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Blue-Ribbon Poly A+ RNA and Total RNA
Rapid-Screen Arrayed cDNA Library Panels
cDNA Libraries
Molecular Tools
PrecisionShuttle ORF Vector System

OriGene cDNA clones in recent publications
Tumor cell-secreted angiogenin induces angiogenic activity of endothelial cells by suppressing miR-542-3p Cancer Lett. Nov 2015 [POU2F1]

OP9-Lhx2 stromal cells facilitate derivation of hematopoietic progenitors both in vitro and in vivo Stem Cell Research Sep 2015 [LHX2]

The presence of Estrogen Receptor ß modulates the response of breast cancer cells to therapeutic agents Int. J. Biochem. Cell Biol. Sep 2015 [ESR2]

A novel GLP-1 receptor interacting protein ATP6ap2 regulates insulin secretion in pancreatic beta cells J. Biol. Chem. Aug 2015 [ATP6AP2]

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Traditional cDNA libraries frequently yield clones which are incomplete and where sequences representing mRNA 5' ends are missing. RACE technology, a PCR-based approach for rapid amplification of cDNA ends, has been particularly useful for completing the missing portions of cDNA clones and yielding full-length sequences of expressed gene regions.

To expand the utility of the RACE technology, OriGene has developed Sure-RACE cDNA 5 End Discovery Panels - PCR-ready RACE panel that allow simultaneous 5' end analysis of transcripts from 24 individual human tissues or 24 mouse tissues and developmental stages. Sure-RACE cDNA 5 End Discovery Panels contain double-stranded cDNAs that have been arrayed in multi-well plates.

  • Broad spectrum of tissues: scan 24 individual human or mouse tissues
  • High sensitivity: detect rare transcripts
  • Simultaneous analysis of alternatively spliced transcripts and alternate RNA start-sites

Sure-RACE Discovery Panels are designed with the recognition that an increasing number of genes have been identified that utilize alternate RNA start-sites resulting from tissue-specific or developmental stage-specific transcriptional promoters. In addition, an increasing number of genes have also been found to utilize alternate 5 exons, sometimes resulting in protein products with different N-terminal amino acid sequences.

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