Reimagining Immunoassays With End-to-End Integrated Solutions
Whitepaper
Published: September 9, 2025
Credit: Revvity
Immunoassays are essential for detecting and quantifying specific molecules, identifying and characterizing biomarkers, supporting therapeutic discovery, and assessing drug safety and function throughout the development pipeline.
Yet traditional immunoassay workflows face critical challenges, including inconsistent results, fragmented processes and mounting budget constraints that can compromise research outcomes and productivity.
This whitepaper explores how comprehensive immunoassay ecosystems can address these limitations by integrating instruments, reagents, automation and software into cohesive solutions that streamline workflows from sample preparation to data analysis.
Download this whitepaper to discover how to:
- Address inconsistent results, process fragmentation and budget constraints
- Integrate end-to-end workflows from sample prep to data analysis across multiple assay formats
- Maximize research ROI by enhancing productivity and accelerating discovery timelines
W H I T E PAPER
Reimagining immunoassay workflows:
The integrated future of discovery
Imagine a scenario where samples moved efficiently
from preparation to analysis, with minimal manual
intervention, optimized protocols, and real-time data
capture. Revvity’s comprehensive immunoassay
ecosystem transforms this vision into reality by integrating
instruments, reagents, services, and support into a cohesive,
customizable solution. From assay design to data analysis,
Revvity’s solutions are designed to help streamline
each stage of the workflow, with the goal of enhancing
efficiencies, reducing sources of variability, and improving
the potential for insightful research outcomes.
In this article, we outline the key challenges facing
immunoassay workflows and demonstrate how Revvity’s
integrated solutions are designed to address these
limitations and promote consistency, efficiency, and
cost-effectiveness across the entire workflow.
The immunoassay integration challenge
Immunoassays play a central role across the life sciences,
from academic and pharmaceutical research to the work of
both Contract Research Organizations (CROs) and Contract
Development and Manufacturing Organizations (CDMOs).
These assays are essential for detecting and quantifying
specific molecules, identifying and characterizing
biomarkers, supporting therapeutic discovery, and assessing
drug potency, safety, and function throughout the discovery,
development, and manufacturing pipeline.
However, immunoassay workflows often encounter
multiple challenges. Among these are inconsistent results,
fragmented workflows, data management and interpretation,
and growing budget constraints. Whether in academia,
pharma, or contract services, these challenges can disrupt
productivity and compromise outcomes.
Challenges in immunoassay integration
Challenge Problem Impact
Inconsistent results Lack of reproducibility across
platforms and studies
• Data confidence undermined
• Slower decision making
• Regulatory hurdles
• Research delays
Fragmented workflows Disconnected processes from
sample prep to analysis
• Increased turnaround time
• Reduced data integrity and traceability
• Higher error rates and inconsistencies
• Inefficiencies in high-throughput environments
Budget constraints High costs limit scalability and
flexibility
• Limited operational scale
• Slow adoption of innovation
• Talent retention challenges
Table 1: Challenges in immunoassay integration
Reimagining immunoassay workflows: The integrated future of discovery
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Inconsistent results
Immunoassays offer tremendous value across research
and clinical applications, although their full potential
is best realized when assay conditions, reagents, and
platforms are properly optimized and calibrated. Without
this optimization, lack of concordance across platforms
can make it difficult to interpret data with confidence,
ultimately hindering research continuity, slowing down
decision making, and complicating data interpretation for
regulatory submissions.
Inconsistencies can arise from several sources. First,
immunoassay designs can vary considerably, from the
choice of detection method to the assay format, which
influences performance characteristics. Reagent quality
and manufacturing variability play important roles in
reliable outcomes, as lot-to-lot variations can affect
assay sensitivity or signal output. Standardized calibration
methods and procedures across platforms enable more
effective comparisons across studies or transitions
between technologies while biological interferences, such
as endogenous immunoglobulins or heterophile antibodies,
can distort assay signals and further skew results. And
finally, human factors are a continuous source of variability.
Pipetting techniques, incubation times, and sample handling
can all impact results, especially in manual workflows.
