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Multi-platform Compatibility: Compatible with RPA, LAMP, and CRISPR SHERLOCK workflows.
NUCLEIC ACID TEST STRIPS
Based on lateral flow technology, EZassay enables rapid visual readout of RPA, LAMP, and CRISPR-based detection results. Multiple formats including single-target, dual-target, line-appearance, and line-disappearance detection are available for molecular diagnostic development.
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Multi-platform Compatibility: Compatible with RPA, LAMP, and CRISPR SHERLOCK workflows.
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Rapid Visual Readout: Results available within 5–15 minutes without specialized equipment.
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Flexible Detection Formats: Supports single-target, dual-target, and multiple CRISPR readout formats.
Based on lateral flow technology, EZassay nucleic acid test strips provide rapid and reliable visual readout solutions for RPA, LAMP, and CRISPR-based nucleic acid detection platforms. With flexible labeling strategies and multiple detection formats, EZassay enables convenient applications from laboratory research to field-based rapid testing.
Multiple Amplification Compatibility: Compatible with RPA, LAMP, and other isothermal amplification technologies for rapid visual readout.
Flexible CRISPR Detection Formats: Supports Cas12, Cas13, and other CRISPR-based nucleic acid detection workflows.
Instrument-Free Visual Readout: Direct visual interpretation without fluorescence equipment, enabling rapid point-of-care testing.
Closed-Tube Workflow for Contamination Prevention: Customized consumables minimize opening steps after amplification and reduce aerosol contamination risks.
Based on lateral flow technology, nucleic acid test strips generate visual signals by specifically recognizing labeled amplification products or CRISPR-generated reporter signals. Different detection formats produce distinct changes at the test line (T line) and control line (C line), enabling rapid result interpretation.
FAM/FITC + Biotin dual-labeled amplification products with T/C line readout
Operating Conditions
Dilute 10 µL amplicon 10-20 fold with Diluent Buffer; load 70 µL and read within 5 minutes.
Result Interpretation

T1/T2 dual test lines for simultaneous dual-target detection
Operating Conditions
Mix 5 µL amplicon with 100 µL Diluent Buffer; load 80 µL and read within 15 minutes.
Result Interpretation

T-line appearance upon CRISPR activation
Operating Conditions
Mix 10 µL CRISPR-Cas reaction product with 40 µL ddH₂O. Insert the strip, keep liquid below the MAX line, and read after 5-10 minutes.
Result Interpretation

Target-triggered Cas activation cleaves the reporter, resulting in T-line disappearance
Operating Conditions
Mix 2 µL amplicon with 78 µL Diluent Buffer; load 70 µL and read within 5 minutes.
Result Interpretation

| Product Name | Compatible Platform | Recommended Application | Key Features |
|---|---|---|---|
| Nucleic Acid Test Strip | RPA/LAMP | Single–Target Detection | Simple workflow for rapid visual detection of amplification products |
| Dual–Test Line Nucleic Acid Test Strip | RPA/LAMP | Dual–Target Detection | Enables simultaneous detection of two targets, increasing detection capacity and application flexibility |
| CRISPR SHERLOCK Test Strip (Direct Format) | Cas12a/Cas13a | Direct Visual CRISPR Detection | Generates visual signals upon CRISPR activation, providing intuitive readout for rapid assay development |
| CRISPR SHERLOCK Line–Disappearance Test Strip (Indirect Format) | Cas12a/Cas13a | Direct Visual CRISPR Detection | Positive results are determined by T–line disappearance, with sufficient reaction time to improve detection stability |
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Select the appropriate nucleic acid test strip based on the detection platform, labeling strategy, and result readout format.