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High-GC Multiplex Probe qPCR Mix with UDG

Cat.No: NATR-HMM-0197 Datasheet

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Product Details Related Products
Product Name High-GC Multiplex Probe qPCR Mix with UDG
Catalog No. NATR-HMM-0197
Description A multiplex probe qPCR mix optimized for GC-rich DNA templates, combining hot-start amplification, inhibitor tolerance and dUTP/UDG carryover control.
Intended Use Gene-expression analysis; multiplex DNA quantification; amplification of GC-rich targets.
Principle / Technology A hot-start DNA polymerase and GC-tolerant buffer promote efficient probe amplification of GC-rich templates, while dUTP/UDG reduces carryover contamination.
Detection Method Multiplex fluorescent probe-based real-time PCR.
Sample Type DNA templates, particularly GC-rich targets and samples containing common amplification inhibitors.
Performance Range / Specifications 100 or 500 reactions; supports fast cycling, multiplex detection and robust amplification of high-GC templates.
Specificity Optimized hot-start chemistry supports specific amplification and well-defined fluorescence curves.
Reaction Conditions / Protocol Add primers, probes and DNA template to the 2× mix and run a compatible standard or fast multiplex qPCR program.
Components / Formulation 2× high-GC multiplex probe qPCR mix containing hot-start DNA polymerase, optimized GC-tolerant buffer, dUTP/UDG system and passive-reference dye formulation.
Storage Conditions Store at −30 to −15°C.
Package Specifications 100 reactions; 500 reactions.
Product Form 2× high-GC multiplex probe qPCR mix with UDG.
Key Features High-GC template compatibility; high specificity; inhibitor tolerance; fast-program support; carryover contamination control.
Shipping Conditions Ship at or below 0°C.
Compatibility Passive-reference formulation 1 is suitable for instruments such as ABI 7900HT, 7300 and StepOnePlus; formulation 2 is suitable for ABI 7500, 7500 Fast and Stratagene Mx3000P; no passive reference is required for compatible Roche and Bio-Rad instruments.

For research use only, not for clinical use.

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