These inconsistencies all represent real risks to productivity
and decision-making processes.
Fragmented workflows
In addition to technical variability, traditional immunoassay
workflows are often fragmented, involving multiple
manual steps and specialized instruments. Again, this
fragmentation stems from several factors. Manual handling
of samples and reagents can increase the likelihood of
errors such as pipetting mistakes, reagent contamination,
or sample mislabeling. These time-consuming steps add
variability to workflows, particularly in high-throughput or
multi-site settings where consistency is key. Additionally,
using multiple standalone instruments, each with its own
operating protocols and data formats, creates obstacles
to workflow optimization and data consolidation.
By streamlining these processes, from sample preparation
to data analysis, laboratories can enhance efficiency,
reduce potential errors, optimize turnaround times, and
strengthen data integrity.
Budget constraints
The final—and often most pressing—challenge is budget
constraints. As organizations across the academic,
pharmaceutical, and contract research sectors face
increasing pressure to do more with less, the financial
implications of traditional immunoassay workflows become
a major consideration. These workflows can be resource
intensive due to the need for multiple instruments tailored
to different assay types or detection methods. Maintaining a
suite of specialized instruments can be expensive, not only
in terms of upfront costs but also ongoing maintenance and
calibration. Furthermore, each will require its own reagents,
calibration protocols, and maintenance schedules, driving
up costs especially when scaling up experiments.
Beyond the equipment, there is a significant human resource
investment, with each instrument and experiment requiring
dedicated and/or highly-trained personnel. Recruiting,
training, and retaining this expertise can be both time
consuming and resource intensive, especially in an industry
where skilled talent is in high demand. This fragmented,
resource-heavy approach can make it difficult for
organizations, big or small, to scale operations efficiently or
respond quickly to shifting project demands.
These challenges of variability, fragmentation, and budget
pressure don’t exist in isolation. They intersect across every
stage of the immunoassay workflow, potentially introducing
risk, variability, and operational inefficiencies. Addressing
these issues not only requires making incremental changes;
it necessitates rethinking how immunoassays are designed,
integrated, and executed across the entire workflow. In an
environment where funding and budgets are constrained,
the need for more streamlined, cost-effective solutions has
never been more relevant.
The integrated approach
As research demands grow and budgets tighten, a more
integrated immunoassay strategy offers a promising
avenue to address the challenges discussed earlier,
enhancing efficiency, consistency, and scalability in the
lab. By combining advanced instrumentation, standardized
protocols, and expert support, these integrated solutions
empower researchers to produce high-quality, reproducible
data more quickly and with fewer resources.
Reimagining immunoassay workflows: The integrated future of discovery
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Key benefits of an integrated immunoassay
workflow include:
Enhanced consistency: Standardized platforms and assay
protocols reduce variability, leading to more reliable and
reproducible results.
Streamlined workflows: Automation and integration
minimize the need for manual steps, reducing the risk
of errors, shortening turnaround times, and freeing up
personnel for more high-value tasks.
Cost efficiencies: Consolidating workflows helps lower
costs by reducing the number of instruments needed,
simplifying training, and optimizing resources and
reagent use.
In the following sections, we’ll explore how immunoassay
technologies have evolved and how Revvity’s
integrated ecosystem is redefining what’s possible in
immunoassay research.
The evolution of immunoassay technology
The journey of immunoassay technology began in the late
1950s with the development of the radioimmunoassay by
Rosalyn Yalow and Solomon Berson.1 This groundbreaking
method, which relied on the use of radioactive isotopes
to quantify antigen-antibody interactions, earned Yalow
the Nobel Prize in Physiology or Medicine in 1977.
A major breakthrough followed in the early 1970s with the
introduction of the Enzyme-Linked Immunosorbent Assay
(ELISA),2 which replaced radioactive labels with enzymes,
offering a safer and more practical approach for detecting
antigens and antibodies.
As scientific questions have grown more complex,
so too have the demands on immunoassay systems.
