Product: Cefprozil (monohydrate)
TCIRG1 RNAi Summary
| Specificity |
T-cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein a isoform 3 (TCIRG1), transcript variant 1, mRNA
|
| Gene |
TCIRG1
|
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 TCIRG1 RNAi
- a3
- Atp6i
- ATP6N1C
- ATP6N1Cspecific 116-kDa vacuolar proton pump subunit
- ATP6V0A3T-cell immune response cDNA 7
- OC-116 kDa
- OC116
- OC-116
- OC-116kDa
- OC116Vph1
- OPTB1
- Osteoclastic proton pump 116 kDa subunit
- Stv1
- T-cell immune regulator 1
- T-cell immune response cDNA7 protein
- T-cell, immune regulator 1
- T-cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein a
- T-cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3
- T-cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein aisoform 3
- T-cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 subunit A3
- TCIRG1
- TIRC7
- TIRC7ATPase, H+ transporting, 116kD
- Vacuolar proton translocating ATPase 116 kDa subunit a isoform 3
- vacuolar proton translocating ATPase 116 kDa subunit A
- V-ATPase 116 kDa isoform a3
- V-ATPase 116-kDa
- Vph1
- V-type proton ATPase 116 kDa subunit a isoform 3
- V-type proton ATPase 116 kDa subunit a
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.
