miProfile™ miRNome miRNA qPCR Arrays

For high-throughput profiling of miRNA whole genome expression

*Promotions are valid in the US & Canada only. For international customers, please contact your local distributors. Promotion ends February 28, 2025. Discounts are not valid on previous purchases and cannot be combined with additional discounts.
Introduction
The miProfile human miRNome miRNA qPCR arrays are a set of nineteen 96-well plates covering 1,700 of best characterized and annotated miRNAs based on miRBase V18. Each 96-well plate contains up to 84 pairs of PCR primers (forward: miRNA-specific primer; reverse: universal primer) and 12 wells of different types of controls, which are used to monitor the efficiency of the entire experimental process – from reverse transcription to qPCR reaction.
Each miRNA-specific primer used in the qPCR arrays has been experimentally validated to yield a single dissociation curve peak and to generate a single amplification of the correct size for the targeted miRNA. A cDNA pool, containing reverse transcript products of 10 different tissue total RNAs, was used as the qPCR validation template.
Using a universal real-time PCR condition, one can easily profile and analyze the miRNA expression in a high-throughput fashion. The All-in-One™ miRNA First-Strand cDNA Synthesis Kits and qPCR Mix Kits are the recommended  and supported RT-PCR reagents for use with the miProfile miRNA qPCR arrays. These reagents have been optimized to produce high sensitivity, efficiency, and specificity.
To help best distinguish single-nucleotide mismatched miRNAs, 61 single-nucleotide mismatched miRNAs from the human miRNome are further grouped together on one 96-well plate. The miProfile human single-nucleotide mismatch miRNA qPCR array is available as stand-alone products for users who want to study these miRNAs using specific PCR conditions.
To view other miProfile miRNA qPCR arrays, click below:
 

Key Advantages

Validated miRNA primers
  • Each miRNA primer is designed using a proprietary algorithm and experimentally validated
Robust performance
  • Sensitive – Detect miRNA from as little as 10 pg of small RNA or 20 pg of total RNA
  • Specific – Be able to distinguish miRNAs with single nucleotide mismatches. Each primer set has been experimental validated for specific amplification
  • Broad linearity– Allow miRNA at varieties of expression level to be detected simultaneously
  • Reproducible – High reproducibility (R2>0.99) for inter-array and intra-array replicates
Largest coverage
  • More than 1,700 of best characterized and annotated miRNAs are covered based on miRBase V18