Arraystar piRNA Arrays are designed to profile tens of thousands of piRNAs at high specificity and sensitivity, for the study of piRNA biology, molecular functions, and biomarker applications. We offer the complete piRNA array service, from sample to publishable data!
• Comprehensive collection and reliable selection of piRNA sequences.
• 60-mer oligonucleotide probes using duplex design to achieve high specificity.
• Duplicated probes for most of the piRNAs.
Piwi-interacting RNAs (piRNAs) are the largest class of single stranded, small non-coding RNAs of about 26-32 nucleotides in length. piRNAs interact with the Piwi (P-element Induced Wimpy Testis) subfamily of Argonaute proteins. The Piwi subfamily comprises Piwi, Aubergine and AGO3 in flies, MILI, MIWI and MIWI2 in mice, and HILI, HIWI1, HIWI2 and HIWI3 in humans. Individual piRNAs are very diverse and are poorly conserved even between closely related species. In contrast to several hundred microRNA species, tens of thousands of unique piRNA sequences are known in human, mouse and rat. piRNAs are strikingly different from microRNAs in their length, expression pattern, genomic organization and biogenesis.
Arraystar's scientists have developed piRNA arrays for human, mouse and rat species to evaluate the global expression of piRNAs. The piRNA sequences from all three organisms are downloaded from the NCBI database, and mapped to the genome sequences (HG19, MM9 and RN4) using UCSC Blat. Antisense 60-mer oligonucleotide probes are designed using a duplex method. Our piRNA arrays sensitively and accurately profile the expression of piRNAs.
||Arraystar Human piRNA Array
||Arraystar Mouse piRNA Array
||Arraystar Rat piRNA Array
|Number of piRNAs
||Ligation of Cy3 label with dephosphorylated RNA by T4 RNA ligase
||4 * 44K
||4 * 44K
||4 * 44K
Arraystar scientists have extensive experience with microarray data processing and analysis. piRNA array raw data points are extracted, QC flagged, and quantile normalized. The gene expression values and annotations are compiled. Differentially expressed piRNAs are identified by the fold change and statistical significance.
Figure. piRNA array data analyses and graphic display items are included in the standard analysis package.
Please refer to Sample Submission for details on how to get your project started.
• RNA isolation (Optional)
• RNA QC
• Target reparation by labeling with Cy3
• Array hybridization, washing, and scanning
• Data extraction, analysis and summarization
The piRNA CHAPIR regulates cardiac hypertrophy by controlling METTL3-dependent N 6-methyladenosine methylation of Parp10 mRNA. Gao X Q, et al. Nature Cell Biology, 2020
PIWIL3/OIP5-AS1/miR-367-3p/CEBPA feedback loop regulates the biological behavior of glioma cells. Liu X, et al. Theranostics, 2018
RASSF1C modulation of Piwi-interacting RNAs (piRNAs) in lung cancer.YG Amaar, et al.Cancer Research, 2015
Roles of piRNAs in microcystin-leucine-arginine (MC-LR) induced reproductive toxicity in testis on male offspring. Zhang L, et al. Food and Chemical Toxicology, 2017
Piwi-interacting RNAs as novel prognostic markers in clear cell renal cell carcinomas. J Busch, et al. J Exp Clin Cancer Res, 2015
Altered Expression of PIWI RNA in the Rat Brain After Transient Focal Ischemia. Ashutosh Dharap, Venkata Prasuja Nakka and Raghu Vemuganti. STROKEAHA, 2010.