Consistent and reliable reagents for diagnostic testing, development, and biopharma manufacturing quality control, and clinical trial assay development
Molecular diagnostics testing, assay development, and biopharma processes require real-time PCR (qPCR) reagents with the highest level of consistency and reliability. With stringent cGMP manufacturing, excellent performance, and compliance documentation support, Applied Biosystems TaqPath general purpose reagents are designed to deliver confidence and reliability for even your most demanding applications. TaqPath master mixes are labeled “For Laboratory Use” and optimized for exceptional lot-to-lot consistency.
For master mixes that support research workflows, see our TaqMan qPCR master mixes.
TaqPath master mixes are optimized to simplify your IVD assay development and regulatory submissions, clinical trials QC, etc. Supporting compliance package documents are available on the product pages accessed below.
Which TaqPath master mix is right for your application?
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Recommended applications | Pathogen detection Gene expression | Microbial detection | SNP genotyping Copy number variation | Gene expression MicroRNA analysis |
Target | RNA | DNA | gDNA | cDNA |
Concentration | 4X | 2X | 2X | 2X |
Multiplexing and passive reference dye | Available in two versions: | Available in two versions: | Available in two versions: With ROX (up to 3 targets) | With ROX (up to 3 targets) |
Reverse transcriptase | Thermostable MMLV RT included | N/A | N/A | Purchase RT separately and use before qPCR |
Cycling mode/run time | Standard: ~110 min Fast: ~60 min | Standard: ~120 min Fast: ~50 min | Standard: ~120 min Fast: ~50 min | Standard: ~50 min Fast: ~40 min |
Carryover contamination | UNG compatible (UNG not included) | With UNG | With UNG | With UNG |
Assay recommendation | ||||
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TaqPath master mixes are general purpose reagents labeled ‘For Laboratory Use’ and manufactured in an ISO 13485-certified and FDA-registered facility that adheres to cGMP principles. Every lot is functionally tested to help ensure lot-to-lot reproducibility for Ct consistency across a wide dynamic range.
For additional workflow components that support biopharma applications, see our QualTrak qPCR biopharma ecosystem.
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