Over the decades, ELISA has undergone substantial
refinement, incorporating numerous enhancements such
as chemiluminescent and fluorescent substrates that
dramatically increased sensitivity and reduced assay times.
Today, researchers have access to a diverse array of
immunoassay formats, including multiplexed assays and
fully automated systems, that reduce manual handling,
increase throughput, and expand analytical capabilities.
How Revvity advances the modern workflow
Building on decades of experience, Revvity is reshaping
immunoassay workflows by delivering solutions that
address the core challenges of inconsistency, fragmentation,
and cost inefficiency.
Comprehensive portfolio
Revvity’s immunoassay offerings span from traditional
ELISAs to more innovative no-wash and flow-based
platforms. These flexible formats are optimized for
compatibility across various multimode reading instruments
and applications, supporting a wide range of research needs
across different scientific disciplines.
No-wash immunoassays
Recognizing the challenges of manual wash steps in ELISA,
Revvity has developed multiple no-wash immunoassay
technologies including HTRF™, AlphaLISA™, and
LANCE™ Ultra™. These platforms streamline workflows,
reduce variability, and are particularly well-suited for highthroughput
screening applications.
Integrated solutions
Beyond individual assays, Revvity offers customizable
integrated workstations with preset protocols that enhance
both efficiency and sensitivity. These end-to-end solutions
encompass assay design, automation, data analysis, and
expert support, ensuring a cohesive workflow from sample
to result.
Revvity’s complete ecosystem approach
While innovations in individual technologies, such as
detection, automation, or assay platforms, can improve
isolated steps of the workflow, the real wins come from
a fully integrated system where every component is
designed to work cohesively with others. As shown in
Figure 1, Revvity’s end-to-end immunoassay ecosystem
brings together instruments, reagents, automation, and
software to create a seamless, cohesive workflow from
sample to insight.
The following section explores each area—sample
preparation, assay execution, detection, automation, and
data analysis—illustrating how, when these tools are used
together, they not only simplify workflows but also multiply
their effectiveness.
Reimagining immunoassay workflows: The integrated future of discovery
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Figure 1: Revvity’s integrated immunoassay ecosystem illustrates how each component—from sample preparation through to data
analysis—works together to create a seamless workflow designed to enhance reproducibility, efficiency, and data quality.
Sample preparation
Workflow challenge: Sample preparation variability.
Ensuring quality starting material through effective
homogenization and lysis.
Sample preparation represents a foundational first
step in successful immunoassay workflows. Effective
homogenization, the process of breaking down biological
samples into a uniform mixture, is essential to ensure
consistent lysis and analyte extraction from samples.
Samples are not limited to tough tissues, but complex
matrices such as cell cultures and biological fluids where
researchers may want to shy from harsh chemicals
or enzymes. Incomplete homogenization and lysis can
introduce significant variability, potentially compromising
the integrity and analytical reproducibility of the data.
Revvity solution: Advanced homogenization technologies
Revvity addresses these challenges through a suite
of offerings designed to support efficient and reliable
processing across both small-scale studies and
high-throughput workflows. Omni Bead Ruptor™ bead
mill homogenizers leverage the power and consistency
of mechanical shearing by bead-beating that maximizes
tissue disruption and cell lysis in a sealed vessel, making
them highly effective for tough, complex, or fibrous
samples. For labs who prefer rotor-stator technologies
for certain applications, Omni mixers and handheld/standmounted
homogenizers offer efficient, tunable processing,
especially when coupled with Omni Tip™ disposable
probes to significantly minimize risk of cross-contamination.
Importantly, these solutions build the foundation for Omni
automated workstations that seamlessly integrate into
high-throughput workflows significantly reducing operator
variability and giving time back to the researcher for
complex tasks. Revvity offers a path to standardize and
scale upstream sample prep that’s conducive to the success
of downstream immunoassay performance, enhancing the
analytical sensitivity, specificity, and overall reproducibility
of results.
Assay execution
Workflow challenge: Diverse research requirements.
Selecting the optimal immunoassay format for
specific applications.
