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OriGene cDNA clones in recent publications
Early Changes in Cytochrome P450s and Their Associated Arachidonic Acid Metabolites Play a Crucial Role in the Initiation of Cardiac Hypertrophy Induced by Isoproterenol Drug Metab. Dispos. Aug 2015 [CYP2J2]

Theaflavin-3,3'-digallate, a black tea polyphenol, stimulates lipolysis associated with the induction of mitochondrial uncoupling proteins and AMPK–FoxO3A–MnSOD pathway in 3T3-L1 adipocytes Journal of Functional Foods Aug 2015 [SOD2]

NFkB is activated by multiple mechanisms in hairy cell leukemia Genes Chromosomes Cancer Jul 2015 [PITX1]

Systematic investigation of CMTM family genes suggests relevance to glioblastoma pathogenesis and CMTM1 and CMTM3 as priority targets Genes Chromosomes Cancer Jul 2015 [CMTM2]

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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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