Nuclera

Nuclera

On-demand gene-to-protein synthesis platform

Overview

Nuclera provides on-demand gene and protein synthesis for researchers in synthetic biology, enabling writing of genes and proteins directly in benchtop laboratories. Its platform translates genetic designs into physical DNA and expressed proteins quickly, often within a day, by selling a benchtop synthesis platform and related consumables to labs and institutions. The workflow lets users design sequences and order synthesis or run gene-to-protein construction with high speed, flexibility, and accuracy. Nuclera aims to democratize biology by making gene and protein writing accessible and customizable, so researchers can design, build, and engineer biology in their own labs.

Significant Headcount Growth

About Nuclera

Simplify's Rating
Why Nuclera is rated
B-
Rated B on Competitive Edge
Rated B on Growth Potential
Rated C on Differentiation

Industries

Industrial & Manufacturing

Biotechnology

Healthcare

Company Size

51-200

Company Stage

Series C

Total Funding

$224.9M

Headquarters

Cambridge, United Kingdom

Founded

2013

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Simplify's Take

What believers are saying

  • January 2026 funding extension and May 2026 launches signal strong investor and product momentum.
  • APAC and Middle East distribution broaden sales reach beyond UK and US buyers.
  • 48-hour GPCR panels and antibody screening tap high-value drug-discovery bottlenecks now.

What critics are saying

  • Only $87 million funding must fund commercialization, product expansion, and global support.
  • AI-driven antibody triage commoditizes quickly if Thermo Fisher or Cytiva bundles similar workflows.
  • If eProtein Discovery misses reproducibility, academic installs stall and Nuclera becomes a niche reagent vendor.

What makes Nuclera unique

  • eProtein Discovery compresses protein expression, purification, and validation into one benchtop workflow.
  • Nuclera now covers antibodies, membrane proteins, and GPCRs across one platform.
  • leadXpro and Cytiva partnerships validate Nuclera as a workflow layer for discovery labs.

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Funding

Total Funding

$224.9M

Above

Industry Average

Funded Over

10 Rounds

Series C funding is usually for startups that are doing well and are looking for more money to fuel major growth, such as acquiring other companies, expanding into global markets, or launching new product lines. Investors typically include larger venture capital firms and private equity.
Series C Funding Comparison
Below Average

Industry standards

$50M
$12M
Nuclera
$40M
Figma
$50M
Medium
$62M
SeatGeek
$100M
Oura

Benefits

Health Insurance

Dental Insurance

Vision Insurance

Life Insurance

Disability Insurance

401(k) Retirement Plan

Paid Holidays

Professional Development Budget

Stock Options

Company Social Events

Growth & Insights and Company News

Headcount

6 month growth

4%

1 year growth

7%

2 year growth

5%
Bio-IT World
May 10th, 2026
Nuclera launches antibody triage service to advance AI-driven antibody discovery.