Today’s researchers can choose from a diverse array of
immunoassay technology platforms, each optimized for
specific research applications. The ideal assay format
depends on several factors, including the target analyte,
required sensitivity, sample type, multiplexing needs, and
overall throughput requirements. Additional considerations
include workflow complexity, instrument compatibility, and
cost efficiency.
Immunoassays
Workflow
• ELISA
• LEGENDplex
• ELISpot
• Alpha
• HTRF
• LANCE
• DELFIA
• Omni
homogenizers
and lysis kits
• Fontus
• JANUS
• Assays
• Custom
• Multimode
plate readers
• Image
cytometers
• explorer G3
• Revvity
Signals
software
Sample
Preparation
Liquid Handling Microplate Read out Lab
Automation Analyze
Revvity Solution
Reimagining immunoassay workflows: The integrated future of discovery
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Revvity solution: Comprehensive immunoassay portfolio
Revvity offers a vast selection of immunoassay
technologies to support these varied needs, spanning
pre-configured kits to customizable reagents. Traditional
ELISA remains a reliable option for many labs, offering
robust quantification with straightforward workflows and
accessible instrumentation. As an additional wash-based
option, DELFIA™ technology combines the benefits of time
resolved fluorescence (TRF) with lanthanide chelates to
create a highly sensitive, robust, and reproducible assay
format. For those seeking enhanced sensitivity and broader
dynamic range, Revvity’s no-wash assay technologies,
including HTRF, AlphaLISA, and LANCE Ultra, provide
streamlined workflows and rapid detection with minimal
hands-on time. For multiplexing applications, LEGENDplex™
assays enable the simultaneous quantification of multiple
targets in a single sample. Additionally, the ELISpot assay
(utilizing BioLegend antibodies/reagents with T-SPOT®
technology research applications) from Revvity can achieve
highly sensitive and specific cytokine measurements of
cell-mediated immune responses at the single-cell level.
These platforms can be tailored to specific experimental
requirements or scaled for high-throughput applications
through Revvity’s customization services. By offering this
flexibility, researchers can select the optimal immunoassay
approach for everything from early discovery to advanced
therapeutic development.
Detection systems
Workflow challenge: Diverse detection requirements
Transforming biochemical interactions into reliable
quantitative data.
Detection is a critical phase in the immunoassay workflow,
offering a way to transform biochemical interactions into
quantifiable data. Multimode plate readers are essential
tools in this phase, enabling the measurement of various
biological, chemical, and physical interactions occurring
in microplate-based assays. These instruments support
a range of detection modes, including absorbance,
luminescence, fluorescence intensity, time-resolved
fluorescence, fluorescence polarization, and Alpha
technology, offering the flexibility to accommodate various
assay types.
Revvity solution: Integrated detection systems
Revvity’s portfolio of multimode microplate readers are
developed to enable results across all major detection
modes. By engineering multiple reading mode/technologies
into a single instrument, these systems allow researchers
to seamlessly transition between assay formats without
compromising performance or workflow efficiency.
They are optimized for compatibility with Revvity’s broad
assay portfolio, ensuring reliable data acquisition from
ELISA to AlphaLISA, HTRF, and other advanced assay
platforms. For high-content applications, Revvity also
offers automated cell counting image cytometers and
high-resolution imaging systems, combining quantitative
fluorescence detection with spatial cellular information.
This enables precise cell density and counting as well as
phenotypic analysis at sub-cellular level. Together, these
detection and imaging solutions enable researchers to
confidently generate high-quality data—supporting a variety
of applications and research needs.
For traditional 96-well plates, Revvity also offers the Mini
ELISA Plate Reader™, a small, compact instrument capable
of saving time and space in the lab. A single USB cord
enables plug-and-play functionality, with 96 detection units
scanning all 96 wells simultaneously. Intuitive operation
makes it easy to read your plate and obtain data at a
rapid pace.
Automation solutions
Workflow challenge: Scalability and consistency. Managing
complex workflows while minimizing variability.
