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ABOUT US > Technology >>SYDOTS

  1. What is SYDOTS?

    A new technique under development in Viagene Biotech provides novel procedures and apparatus for determining the stability of DNA, RNA and oligonucleotides.

  2. What can this technique be used for?

    Determining the stability of nucleic acids is a useful technique in the analysis of gene expression at the transcriptional level. S1 mapping and ribonuclease protection assays (RPA), based on the principle of the resistance of DNA/RNA or RNA/RNA duplexes to Nuclease S1 or ribonucleases (RNase), are used to quantify specific RNAs via duplex formation of RNAs and radioisotope-labeled probes, and the degradation of unhybridized probes and RNAs with nucleases or RNase at the end of the reaction. The surviving DNA-RNA or RNA-RNA duplexes are then separated by gel-electrophoresis and visualized by autoradiography. These detection techniques can also be used to map the positions of introns and to identify the locations of 5' and 3' ends of mRNAs on cloned DNA templates.

    Determining the stability of small nucleic acids or modified nucleic acids is important in the field of drug discovery, because the therapeutic application of small DNA/RNA molecules will be largely dependent on improvements in their biostability and efficacy. It has been reported that stabilized synthetic oligodeoxynucleotides (ODNs) and oligooxynucleotides have the potential to be used as therapeutic agents. Several antisense ODNs have been FDA-approved or are currently undergoing preclinical and clinical investigation. Decoy ODNs, which are double-stranded ODNs (dsODNs) containing the critical transcription factor-recognizing sequences found in cis-elements of selected genes, have the capacity to induce artificial modulation of gene expression at the transcriptional level. RNA decoys also have been shown to be capable of binding to transcription factors via aptameric interactions. Furthermore, gene-specific short interfering (si)RNAs have been shown to inhibit gene transcription. When pursuing structural and chemical modifications of ODNs or siRNA, the ideal modification should make these small molecules resistant to degradation by nucleases and RNases, and preserve the specific molecular interactions of these molecules with the target DNA/RNA or transcription factors.

     

    * This design and technology are patent pending.

 

 


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