Nuclera launches antibody triage service to advance AI-driven antibody discovery. May 10, 2026 Rapid binder triage, of AI-driven candidate sets, enables early elimination of non-binders ahead of costly downstream workflows Powered by cell-free technology to convert AI-generated candidates into experimental binding data Cambridge, UK and Boston MA, USA 11 May 2026: Nuclera, the biotechnology company enabling rapid access to high-quality proteins, today announced the launch of its antibody screening service to streamline the transition from antibody hit generation to lead selection. The service will support researchers seeking to identify the most promising antibody candidates to progress to costly mammalian expression and functional testing, addressing a key bottleneck in AI-driven antibody discovery. The launch follows the Company's Series C extension[1], enabling the integration of antibody expression and binding validation to support antibody discovery workflows. Nuclera's antibody service delivers a rapid upstream triage workflow that identifies viable binders early on in the process between in silico hit generation and mammalian scale-up. By utilizing 96-plex binary cell-free expression and binding assays, the service screens full length antibody libraries in parallel, rapidly narrowing large candidate sets to a focused subset of confirmed binders. Surface Plasmon Resonance is then performed on prioritized hits for binding kinetics. Despite advances in bioinformatics and in silico antibody design, a major bottleneck remains in experimentally validating large numbers of candidates. Traditional antibody secondary screening methods are often slow and fragmented, which typically result in large amounts of resources being spent on non-binders through costly processes. As AI-driven approaches generate increasingly large antibody libraries, the need for rapid, cost-effective triage solutions has become more critical. Nuclera's antibody service addresses this gap by converting large AI-generated libraries into experimental binding data and enabling early elimination of non-binders, reserving expensive downstream biology for candidates proven to bind and accelerating progression to validated leads. Dr Michael Chen, CEO and co-founder, Nuclera, said: "Antibodies are one of the most important classes of therapeutic molecules, yet antibody discovery remains inefficient, with many initially promising candidates failing during downstream validation. A key bottleneck is the cost of recombinant antibody expression and binding validation, which limits the generation of high-quality data, and is holding back the full potential of AI/ML discovery. The launch of our antibody service addresses this challenge by enabling rapid triage of large candidate sets and delivering decision-grade binding data early in the discovery process at a competitive cost. By helping teams focus on the most promising candidates before scale-up, we are taking an important step toward enabling more effective use of AI in antibody discovery." Media contact: Dr Ben Rutter Zyme Communications Tel: +44(0)7920 770 935

Yahoo Finance
Mar 30th, 2026
Nuclera launches GPCR nanodisc panel producing active proteins in 48 hours

Nuclera has launched a nanodisc panel to accelerate G-Protein Coupled Receptor (GPCR) production, enabling expression of active GPCRs in 48 hours. The panel includes a GPCR screen kit and scale-up reagents featuring eight nanodisc combinations with two membrane scaffold proteins and four lipid compositions. The technology addresses a critical bottleneck in drug discovery, as obtaining purified, stable, functional GPCRs remains challenging despite one-third of FDA-approved drugs targeting these receptors. Traditional detergent-based methods often cause proteins to adopt non-native conformations, whilst Nuclera's nanodiscs provide a soluble membrane bilayer that better maintains structural integrity. The panel integrates with Nuclera's eProtein Discovery cell-free protein synthesis platform, enabling co-translational insertion for higher yields of soluble, active membrane protein. The company launched its membrane protein workflow in 2025.

Cambridge Network
Mar 30th, 2026
Nuclera launches gpcr-focused nanodisc panel to streamline membrane protein production.