As immunoassay workflows become more complex and
throughput demands increase, the ability to automate
tasks has become a critical enabler of speed, consistency,
and data quality. Manual handling—while still necessary
in certain contexts—can introduce variability and limit
scalability, bringing unwanted bottlenecks and risks to
lab processes. Automated systems help mitigate these
challenges by streamlining repetitive tasks such as sample
preparation, liquid handling, and plate processing.
Revvity solution: Flexible automation platforms
Revvity’s automation portfolio is designed to address the
diverse needs of modern laboratories, from benchtop
application-specific workstations to fully integrated,
high-throughput systems. Automated liquid handlers such
as the Fontus™ and JANUS™ platforms are engineered to
Reimagining immunoassay workflows: The integrated future of discovery
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minimize human error, reduce sample-to-sample variability,
and enhance overall workflow efficiency. For more
complex workflows, the explorer™ G3 series offers
an integrated solution, combining microplate handling,
liquid handling, detection, and imaging into a seamless
system. These flexible, scalable, and modular platforms
support a range of applications including high-throughput
screening, cell-based assays, and genomics-based
workflows. Systems can be customized to incorporate
Revvity instruments alongside third-party technologies,
offering laboratories the flexibility to design an automation
ecosystem aligned with their specific research objectives.
Data analysis
Workflow challenge: Data complexity and integration.
Extracting meaningful insights from expanding
data volumes.
Deriving meaningful insights from the large volumes of
data generated represents the culminating challenge.
As experimental designs become more complex and data
volumes increase, traditional manual analysis methods
are often impractical. Instead, advanced analysis tools are
essential, not only for efficiently processing the data, but
also uncovering patterns, trends, and correlations that might
otherwise remain hidden.
Revvity solution: Integrated informatics platform
Revvity Signals Software is the Scientific Informatics and SaaS
Platform Business for Revvity and offers one of the most
comprehensive portfolios of scientific software in the world.
The portfolio includes multiple solutions including a
cloud-based end-to-end workflow solutions providing
data capture and collaboration, data processing, and
data-driven analytics. By integrating information from
multiple departments, instruments and data sources across
the immunoassay workflow, it helps to mitigate the risk of
data silos and is designed to help researchers maintain
full context for their results. The Revvity Signals’ solution
supports a wide variety of data types and is optimized
for immunoassay workflows, including those using ELISA,
AlphaLISA, HTRF, and multiplexed technologies. By digitally
connecting every step of the workflow and structuring data
and enabling visualization—from sample preparation to
detection—Revvity Signals completes Revvity’s streamlined
approach by ensuring that valuable insights aren’t lost in the
data management process.
For the LEGENDplex multiplexing assay, BioLegend
provides a complimentary data analysis software suite
designed to analyze LEGENDplex flow cytometry data
files. The software suite consists of an online cloud-based
program as well as downloadable desktop applications for
both PC and Mac computers.
Cross sector applications and benefits
Revvity’s immunoassay ecosystem is built to deliver
measurable value across a wide range of scientific sectors.
Whether supporting discovery, advancing pipelines, or
driving client project success, Revvity offers a unified,
flexible, and future-ready workflow—connecting sample to
insight with ease.
Industry sector Value Key benefits
Academic
research
Maximize
discovery with
limited resources
• Cost-effective ELISA and no-wash assays reduce manual workload while maintaining accuracy
• Open-format compatibility supports diverse instrumentation and evolving
experimental needs.
• Comprehensive support helps preserve knowledge continuity despite academic turnover,
ensuring consistent research progress.
Pharma/
Biopharma
industry
Accelerate drug
discovery with
confidence
• High-sensitivity, scalable assays (HTRF, AlphaLISA, LANCE Ultra) optimize early screening and
lead validation.
• Open, automation-compatible formats reduce bottlenecks and enable seamless workflow
expansion.
• A single-source solution—from reagents to software—ensures reliability, efficiency, and
regulatory readiness.
CROs and
CDMOs
Deliver
consistent,
client-ready
results
• Standardized, verified immunoassays ensure reliable data across diverse client projects.
