CD BioSciences provides expert AlphaScreen binding assay services for highly sensitive, no-wash detection of biomolecular interactions. Our AlphaScreen platform is ideal for studying weak interactions, large complexes, and high-throughput screening applications, offering exceptional sensitivity and ease of use for epigenetic and drug discovery research.
AlphaScreen is a versatile, bead-based technology that enables the detection of molecular interactions in a homogeneous, "mix-and-measure" format. The assay relies on donor and acceptor beads that, upon illumination at 680 nm, produce a cascade of events leading to light emission at 520-620 nm—but only when the beads are brought into close proximity (<200 nm) by a specific biological interaction. This proximity requirement eliminates background noise, allowing for highly sensitive detection of a wide range of interaction types, including protein-protein, protein-peptide, and protein-nucleic acid binding, even for very weak or transient complexes that are challenging to study with other techniques.

Fig.1 Schematic illustration of AlphaScreen for detection of non-native IgG. (Senga Y, et al., 2017)
Leveraging state-of-the-art detection platforms, CD BioSciences' AlphaScreen service delivers robust, high-quality data for your most challenging interaction studies. We specialize in developing sensitive and specific assays that provide critical insights for early-stage discovery and screening campaigns.
Measure picomolar-level biomolecular interactions through homogeneous chemiluminescent proximity assays without wash steps.
High-Throughput Screening
Screen 100,000+ compounds daily in miniaturized formats to identify active hits against epigenetic targets.
Target Panel Profiling
Assess compound selectivity across curated panels of bromodomains, methyltransferases, and reader domains in parallel.
Cell Lysate Analysis
Quantify specific binding events in crude biological samples while preserving native protein complexes and modifications.
Supported Sample Types
Diverse Application Scenarios
Q: What types of interactions are best suited for AlphaScreen?
A: AlphaScreen is ideal for studying protein-protein, protein-peptide, and protein-small molecule interactions, especially those that are weak or involve large complexes. Its sensitivity and homogeneous format make it superior to many other techniques for these applications.
Q: How does AlphaScreen compare to TR-FRET?
A: Both are homogeneous, proximity-based assays. AlphaScreen often provides greater signal amplification and sensitivity, making it better for detecting very weak interactions. TR-FRET can offer faster kinetics reading and is less susceptible to certain types of interference.
Q: What are the key advantages of AlphaScreen for high-throughput screening?
A: Its homogeneous "mix-and-measure" format, high sensitivity, robustness, and compatibility with 384-well and 1536-well plates make it an excellent choice for HTS, allowing for the rapid screening of large compound libraries with minimal manual steps.
Our tailored AlphaScreen assays deliver the robust, high-quality data required to confidently characterize complex biomolecular interactions and accelerate your epigenetic research and drug discovery efforts. Contact us today to discuss your specific project requirements, request a detailed quote. We are committed to delivering reliable, actionable data to support your scientific objectives.
Reference
1. Senga Y, Imamura H, Miyafusa T, et al. AlphaScreen-based homogeneous assay using a pair of 25-residue artificial proteins for high-throughput analysis of non-native IgG[J]. Scientific Reports, 2017, 7(1): 12466.
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