene Expression

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Xenium
In Situ

Xenium In SItu

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These grant application resources include:

  • Technology summaries
  • Applications
  • Workflow overviews
  • Technology Advantages
  • Validation studies & data benchmarking
  • Data processing & analysis
  • Sample & project size considerations
  • Additional resources
  • References

Book a project discussion or request a quote below:


Deeper Spatial Discovery with Visium HD 3′

Visium HD 3' is here! Explore more species - Now Shipping

Introducing 10x Genomics‘ Visium HD 3’, a novel assay for unbiased cross-species spatial gene expression profiling of fresh frozen tissue sections mounted on a standard glass slide. The Visium HD’s array has a gapless design that enables integration of unsupervised gene expression clustering data with microscope H&E images from the same tissue section, allowing precise profiling of finer anatomical features with high tissue coverage at single cell-scale resolution.

Furthermore, this novel reverse transcription-based assay generates cDNA products compatible with both short reads and long reads sequencing, extending its applications beyond gene expression analysis to enable immune profiling and the discovery of isoforms and novel transcripts on a spatial level.

Key Features

Visium HD 3’ assay, which delivers whole transcriptome spatial analysis with a 3’ poly(A) capture-based chemistry. This assay provides:

  • Flexibility to explore the spatial biology of fresh frozen samples from any species
  • De novo spatial discovery power, including isoforms, TCRs/BCRs, and SNVs
  • True single cell resolution with new cell segmentation software
  • Streamlined slide handling and high spatial fidelity powered by the Visium CytAssist instrument

Visium HD 3'

Contact us for pricing or more information

Space Ranger v4.0.1 is now live! Expand the power of Visium HD with cell segmentation

Improve cell-type resolution with nuclei expansion–based cell segmentation available in Space Ranger version 4.0 software. Importantly, Space Ranger v4.0 now supports cell and nucleus segmentation with H&E images. So you can reprocess existing Visium HD data through the new Space Ranger pipeline to derive these nuclei and cell segmentation outputs alongside the square bins

  1. Input a brightfield image of your H&E-stained tissue into the Space Ranger pipeline
  2. The software performs nuclei detection and expansion
  3. The Space Ranger pipeline outputs custom binning files viewable in Loupe Browser software

The new version can be found at: https://www.10xgenomics.com/support/software/space-ranger/latest

Some other notable features are:

  • A new UMI-based registration algorithm for Visium HD and Visium HD 3′ data.
  • You can now visualize and analyse Visium HD / Visium HD 3′ cell segmentation in Loupe Browser v9.
Explore data sets

Watch introductory webinar on-demand

Learn more about the Visium HD 3’ assay in this introductory webinar, including a Q&A with product experts.

Watch now

Build your own Visium HD 3’ experiment

Use 10x Genomics’ interactive tool to design your Visium HD 3’ experiment. Answer questions about your sample types and experimental goals, and get kit recommendations.

Start designing your experiment