Alfa Cytology - Cancer Drug R&D Services

Immunoassays Service

Inquiry

Immunoassays are fundamental analytical tools in preclinical and clinical drug development, enabling the high-sensitivity and high-specificity detection, quantification, and characterization of proteins and biomolecules based on the principle of antigen-antibody specific recognition. Alfa Cytology provides comprehensive immunoassay services to support target validation, pharmacodynamic assessment, immunogenicity evaluation, and biomarker discovery across your oncology drug development programs.

Introduction to Immunoassays

Immunoassays serve as a critical analytical bridge connecting molecular-level protein information with functional biological outcomes, delivering qualitative, semi-quantitative, and quantitative data that are essential for understanding drug efficacy, safety, and mechanism of action. Through diverse and well-validated immunoassay platforms, researchers can precisely measure drug concentrations in biological matrices for pharmacokinetic profiling, monitor anti-drug antibody (ADA) and neutralizing antibody (Nab) responses for immunogenicity risk assessment, track disease-relevant or pharmacodynamic biomarkers to support patient stratification, and visualize target protein expression levels, post-translational modifications, as well as protein-protein interactions to elucidate mechanisms of action. These data directly support lead compound screening, dose-escalation decisions, toxicity mitigation strategies, and clinical trial design, providing indispensable analytical evidence that ultimately accelerates the translational path from drug discovery to clinical application.

Fig. 1 Profiling protein expression using microfluidic western blotting in circulating tumour cells. (Budhbaware T, et al.; 2024)

Our Services

Leveraging the technology platforms of its Tumor Microenvironment Research Center, Alfa Cytology provides comprehensive immunoassay services designed to precisely profile, quantify, and track immunological events throughout the course of cancer therapy. Whether your drug candidates are small-molecule targeted modulators or large-molecule biologics, our immunoassay platforms deliver accurate data on target binding, functional activity, and microenvironmental immune responses, enabling comprehensive evaluation of the biological effects of your therapeutics in vivo.

Our immunology platform utilizes ELISA as the core quantitative tool, Western Blot as the fundamental validation method, IP/Co-IP for dissecting protein interaction networks, EMSA and ChIP for in-depth investigation of transcriptional regulatory mechanisms, and monoclonal antibody production to ensure the supply of critical reagents—forming a complete technological closed loop from tool development to mechanistic validation.

Test Types

Western Blot

We provide full-service Western Blot detection covering the entire workflow from sample preparation to data interpretation, supporting all stages of drug development including target validation, pharmacodynamic evaluation, and mechanistic studies. Our services encompass:

  • Target protein expression level detection
  • Drug-induced protein expression change analysis
  • Post-translational modification detection
  • Protein molecular weight and splice variant analysis
  • Subcellular localization-assisted analysis

Immunoprecipitation and Co-Immunoprecipitation (IP and Co-IP)

Under non-denaturing conditions, we selectively enrich target proteins and their physiological binding partners from complex lysates, specifically designed for target confirmation and signaling pathway dissection to facilitate drug target validation and mechanistic elucidation. Services include:

  • Target protein immunoprecipitation (IP)
  • Protein-protein interaction validation (Co-IP)
  • Indirect target-drug binding verification

Electrophoretic Mobility Shift Assay (EMSA)

Employing a native polyacrylamide gel electrophoresis system, we objectively evaluate the affinity between transcription factors and DNA cis-elements, providing direct evidence for drug intervention in transcriptional activity. Our service offerings encompass:

  • Transcription factor-DNA binding activity detection
  • Comparative analysis of binding activity before and after drug treatment
  • Precise mapping of core cis-element motifs
  • Supershift/antibody interference validation

Chromatin Immunoprecipitation (ChIP)

Utilizing in vivo crosslinking and chromatin fragmentation techniques, we faithfully reflect the binding status of nuclear proteins to DNA regulatory regions, facilitating studies on transcriptional regulation and epigenetic mechanisms. Our key application areas include:

  • Transcription factor target gene identification
  • Histone modification dynamics analysis
  • RNA polymerase II occupancy detection
  • Epigenetic drug target validation

Enzyme-Linked Immunosorbent Assay (ELISA)

We offer comprehensive ELISA services from method development to sample analysis, supported by a high-sensitivity, high-specificity platform for pharmacodynamic evaluation, immunogenicity testing, and biomarker monitoring. Services include:

  • Method development and established method validation (Non-GLP)
  • PK sample analysis in large/small animals
  • ADA (Anti-Drug Antibody) and Nab (Neutralizing Antibody) analysis
  • Ligand Binding Assay (LBA)
  • Biomarker quantification

Monoclonal Antibody

Focused on novel tumor targets and scarce antigen scenarios, we employ classical hybridoma technology with fully controllable delivery throughout the process. Our service workflow includes:

  • Antigen design and preparation
  • Animal immunization and titer monitoring
  • Hybridoma fusion and monoclonal screening
  • Antibody isotyping and specificity characterization
  • Large-scale production and purification

Supported Therapeutic Modalities

Our immunoassay services broadly support diverse cancer therapy R&D, delivering precise quantitative and qualitative immunological data for target engagement validation, immunogenicity risk assessment, pharmacodynamic monitoring, and mechanistic elucidation to inform your critical R&D decisions.

Available Model Systems and Biological Matrices

Our immunoassay services are applicable to a wide range of cancer research models, providing reliable immunological data support for target validation, pharmacodynamic evaluation, and immunogenicity assessment across different stages of drug development.

Applications of Our Immunoassays Service

Target Discovery and Validation

Multi-layered evidence linking potential targets to disease biology and therapeutic sensitivity through integrated application of Western Blot (protein expression confirmation), Co-IP (interaction partner identification), ChIP (target gene recognition), and EMSA (DNA binding activity validation) to support advancement of target pipelines.

Pharmacodynamics and Biomarker Monitoring

For small molecules, Western Blot quantifies target protein expression and modification levels to reflect target inhibition efficiency, while ELISA quantifies effector biomarkers to provide PD evidence for dose optimization and decision-making; for large molecules, ELISA ligand binding assays quantify serum drug concentrations, and bridging ELISA monitors ADA/Nab dynamics to assess immunogenicity risk.

Mechanism of Action and Transcriptional Regulation Studies

EMSA evaluates drug effects on transcription factor DNA binding capacity, ChIP reveals drug-induced changes in transcription factor genomic occupancy and histone modification patterns, and Co-IP verifies whether drugs interfere with protein complex assembly, collectively elucidating candidate drug mechanisms from multiple dimensions.

Protein Interaction Network Dissection

Systematic IP/Co-IP experiments construct target-related protein interaction networks, validate physical associations between targets and downstream effector molecules, identify novel interaction partners to reveal potential resistance pathways, and provide scientific rationale for combination therapeutic strategies.

Alfa Cytology offers comprehensive immunology services encompassing cytokine profiling, immune cell phenotyping, T-cell function assays, ADCC/CDC evaluation, and immuno-modulatory activity screening. Our solutions support small molecule drugs, therapeutic antibodies, cell and gene therapies, cancer vaccines, and oncolytic viral therapies, with customizable options ranging from single assays to integrated R&D packages. Please don't hesitate to contact us to learn how our integrated immunoassay services can accelerate your oncology drug development programs.

Reference

  1. Budhbaware T, et al. Molecular methods in cancer diagnostics: a short review. Ann Med. 2024;56(1):2353893.

For research use only.

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