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miRCURY LNA miRNA Custom Bulk Plate

Customer-configurable SYBR® Green-based miRNA qPCR Assays in convenient plate format


  • Customer-configurable plate containing miRCURY PCR Assays for 200 reactions per well
  • Add predesiged miRCURY PCR Assays or custom designed miRCURY PCR Assays
  • Easy ordering via the GeneGlobe plate designer

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miRCURY LNA miRNA Custom Bulk Plate (200)

Cat. No. / ID: 339319

miRCURY LNA miRNA PCR Assays in 96-well format; plate configuration specified by the customer; 200 reactions per well; for SYBR® Green-based detection
miRCURY LNA miRNA Custom Bulk Plate are intended for molecular biology applications. These products are not intended for the diagnosis, prevention, or treatment of a disease.

✓ 24/7 automatic processing of online orders

✓ Knowledgeable and professional Product & Technical Support

✓ Fast and reliable (re)-ordering

Product Details

miRCURY LNA miRNA Custom Bulk Plates are 96-well plates containing individual miRCURY LNA miRNA PCR Assays according to your particular requirements. Both forward and reverse PCR amplification primers are miRNA-specific and are optimized with LNA technology, enabling extremely sensitive and specific miRNA quantification with the miRCURY LNA miRNA PCR System. Each well contains enough primer set for 200 reactions.

Need a quote for your research project or would you like to discuss your project with our specialist team? Just contact us!


The design process
The miRCURY LNA miRNA Custom PCR Assay design tool lets you easily design highly sensitive and specific LNA-enhanced PCR primer sets for any miRNA not available as a predesigned product. The advanced algorithm evaluates approximately 3,000 primer pair designs based on more than 60 different criteria to find LNA optimal primer sets for your miRNA within a few minutes. The tool has been designed for miRNAs but can also be used for other small RNAs 14–27 nucleotides in length.

The design criteria include:
  • Optimization of melting temperatures by varying the LNA distribution of the primers to ensure high amplification efficiency and specificity.
  • Calculations and adjustments of self-hybridization and cross-hybridization scores for efficient PCR reactions.
  • Adjustments to avoid potential primer–dimer formation in the PCR reaction.
  • Intelligent positioning of LNA bases in the primers based on our vast knowledge of LNA oligonucleotide design.
  • miRBase searches to identify potential miRNAs with high sequence similarity. This ensures that the primer sets are highly specific for the small RNA for which they were designed.

Unmatched sensitivity
The exceptional sensitivity of miRCURY LNA miRNA PCR Assays is achieved by combining universal reverse transcription with LNA-enhanced and Tm-normalized primers. This combination enables accurate and reliable quantification of individual miRNAs from as little as 1 pg of total RNA input in the initial first-strand cDNA synthesis (see figure  Accurate quantitation from down to 1 pg total RNA starting material).

Compared with other miRNA real-time PCR systems that use either stem-loop or standard DNA primers, the LNA-enhanced primers offer significantly increased sensitivity, especially for AT-rich miRNAs (see figure  LNA-enhanced primers result in greatly increased sensitivity compared to DNA primers).

The low sample requirements also enable miRNA quantitation using total RNA purified from difficult samples such as LCM samples and serum/plasma (see figures  Detection of differential expression of miRNAs in LCM specimens from FFPE tissue sections and  Differences in miRNA expression between serum samples).

Fully validated and optimized
All wet-lab validated miRCURY LNA miRNA PCR Assays have been optimized to be as sensitive as possible. Over 80% of assays detect at least 5 miRNA copies in the PCR reaction (see figure  Serial dilution of hsa-miR-181a). The primer sets have also been validated for specific amplification of the target and for minimal background signal (see figure  Specific and sensitive amplification of miRNA).

The only platform with perfect specificity
The miRCURY LNA miRNA PCR Assays are the only miRNA quantification platform with absolute specificity (see the miRQC study published in Nature Methods) and out-performed another probe-based miRNA qPCR platform in specificity tests (see figure Specificity test with probe-based miRNA qPCR system). Perfect specificity eliminates false positives and ensures only robust and reliable miRNA signals.

Superior discrimination
The incorporation of LNA in both the forward and reverse PCR amplification primers makes it possible to design assays that can distinguish between miRNA sequences that differ by only one nucleotide (see figure  Single-nucleotide discrimination). In addition, the assays can discriminate between mature miRNA sequences and precursor miRNA.

Fast, easy and reproducible
The easy-to-follow, 3-hour protocol saves you both time and effort in the laboratory. By using the same RT reaction as the template in all subsequent PCR reactions, the procedure is greatly simplified compared with systems that require miRNA-specific first-strand synthesis. The number of pipetting steps is reduced to a minimum, and technical variation is minimized. This makes it possible to achieve extremely high reproducibility from day-to-day and even site-to-site.

miRCURY LNA miRNA PCR Assays have been optimized for use with the miRCURY LNA RT Kit and the miRCURY LNA SYBR Green PCR Kit. Use of other reagents will affect the quality of the results.
See figures


A unique system for miRNA profiling
miRCURY LNA miRNA PCR Assays offer the best combination of performance and ease-of-use available on the miRNA real-time PCR market by combining universal RT with LNA PCR amplification (see figure  Schematic outline of the miRCURY LNA miRNA PCR System). Universal RT makes it possible to use one first-strand cDNA synthesis reaction as the template for multiple miRNA real-time PCR assays. This saves precious samples, reduces technical variation and saves time in the laboratory. Plus, both the forward and reverse PCR amplification primers are miRNA specific and optimized with LNA. This provides 1) exceptional sensitivity and extremely low background, enabling accurate quantitation of very low miRNA levels and 2) highly specific assays that allow discrimination between closely related miRNA sequences.

Over 20,000 assays are available covering all organisms in miRBase 20. Over 1,400 assays are fully wet-lab validated for sensitivity, specificity, efficiency and background on both synthetic as well as different biological samples. The remaining assays are in silico-validated using a comprehensive design algorithm that ensures high-quality, species-specific, LNA-enhanced assays with optimal sensitivity and specificity within each organism. This means that several different assays may target the same sequence. Ultimately, the assay for each species is selected based on the genetic background of the organism. If you are working with novel miRNAs, such as from an NGS experiment, custom-designed LNA miRNA primer sets for any miRNA are also available.
See figures


The miRCURY LNA miRNA PCR Assay system is an miRNA-specific, LNA-based system designed for sensitive and accurate detection of miRNA by quantitative real-time PCR using SYBR Green. The first step of the procedure is universal reverse transcription, followed by real-time PCR amplification with LNA-enhanced primers (see figure miRCURY LNA miRNA PCR System at a glance).


miRCURY LNA miRNA PCR Assays are used as part of the miRCURY LNA miRNA PCR System for:
  • Mature miRNA quantification
  • snoRNA detection

Supporting data and figures


Safety Data Sheets (1)
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