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RNAi Duplex Oligos
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United States
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idt
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Updated:
9/5/2024
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    References

     
    1.Unlocking the potential of the human genome with RNA interference. Hannon, G.J. and Rossi, J.J. Nature, 431, 371-378 (2004)
     
    2.Mechanisms of gene silencing by double-stranded RNA. Meister, G. and Tuschl, T. Nature, 431, 343-349 (2004).
     
    3.TRBP recruits the Dicer complex to Ago2 for microRNA processing and gene silencing. Chendrimada, T.P., Gregory, R.I., Kumaraswamy, E., Norman, J., Cooch, N., Nishikura, K. and Shiekhattar, R. Nature, 436, 740-744 (2005).
     
    4.Synthetic dsRNA Dicer substrates enhance RNAi potency and efficacy. Kim, D.H., Behlke, M.A., Rose, S.D., Chang, M.S., Choi, S. and Rossi, J.J. Nat Biotechnol, 23, 222-226 (2005).
     
    5.Functional polarity is introduced by Dicer processing of short substrate RNAs. Rose, S.D., Kim, D.H., Amarzguioui, M., Heidel, J.D., Collingwood, M.A., Davis, M.E., Rossi, J.J. and Behlke, M.A. Nucleic Acids Res, 33, 4140-4156 (2005).
     
    6.siRNA function in RNAi: a chemical modification analysis. Chiu, Y.L. and Rana, T.M. RNA, 9, 1034-1048 (2003).
     
    7.Sequence, chemical, and structural variation of small interfering RNAs and short hairpin RNAs and the effect on mammalian gene silencing. Harborth, J., Elbashir, S.M., Vandenburgh, K., Manninga, H., Scaringe, S.A., Weber, K. and Tuschl, T. Antisense Nucleic Acid Drug Dev, 13, 83-105 (2003).
     
    8.Activation of the mammalian immune system by siRNAs. Marques, J.T. and Williams, B.R. Nat Biotechnol, 23, 1399-1405 (2005).
     
    9.A structural basis for discriminating between self and nonself double-stranded RNAs in mammalian cells. Marques, J.T., Devosse, T., Wang, D., Zamanian-Daryoush, M., Serbinowski, P., Hartmann, R., Fujita, T., Behlke, M.A. and Williams, B.R. Nat Biotechnol, 24, 559-565 (2006).
     
    10.Design of noninflammatory synthetic siRNA mediating potent gene silencing in vivo. Judge, A.D., Bola, G., Lee, A.C. and MacLachlan, I. Mol Ther, 13, 494-505 (2006).
     
    11.Progress towards in vivo use of siRNAs. Behlke, M.A. Mol Ther, 13, 644-670 (2006).
     
    12.Rational design and in vitro and in vivo delivery of Dicer substrate siRNA. Amarzguioui, M., Lundberg, P., Cantin, E., Hagstrom, J.E., Behlke, M.A. and Rossi, J.J. Nature Protocols, 1, 508-517 (2006).
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    About IDT

    Integrated DNA Technologies (IDT) is a leader in manufacturing and developing products for the research and diagnostics life science market. IDT serves the areas of academic research, biotechnology, and pharmaceutical development. IDT was founded by Dr Joseph Walder in 1987. Since then, its development has been guided by an uncompromising approach to quality, a belief in the value of good service, and a determination to minimize consumer costs.

    Serving over 80,000 life sciences researchers, IDT is widely recognized as the industry leader in custom oligonucleotides due to its capabilities in:

    Analytical Sophistication—IDT pioneered the use of high throughput quality control (QC) methods and is the only oligonucleotide manufacturer to offer purity guarantees and 100% QC. Every oligonucleotide is analyzed by mass spectrometry and purified oligonucleotides receive further analysis by CE and HPLC.
    Design Engineering—IDT maintains an engineering division dedicated to advancing synthesis, processing technology, and automation. An in-house machine shop provides rapid prototyping and custom part design/control.
    Customer Support—IDT received over 100,000 calls last year with an average wait time of only 8 seconds.
    Reagent and Input Control—IDT receives all solvents in large bulk containers, runs QC on all incoming materials, and performs bulk reagent formulation and functional QC on all reagents.
    IDT has over 700 employees serving our worldwide customer base from headquarters in Coralville, Iowa, and facilities in San Diego, California; Leuven, Belgium; and Singapore.
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