• Cross-platform compatibility supports integration with sponsor systems and third-party
instruments.
• Modular automation and end-to-end technical support enhance throughput while ensuring
compliance and data integrity.
Table 2: Cross-sector applications and benefits of Revvity’s immunoassay ecosystem
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Supporting this ecosystem is BioLegend’s expansive
portfolio of high-quality antibodies, trusted by researchers
for their performance across a broad range of research
areas. Engineered to meet diverse experimental needs,
these antibodies empower applications such as flow
cytometry, TotalSeq™ for multi-omics, microscopy,
immunoassays, and Western blotting.
For organizations seeking additional resources, Revvity
offers specialized immunoassay services through its
Preclinical Services Portfolio at the Cambridge (UK) site.
These services allow customers to access Revvity’s
immunoassay expertise and capabilities, providing a
valuable option for those who prefer outsourcing their
immunoassay needs.
Together, these solutions empower researchers across
academia, pharma/biopharma, and CROs can fully leverage
the power of Revvity’s integrated immunoassay approach to
drive future innovation and discovery.
Future outlook
As immunological research advances and precision
medicine becomes increasingly sophisticated, the future
of immunoassay workflows will be defined by seamless
integration, smarter data interpretation, and increasingly
complex biological models. From single-cell analytics to
artificial intelligence, researchers are moving towards
a deeper understanding of the immune system than
ever before. Emerging applications and technologies
include the following:
Single-cell analysis: The ability to investigate cellular
signaling and interactions at the individual cell level using
single-cell technologies will offer opportunities to better
understand immune complexity. These insights will be vital
for designing precise therapeutic antibodies, identifying
novel vaccine candidates, and developing more targeted
immunotherapies.
Multi-omics tools: The integration of genomics,
transcriptomics, and proteomics tools will provide a
more holistic view of immune function. By aligning these
approaches, researchers will be able to better understand
how molecular changes influence immune responses.
3D cell models: As cell models continue to evolve,
3D cell culture systems, such as organoids, are offering a
more physiologically relevant context for immunological
studies. These models allow researchers to explore
immune interactions at the tissue and organ levels, offering
insights into both healthy and tumor microenvironments.
When paired with high-content imaging, these models allow
researchers to quantify small immunological changes,
potentially advancing the understanding necessary for the
future development of precision therapies.
Automation: Integrating automated systems into 3D cell
culture workflows is essential to manage the added
complexity. Automating these workflows not only reduces
variability but also improves throughput and reproducibility,
enabling researchers to study cellular dynamics and immune
responses under physiologically relevant conditions.
AI and machine learning: The use of AI and machine
learning is transforming how immunoassay data is analyzed
and interpreted. Information within large, complex
datasets can be mined to uncover disease-specific immune
signatures, enhance prognostic capabilities, and support
predictive models.
Looking ahead, a more comprehensive understanding of the
immune system at the molecular and single-cell level will
be essential for progress across immunological modalities.
From vaccine development and antibody engineering to
targeted immunotherapies and host-graft compatibility,
integrated immunoassay technologies will be central to
future progress across every aspect of immune research.
Revvity’s immunoassay ecosystem integrates instruments,
reagents, automation, and software to support a
streamlined workflow from sample preparation through
to data analysis. This approach is designed to improve
reproducibility, reduce variability, and enable researchers
to generate high-quality data across a broad range of
immunological applications.
Reimagining immunoassay workflows: The integrated future of discovery
For research use only. Not for use in diagnostic procedures. 1909502
www.revvity.com
Copyright ©2025, Revvity, Inc. All rights reserved.
Revvity is a trademark of Revvity, Inc.
All other trademarks are the property of their respective owners.
References
1. Yalow RS, Berson SA. Immunoassay of endogenous plasma insulin
in man. Journal of Clinical Investigation 1960; 39: 1157–1175.
2. Engvall E, Perlmann P. Enzyme-linked immunosorbent assay
(ELISA) quantitative assay of immunoglobulin G. Immunochemistry
1971; 8: 871–874.
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