Webinars Archives

Arraystar m6A Single Nucleotide Arrays uses methyl-sensitive MazF RNase to precisely locate the m6A site and microarray for ultrasensitive detection.

The webinar covers:
1) The roles of m6A sites in human cancers and diseases;
2) How to best profile and study m6A sites.​

tRNAs are not only the fundamental component in protein translation, but also new found regulatory molecules. Watch and learn more about tRNAs, the rising star of wobble gene regulators!

Learn the latest publications about the limitations of RNA-seq for LncRNA profiling, and what’s new our recently updated LncRNA microarrays can offer.

Current transcriptome-wide RNA modification profiling methods deal mostly with mapping the modification sites but are unable to achieve modification stoichiometry. The lack of such quantitative information has been a major concern for scientists. This video presents how Arraystar Epitranscriptomic two-color channel microarrays quantify the percentage of RNA that is modified for each transcript isoform.

Circular RNAs (circRNA) are resistant to exonuclease degradation and some can be present at abundant yet cell type specific levels. Many circRNAs harbor multiple microRNA binding sites to function as microRNA sponges in gene regulation. Their unique properties poses special profiling challenges. We will discuss the best practical circRNA profiling solutions and share the success stories.

Super-enhancers are top ranking master gene regulators that program the cell lineages, types, identities, and diseases. Super-enhancer lncRNAs (SE-lncRNA) transcribed from the super-enhancers activate the target coding genes by multiple mechanisms. Arraystar SE-lncRNA microarrays simultaneously profile SE-lncRNAs and their target genes, with high sensitivity, unambiguous isoform detection, comprehensive annotations and transcript-specific level accuracy.