Your Sample. Our Passion. Solutions to achieve reproducibility.

Your Sample. Our Passion.

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Solutions to achieve reproducibility

Reproducibility is the key word when we discuss the goal of independent replication and verification of the results of a study using the same methods, materials, and data. Challenges in reproducibility can affect error detection, quality control, cross-validation and more.

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What is your biggest challenge to success?

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Take part in the survey by providing your name and email address, add your vote and take the chance to win an engraved “Your Sample. Our Passion.” limited edition of the famous Eppendorf pipette pen. Prize draw entry is limited to one entry per person.

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Solve your reproducibility challenge

We are proud to be your expert partner, helping you to achieve reproducible results. Explore some product highlights to help you meet your challenge, and sign-up to our newsletter for regular updates.

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Safe-Lock microtubes

Reduce experimental variables by reducing sample loss. Eppendorf 1.5 mL Safe-Lock Tubes exhibit a higher centrifugation stability and a better lid closure than five other competing products.

Multipette^® & Combitips^® advanced

Achieve high-precision dispensing, independent of the flow characteristics of the liquid. Improve your reproducibility of long dispensing series with this dispenser & tips combination. Unmistakable down to the last detail.

man in lab with Eppendorf centrifuge holding bottle

High-Speed and Ultra-centrifugation

Available with a comprehensive selection of rotors and consumables, spinning your samples up to 110,000 x g. The right rotor will reduce your workflow steps, and therefore reduce your experimental variables.

New Brunswick S41i — CO₂ Incubator Shaker

Reproducibility of your results, e.g. in protein expression, highly relies on atmosphere accuracy and protection from fan-induced medium evaporation. Compare the S41i incubator shaker with your current solution.

Our solutions in action

Learning resources to help you to improve reproducibility in your lab.

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Centrifugation at 30,000 x g in plasmid DNA precipitation allows better recovery rates and shorter centrifugation times.

Thumbnail video What's Happening Inside Your Pipette? | Pipetting Tutorials | Ep. 4: Pipetting Systems

What is the difference between positive displacement (like the Multipette^® ) and air-cushion liquid handling systems?

Consistent conditions reduce variability and inconsistencies between DNA libraries. Learn how to achieve fast and efficient DNA purification on a single, versatile high-speed centrifuge.