Nuclera launches gpcr-focused nanodisc panel to streamline membrane protein production. * Enables expression of active GPCRs in 48 hours * Panel supports screening to scale-up on eProtein Discovery Cambridge, UK, and Boston MA, USA, 30 March 2026: Nuclera, the biotechnology company enabling rapid access to high-quality proteins, today announced the launch of its nanodisc panel to support screening and scale-up of G-Protein Coupled Receptors (GPCRs). Building on the eProtein Discovery(TM) membrane protein workflow capabilities[1], the nanodisc panel allows membrane protein scientists focusing on GPCR research to identify optimal membrane environments and increase production of challenging therapeutic targets, GPCRs, producing active proteins in 48 hours. Nuclera's nanodisc panel includes a GPCR screen kit and scale-up reagents, including 8 nanodisc combinations, comprised of 2 membrane scaffold proteins (MSPs), and 4 lipid compositions. Allowing researchers to rapidly and cost-effectively express active GPCRs, the nanodisc panel minimizes variability associated with traditional approaches to membrane protein production. The preassembled nanodiscs target the specific charge, fluidity and/or cholesterol requirements for GPCR activity and yield. Despite one third of FDA-approved drugs acting on GPCRs[2], obtaining purified, stable, functional GPCRs remains a critical bottleneck in pharmacology and drug discovery. Traditionally, cell-based detergent micelles are used to solubilize membrane proteins, but often lead to proteins adopting non-native conformations. Nanodiscs provide a soluble membrane bilayer allowing the study of membrane proteins and their interactions under native-like conditions better maintaining structural integrity and in vivo functionality compared to detergent-based approaches. Integrating Nuclera's pre-assembled nanodiscs directly into eProtein Discovery's cell-free protein synthesis (CFPS) approach enables co-translational insertion of the nascent protein. This delivers high yields of soluble, active membrane protein with improved stability for downstream applications and streamlines drug discovery workflows from screening to characterization. Dr Audrey Dubourg, Product Manager, Nuclera, said: "Since releasing our membrane protein workflow in 2025, we have identified a huge potential in the market to support GPCR protein scientists. Our eProtein Discovery(TM) nanodisc panel empowers researchers to explore physiologically relevant environments validated for solubility, insertion and stabilization of membrane proteins. Compared to traditional approaches, these are capable of increasing protein yield whilst maintaining functionality, creating a fast-track route to purified, active GPCRs." Dr Michael Chen, CEO and co-founder, Nuclera, commented: "The release of our GPCR nanodisc panel addresses the pressure scientists face to rapidly produce functional membrane proteins. Integrated with eProtein Discovery, this capability equips researchers with a powerful approach to increase success rates in expressing active GPCRs."

Cambridge Innovation Capital
Mar 29th, 2026
Nuclera and TRIMTECH Therapeutics success at the One Nucleus Awards 2026.

Nuclera and TRIMTECH Therapeutics success at the One Nucleus Awards 2026. 29 Mar 2026 Many congratulations to all of the winners and finalists, including portfolio compnaies Nuclera and TRIMTECH Therapeutics The winners of the One Nucleus Awards 2026 were announced at an awards ceremony in London on 29 March. The One Nucleus Award categories are structured to reflect that breadth of R&D, investment, service provision and enabling support across the stakeholders. Best Therapeutic R&D Programme of the Year | Winner: Resolution Therapeutics | Finalists: Serenatis Bio, TRIMTECH Therapeutics Best Use of Emerging Technology of the Year | Winner: Nuclera | Finalists: Ignota Labs, Constructive Bio

Cambridge Innovation Capital
Mar 18th, 2026
Portfolio company Nuclera has been ranked in the top 10 of this year's Sifted 100: UK & Ireland leaderboard.

Portfolio company Nuclera has been ranked in the top 10 of this year's Sifted 100: UK & Ireland leaderboard. Sifted 18 Mar 2026 Rising an impressive 37 places from last year to secure 10th position, Nuclera recorded the largest year-on-year climb across the entire ranking. This recognition underscores Nuclera's growing impact as one of the leading companies driving economic growth and innovation in an increasingly competitive landscape. Sifted 100: UK & Ireland (2026) Welcome to the third annual Sifted 100: UK & Ireland Leaderboard, which ranks the region's 100 fastest-growing startups and scaleups by revenue growth over the past three financial years. Together, these 100 companies have raised £18.4bn in funding, generated £2.6bn in revenue over the last three years and now employ around 10,750 people across the UK and Ireland. Notably, £1.7bn of that revenue was generated in the most recent year alone, underscoring just how quickly these startups are scaling. To be eligible, startups had to be private, independent and headquartered in the UK or Ireland, with the majority of revenue generated from proprietary technology. Companies must have been founded in or after 2010, and have at least three years of revenue data (from 2022-2024, 2023-2025 or 2024-2026), covering accounting periods of at least 26 weeks. Revenue had to be at least £42k in the base year and £420k in the most recent year. Companies were required to submit signed documentation to verify any financial data not publicly available. Some opted to keep parts of this information confidential. Read the accompanying research report, featuring interviews with 20+ founders and investors, as well its ranking of the 100+ investors and lenders with at least two companies on the leaderboard.

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