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SYBR Green Dye-Based Master Mixes for Real-Time PCR

 

SYBR Green dye-based master mixes are 2x ready-to-use formulations designed for quantitative amplification of DNA targets - including cDNA and genomic DNA - by real-time PCR, using a fluorescent dye that binds double-stranded DNA as it accumulates during amplification. These mixes work with any primer pair without requiring a sequence-specific probe, offering cost-effective flexibility across many targets. 

Academic researchers running gene expression profiling and nucleic acid quantification benefit from the broad compatibility and lower per-assay cost of dye-based detection. Contact customerservice@mbpinc.net to request a quote today!

SYBR/Dye-Based

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2x qPCR Mix SBGR
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2x qPCR Mix, SBGR,  Rox
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2x qPCR Mix, SBGR, Low Rox
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Accuris qMAX Green, with blue tracking dye qPCR Mix
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Accuris qMAX Probe qPCR Mix
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AzuraQuant™ Green 1-Step qPCR Mix HiRox
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USD114.00 - USD3,923.50
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AzuraQuant™ Green 1-Step qPCR Mix LoRox
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AzuraQuant™ Green Fast qPCR Mix HiRox
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AzuraQuant™ Green Fast qPCR Mix LoRox
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USD86.45 - USD2,600.15
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AzuraView™ GreenFast qPCR Blue Mix HR
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AzuraView™ GreenFast qPCR Blue Mix LR
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What is a SYBR Green Dye-Based Master Mix?


A SYBR Green dye-based master mix is a 2x, ready-to-use formulation designed for dye-based, quantitative amplification of DNA targets, including cDNA and genomic DNA, by real-time PCR. SYBR Green dye binds to double-stranded DNA formed during amplification, and the resulting fluorescence increases proportionally to the quantity of double-stranded product, providing a real-time readout of amplification progress. Choose a SYBR Green dye-based master mix for cost-effective, flexible quantification across any primer pair and target combination, especially when running many different assays without the overhead of probe design.

 

What you will find:

 

  • SYBR Green dye-based qPCR master mixes for real-time quantification of DNA and cDNA targets across a wide range of research applications.
  • Fast qPCR formulations with HiROX and LoROX options to support compatibility with different real-time PCR instrument platforms.
  • Blue tracking dye master mixes, including AzuraView™ GreenFast and Accuris qMAX Green formats, for improved reaction setup visibility.
  • One-step SYBR Green RT-qPCR mixes that combine reverse transcription and real-time PCR in a single tube for RNA quantification workflows.
  • Ready-to-use 2x master mixes formulated for reproducible qPCR setup while reducing pipetting steps and workflow complexity.


How to Choose a SYBR Green Dye-Based Master Mix


Dynamic Range and Sensitivity
Look for master mixes offering a wide linear dynamic range -- some formulations provide precise measurement across approximately six logs of dynamic range, enabling accurate detection across both low- and high-concentration samples in the same assay design.

Primer Melting Temperature Flexibility
SYBR Green master mixes are commonly formulated to provide flexibility for primers with melting temperatures (Tm) in the range of approximately 55-65 °C, reducing the need for extensive primer-specific optimisation when bringing new assays online.

Bench-Top Stability
Dual hot-start mechanisms in some SYBR Green master mixes provide extended bench-top stability -- up to 72 hours at room temperature in the dark in some formulations -- with single melt curves confirmed at both initial and post-incubation time points, supporting automated and batched workflows.

Carryover Contamination Prevention
Formulations that include uracil-DNA glycosylase (UDG) and dUTP help ensure leftover DNA residue from previous reactions is not re-amplified in subsequent experiments, a useful feature for high-throughput repeat assays.

Instrument and Workflow Compatibility
Broad instrument compatibility - including standard and fast cycling modes -- and compatibility with a variety of reverse transcriptase enzymes (for RT-qPCR workflows using a separately generated cDNA) widen the range of platforms a single master mix can support.


Specifications Context


SYBR Green dye is a fluorescent double-stranded DNA-binding dye that tracks amplification progress in real-time PCR: as the reaction proceeds, the dye binds newly synthesised dsDNA at each extension step, and the resulting fluorescence increase is proportional to product quantity. Because SYBR Green is not PCR-inhibitory and works with any primer-template combination, it provides accurate, reproducible results with high sensitivity across a broad dynamic range and gives consistent results across different real-time PCR platforms - one reason dye-based chemistry remains cost-effective compared to probe-based systems, which require a different labelled probe for each target sequence. SYBR Green master mixes are typically stored at −20 °C to −30 °C and protected from light; lot-specific CoAs are available on request.

 

Contact the expert team at MBP today and get high-yield SYBR/Dye-Based real-time PCR reagents for your lab.

FAQ

SYBR Green dye binds to double-stranded DNA formed during amplification. As the reaction proceeds, the dye binds newly synthesized dsDNA at each extension step, and the resulting fluorescence increase is proportional to the quantity of double-stranded product, providing a real-time readout of amplification progress.
Some SYBR Green master mix formulations provide precise measurement across approximately six logs of dynamic range, enabling accurate detection of both low- and high-concentration samples within the same assay design.
SYBR Green master mixes are commonly formulated to provide flexibility for primers with melting temperatures in the range of approximately 55-65 degrees Celsius, reducing the need for extensive primer-specific optimisation when bringing new assays online.
Some SYBR Green master mixes with a dual hot-start mechanism offer extended bench-top stability, with reproducibility demonstrated up to 72 hours at room temperature in the dark in certain formulations, supporting automated and batched workflows.
Uracil-DNA glycosylase (UDG) and dUTP, included in some SYBR Green master mix formulations, help ensure leftover DNA residue from previous reactions is not re-amplified in subsequent experiments. This carryover contamination control is useful for high-throughput repeat assays.
Yes. SYBR Green is not PCR-inhibitory and binds any double-stranded DNA non-specifically, so it works with any combination of primers and template. This contrasts with most probe-based systems, which require a different labelled probe for each target sequence.
Many SYBR Green master mixes are designed for broad compatibility with a variety of reverse transcriptase enzymes, relevant for RT-qPCR workflows using a separately generated cDNA template in a two-step approach.
SYBR Green master mixes are typically stored at -20 to -30 degrees Celsius and protected from light. Lot-specific certificates of analysis documenting performance and quality control testing are available on request from MBP.
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