qMAXSen™ Green qPCR MasterMix (Low ROX™)


Starting at $208.68

Product Name Qty
qMAXSen™ Green qPCR MasterMix (Low ROX™)
250 rxn


qMAXSen™ Green qPCR MasterMix 2x (Low ROX™) offers exceptional sensitivity, specificity & performance for real-time PCR using a green fluorescent dye. Supplied as stabilized 2x reaction mixture, qMAXSen is a convenient and easy, ready-to-use premix to perform qPCR using an analog fluorescent dye to SYBR® Green. The optimized MasterMix includes all the components required for running PCR reactions, except PCR primers and template.

Available with or without the option of ROX™ as the internal passive reference dye. ROX™ provides an internal reference to which the reporter-dye signal can be normalized during data analysis. See related products: Q-2437 (w/o ROX™) and Q-2441 (High ROX™).


Advantages & Features

 Exceptional Sensitivity: for increased limit of detection
 High Specificity: due its Hot-Start Antibody technology
 Safe: minimize contamination risk using optimized protocol that reduces pipetting steps
 Great signal-to-noise ratio
 Versatile: compatible with most used real-time PCR instruments
 Accurate quantification of a variety of gene targets



• Detection and quantification of DNA and cDNA targets
• Gene expression
• Low copy detection
• High throughput applications
• qPCR for post reverse transcription step



 Taq Source: E. coli strain with cloned Taq DNA Polymerase gene from Thermus aquaticus.
• Contains materials for 250 reactions (2 x 1.25 mL): includes 2x mixture of dNTPs, HotStart DNA Polymerase, Mg2+, fluorescent detection dye, reference dye & proprietary buffer components



*Developed and manufactured by Canvax Biotechnology, S.L under contractual agreement for AG Scientific, Inc.

More Information
Storage Temp
-20 °C upon receipt. ROX™ reference dye is sensitive to exposure to light. Avoid repeated freezing and thawing.
qPCR DNA and cDNA target detection and quantification, gene expression, low copy detection, high throughput applications, qPCR for reverse transcription
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