MicroRNAs are single-stranded, 19- to 25-nucleotide RNAs that regulate gene expression post-transcriptionally by binding to the 3’ untranslated regions (UTRs) of target mRNAs, inhibiting their translation. The high relative stability of miRNA in biofluids (e.g., plasma, serum, urine, saliva, etc.) and the ability of miRNA expression profiles to accurately classify discrete tissue types and disease states have positioned miRNA quantification as a promising new tool for a wide range of biomarker discoveries. MicroRNAs are gaining popularity in emerging applications such as early detection of cancer, cardiovascular diseases, and simultaneous detection of miRNA and mRNA from the same samples for pathway analysis, etc.
This webinar focuses on pancreatic cancer research using the simultaneous measurement and analysis of mRNA and miRNA in the same sample.
Get answers to the most frequently asked qPCR questions with our library of quick and easy educational videos covering a variety of topics including experiment setup, best practices, and guidance on products and technologies.
This article covers microRNA biogenesis and regulation, cellular function and disease, target prediction and validation.
A brief explanation and illustration of how the TaqMan chemistry works in the various applications of gene expression, genotyping, copy number variation, microRNA, mutation detection, and protein quantification.
A video that discusses comparison of small RNA sequencing and RT-qPCR profiles from nevus and melanoma FFPE samples.
A short video that explains the purpose of normalization and endogenous controls, exogenous controls, and mean expression methods.
This application note describes the workflow, reagents, and tools for recovery and analysis of circulating miRNAs from blood samples.
Discusses the isolation and detection of miRNAs from formalin- or paraformalin-fixed, paraffin-embedded (FFPE) samples and demonstrates the accurate and robust measurement of miRNA expression from comparable snap-frozen samples.
Learn more about Ct (threshold cycle), the intersection between an amplification curve and a threshold line. It is a relative measure of the concentration of target in the PCR reaction.
This whitepaper highlights the TaqMan probe based performance for detecting low-abundance miRNAs, measurement of small fold-changes in serum, and single-base discrimination of related miRNAs.
Discussion of a workflow to identify the two or three most stable miRNAs in a set of samples and use them as endogenous controls to normalize miRNA expression in qPCR studies.
Learn how genetic analysis techniques, including sequencing, NGS, and quantitative and digital PCR, are being used by researchers to advance knowledge and innovations in challenging disease and research questions.
This video discusses the basic concepts of miRNAs and miRNA research.
For Research Use Only. Not for use in diagnostic procedures.