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Rapid detection of mycoplasma contamination for routine laboratory monitoring.
Mycoplasma
Mycoplasma Detection, Elimination & Prevention
Rapid mycoplasma testing solutions based on nucleic acid amplification technology, covering over 99% of common mycoplasma species. Designed to support a complete workflow from detection and elimination to contamination prevention.
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Integrated solutions for mycoplasma detection, elimination, and prevention.
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No complex instrumentation required and compatible with standard laboratory workflows.
Product Overview
Mycoplasma contamination is a common challenge in cell culture.
- Because mycoplasma lack a cell wall and are difficult to detect using conventional microscopy, contamination can persist unnoticed and affect experimental outcomes.
- Mycoplasma can alter cell metabolism, growth, and reproducibility, creating risks for research and biomanufacturing.
- A comprehensive strategy combining detection, elimination, and prevention helps maintain culture quality and reduce contamination risk.
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qPCR-Based Detection
A well-established method for mycoplasma testing, widely used in biopharmaceutical manufacturing, cell culture, and quality control applications.
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LAMP Lateral-Flow Assay
No qPCR instrument required. Delivers results highly consistent with the pharmacopoeia culture method. Featuring a contamination-controlled workflow and simple operation, it is ideal for both on-site and routine laboratory testing.
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LAMP Colorimetric Assay
Results are interpreted directly through a color change, providing a simple and intuitive solution for rapid yes/no mycoplasma screening.
Testing Workflow
A streamlined workflow from sample preparation to result interpretation, designed for fast and reliable mycoplasma testing.
- Simple: no specialized equipment required
- Fast: results in under 1 hour with minimal hands-on time
- Sensitive: detects contamination levels as low as 10-100 CFU/ml.
- Clear: Easy visual interpretation using a lateral-flow strip
STEP 1
Heat the cell culture supernatant at 99°C for 3 minutes.
STEP 2
Add the reaction buffer, followed by the sample.
STEP 3
Incubate at 39°C for 20–30 minutes.
STEP 4
Insert the lateral-flow strip into the reaction mixture and read the results within 10 minutes.
1-on-1 Expert Support
Get personalized guidance from our technical experts to help solve complex research challenges, so you can stay focused on your science.
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Chat with us
Send us an email: info@ezassay.com
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Call us
Call our team Mon–Fri from 8am to 5pm.
+86 19925271988