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Mouse LncRNA Microarray V2.0

 

The Arraystar Mouse LncRNA Microarray V2.0 is designed for the global profiling of mouse LncRNAs and protein-coding transcripts together in parallel. Each transcript is represented by a specific exon or splice junction probe that can identify individual transcripts reliably and accurately. This makes it possible to look beyond the genes and study more subtle and relevant RNA expression changes.

Highlights:
•   Comprehensive and Reliable Array Content: Detects LncRNAs compiled from the most updated transcriptome databases and many other relative literatures
•   Most Extensive and Updated Coverage Available: Covers 31,423 LncRNAs and 25,376 protein-coding transcripts
•   Specific Exon or Splice Junction Probes: Enables the identification of individual transcripts reliably and accurately
•  Efficient and Robust Labeling System: Makes it possible to create Cy3 or Cy5 labeled antisense RNA with low input or degraded RNA samples
•  Systematic LncRNA Classification: Helps to identify the putative functional relationship between LncRNAs and their associated protein-coding genes
 
Data Sources
 
Specifications:
Total Number of Distinct Probes
59,709
Probe Length
60 nt
Probe Selection Region
Specific exon or splice junction probes along the entire length of the transcript
Probe Specificity
Transcript specific
Labeling Method
Utilizing a random priming method to generate Cy3 or Cy5 labeled antisense RNAs along the entire length of the transcript without 3' bias
Protein Coding Transcripts (mRNAs)
25,376
LncRNAs
31,423
LncRNA Sources
LncRNA collections are based on:
Databases: NCBI Refseq, UCSC Known Gene 4, Ensembl 37.61, Fantom3, RNAdb 2.0 and NRED;
Literatures: LincRNAs[1], T-UCRs[2], Evolutionary constrained LncRNAs[3], Evolutionary conserved LncRNAs[4], and UaRNAs [5]
mRNA Sources
mRNA collection is based on:
NCBI Refseq
Array Format
8 x 60K

References:
1.      Khalil, A.M., et al., Many human large intergenic noncoding RNAs associate with chromatin-modifying complexes and affect gene expression. Proc Natl Acad Sci U S A, 2009. 106(28): p. 11667-72.
2.      Calin, G.A., et al., Ultraconserved regions encoding ncRNAs are altered in human leukemias and carcinomas. Cancer Cell, 2007. 12(3): p. 215-29.
3.      Ponjavic, J., et al., Genomic and transcriptional co-localization of protein-coding and long non-coding RNA pairs in the developing brain. PLoS Genet, 2009. 5(8): p. e1000617.
4.      Willingham, A.T., et al., A strategy for probing the function of noncoding RNAs finds a repressor of NFAT. Science, 2005. 309(5740): p. 1570-3.
5.      Mercer, T.R., et al., Expression of distinct RNAs from 3' untranslated regions. Nucleic Acids Res, 2010.
 

 

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