CNBP RNAi (H00007555-R01)
CNBP RNAi
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CNBP RNAi Summary: | | | Specificity: | zinc finger protein 9 (a cellular retroviral nucleic acid binding protein) (ZNF9), mRNA |
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| Publications: | Antibody has at least 4 Background References. |
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| | Note: Not all species have been tested for usefulness with this product. Only those species listed have been tested. We cannot make any guarantees about additional reactivities which may or may not occur. |
View Additional CNBP Products | Unit Size: | 20 nmol (also available: 10 nmol) |
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| Concentration: | Concentration is not relevant for this product. Please see the protocols for proper use of this product. |
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Notes: This product is produced by and distributed for Abnova, a company based in Taiwan. Packaging: | Storage: | Aliquot and store at -20 °C or -80 °C. Avoid freeze-thaw cycles. |
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| Limitations: | This product is for research use only and is not approved for use in humans or in clinical diagnosis. Products are guaranteed for 6 months from date of receipt, except for peptides and proteins which are guaranteed for 3 months. |
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Background: Chimera RNA interference (chimera RNAi) is process by which small interfering RNA/DNA chimera triggers the destruction of mRNA for the original gene. The discovery work, design, and application of chimera RNAi has been pioneered by Professor Kaoru Saigo and Dr. Kumiko Ui-Tei at the University of Tokyo. Chimera RNAi has many advantages over the conventional siRNAs. First, it has been demonstrated to have reliable knock-down for over 10,000 human genes. Because the human genome is composed of an intricate, genetic network, chimera RNAi's unique design has successfully obviated the off-target effects including microRNA-based influence. Another advantage of the chimera RNAi technology is its effectiveness at low concentrations (0.5nM to 5nM); only mRNA is destroyed so genomic genes are not affected. Finally, having both the sense and anti-sense strands consisting RNA/DNA chimera, it offers much greater compound stability for streamlining in vitro and in vivo assays and applications while minimizing interferon induction and other adverse reactions.
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Images (1) Reviews (0) Related Products (7) Working with CNBP
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Jump to: Publications, Images, Protocols/Procedures, Ask a Question
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Working with CNBP
CNBP RNAi Images (1)
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Publications (4)CNBP RNAi Background References:- siDirect: highly effective, target-specific siRNA design software for mammalian RNA interference. Naito Y, Saigo K et al. Nucleic Acids Res. 2004 Jul 1;32 (Web Server issue):W124-9.
- Guidelines for the selection of highly effective siRNA sequences for mammalian chick RNA interference. Ui-Tei K, Saigo K et al. Nucleic Acids Res. 2004 Feb 9;32(3):936-48. Print 2004.
more... - dsCheck: highly sensitive off-target search software for double-stred RNA-mediated RNA interference. Naito Y, Morishita S et al. Nucleic Acids Res. 2005 Jul 1;33(Web Server issue):W589-91.
- Functional dissection of siRNA sequence by systematic DNA substitution: modified siRNA with a DNA seed arm is a powerful tool for mammalian gene silencing with significantly reduced off-target effect. Ui-Tei K, Naito Y, Zenno S et al. Nucleic Acids Res. 2008, Feb 11 [Epub ahead of print].
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