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Blue-Ribbon Poly A+ RNA and Total RNA
Sure-Race CDNA 5' End Discovery Panels
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Rapid-Screen Arrayed cDNA Library Panels
cDNA Libraries
Molecular Tools
PrecisionShuttle ORF Vector System


OriGene cDNA clones in recent publications
MET Receptor Sequence Variants R970C and T992I Lack Transforming Capacity Cancer Res., Aug 2010; 70: 6233 - 6237 [MET]

Methyl 2-Cyano-3,12-dioxooleana-1,9-dien-28-oate Decreases Specificity Protein Transcription Factors and Inhibits Pancreatic Tumor Growth: Role of MicroRNA-27a Mol. Pharmacol., Aug 2010; 78: 226 - 236 [ZBTB10]

Tumor Lymphangiogenesis and Metastasis to Lymph Nodes Induced by Cancer Cell Expression of Podoplanin Am. J. Pathol., Aug 2010; 177: 1004 - 1016 [PDPN]

AML1 is overexpressed in patients with myeloproliferative neoplasms and mediates JAK2V617F-independent overexpression of NF-E2 Blood, Jul 2010; 116: 254 - 266 [RUNX1]

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SURE-RACE CDNA 5' END DISCOVERY PANELS

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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