Product: Propafenone (D9 hydrochloride)
DNA Polymerase epsilon subunit 3 RNAi Summary
| Specificity |
polymerase (DNA directed), epsilon 3 (p17 subunit) (POLE3), mRNA
|
| Gene |
POLE3
|
Applications/Dilutions
| Application Notes |
This RNAi causes protein knockdown.
|
Packaging, Storage & Formulations
| Storage |
Store at -20C. Avoid freeze-thaw cycles.
|
Notes
This product is produced by and distributed for Abnova, a company based in Taiwan.
Alternate Names for DNA Polymerase epsilon subunit 3 RNAi
- Arsenic-transactivated protein
- asTP
- CHARAC17arsenic transactivated protein
- CHRAC-17
- CHRAC17Ybl1
- Chromatin accessibility complex 17 kDa protein
- DNA polymerase epsilon p17 subunit
- DNA polymerase epsilon subunit 3
- DNA polymerase epsilon subunit p17
- DNA polymerase II subunit 3
- EC 2.7.7.7
- histone fold protein CHRAC17
- huCHRAC17
- p17
- polymerase (DNA directed), epsilon 3 (p17 subunit)
- YBL1
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 RNAis 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.
