Long ncRNAs, circular RNAs, pseudogenes, miRNAs, and messenger RNAs (mRNAs) form a competitive endogenous RNA (ceRNA) network that plays an essential role in cancer, cardiovascular, neurodegenerative, and autoimmune diseases. After years of concentrating on exosomal RNA, Creative Biolabs introduces effective ceRNA microarray services to support our clients' exosomal ceRNA research.
Fig. 1 The regulatory mechanism of exosomal ceRNA.1
Emerging evidence has revealed that exosomal ncRNAs are dysregulated and play important roles in different disorders, including several types of cancer, myocardial infarction, and cholestatic liver diseases. Exosomal ncRNAs may be more functional and integral because they are protected from RNase. So exosomes can be suitable places for RNAs crosstalk and an ideal study model of the ceRNA hypothesis.
The ceRNA theory proposes that RNA could regulate each other by competing for miRNA response elements. The ceRNA theory provides a new perspective on the lncRNA regulatory mechanism. Therefore, systematically constructing the EMs-associated lncRNA-miRNA-mRNAs-ceRNA regulatory networks is crucial and might provide more clues to EM molecular mechanisms.
Fig. 2 Volcano plots and clustering heat map for significantly differential genes response to paclitaxel treatment.2
As an industry-leading exosome research services provider, Creative Biolabs launches exosomal ceRNA microarray services to solve our customers' puzzles in exosomal ceRNA. Compared with the traditional NGS method, our exosomal ceRNA microarray requires fewer amount samples and provides higher efficiency.
If you have problems in exosomal ceRNA research, or you have any questions about Creative Biolabs' services, please feel free to contact us for more information.
A: The microarrays offer high reproducibility and reliability due to stringent quality control measures and optimized protocols.
A: Custom microarray panels can be designed based on specific gene targets or pathways of interest.
A: Exosomal ceRNAs are protected from degradation and reflect the physiological state of cells, making them ideal for biomarker discovery and disease monitoring.
A: The timeline can vary, but it generally takes 8-12 weeks from sample collection to data analysis, depending on sample size and complexity.
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