RNAi Resource: siRNA Transfection
RNA Interference (RNAi) is utilized in many eukaryotic cells including those found in mammals, which enables protein complex called RISC associate with double-stranded RNA molecules and activate sequence-specific gene silencing (target mRNA degradation).
The chain of reactions involved in cells in this manner enables DNA to be transcripted into RNA, which is then translated into proteins. RNAi research is a valuable process in gene expression studies not only for the studies using cell cultures and living organisms (in vivo siRNA), but in synthetic production of the siRNA that may eventually be introduced into cells to induce gene suppression as disease-gene-targeted RNAi Therapeutics.
RNAi has also been known as post-transcriptional gene silencing, and in 2006, two scientists by the name of Andrew Fire and Craig Mello earned the Nobel Prize in physiology and medicine for their work in RNAi studies.
Transfection of siRNA is used in biology laboratories to experimentally induce gene silencing (RNAi) in cultured cells in vitro and animals in vivo. Scientists perform gene expression studies, functional genomics, gene characterization, and discovery of signalling gene pathways by introduction of extracellular molecules, such as small interferring RNA (siRNA), microRNA (miRNA), plasmid DNA expressing shRNA, messenger RNA (mRNA).
Transient transfection term refer to introduction of siRNA (or miRNA) molecule inside the cell without affecting its genomic DNA (transient expression), while stable transfection happens at incorporation of plasmid DNA into genome of the host cell (stable expression).
There are various cell transfection methods, including chemical transfection, electroporation, sonoporation, magnetofection, and gene gun injection. Commonly used transfection kits and reagents are nanoparticle-, lipid-, liposome-, and polymer-based. Pre-optimizized transfection kits and products are manufactured by Altogen Biosystems.
Optimized siRNA transfection kits include:
In Vivo Transfection Reagents HEK-293 Transfection Reagent MEF Transfection Reagent HepG2 Transfection Reagent Cos7 Transfection Reagent A549 Transfection Reagent HUVEC Transfection Reagent LNCaP Transfection Reagent MCF-7 Transfection Reagent
Transfection Links:
WikiPedia: What is transfection?
Biology Research Services: Stably-Expressing Cell Line Generation
RNAi Services
In Vivo siRNA Transfection Kits and Reagents
Optimized cell-specific siRNA transfection reagents:
hamster ovary epithelial cells
human hepatocellular carcinoma cells
mammary epithelial cancer cells
human breast cancer cells
colorectal adenocarcinoma cells
human osteosarcoma cells
human hepatoma cells
umbilical vein endothelial cells
breast cancer cells
murine embryonic fibroblast cells
mouse embryonic stem cells
tracheal gland cells
human diploid fibroblast cells
mouse fibroblast cells
normal rat kidney epithelial cells
human neuroblastoma cells
bone marrow neuroblastoma cells
neuroblastoma cells
human adrenocortical carcinoma cells
glioblastoma cells
The chain of reactions involved in cells in this manner enables DNA to be transcripted into RNA, which is then translated into proteins. RNAi research is a valuable process in gene expression studies not only for the studies using cell cultures and living organisms (in vivo siRNA), but in synthetic production of the siRNA that may eventually be introduced into cells to induce gene suppression as disease-gene-targeted RNAi Therapeutics.
RNAi has also been known as post-transcriptional gene silencing, and in 2006, two scientists by the name of Andrew Fire and Craig Mello earned the Nobel Prize in physiology and medicine for their work in RNAi studies.
Transfection of siRNA is used in biology laboratories to experimentally induce gene silencing (RNAi) in cultured cells in vitro and animals in vivo. Scientists perform gene expression studies, functional genomics, gene characterization, and discovery of signalling gene pathways by introduction of extracellular molecules, such as small interferring RNA (siRNA), microRNA (miRNA), plasmid DNA expressing shRNA, messenger RNA (mRNA).
Transient transfection term refer to introduction of siRNA (or miRNA) molecule inside the cell without affecting its genomic DNA (transient expression), while stable transfection happens at incorporation of plasmid DNA into genome of the host cell (stable expression).
There are various cell transfection methods, including chemical transfection, electroporation, sonoporation, magnetofection, and gene gun injection. Commonly used transfection kits and reagents are nanoparticle-, lipid-, liposome-, and polymer-based. Pre-optimizized transfection kits and products are manufactured by Altogen Biosystems.
Optimized siRNA transfection kits include:
In Vivo Transfection Reagents HEK-293 Transfection Reagent MEF Transfection Reagent HepG2 Transfection Reagent Cos7 Transfection Reagent A549 Transfection Reagent HUVEC Transfection Reagent LNCaP Transfection Reagent MCF-7 Transfection Reagent
Transfection Links:
WikiPedia: What is transfection?
Biology Research Services: Stably-Expressing Cell Line Generation
RNAi Services
In Vivo siRNA Transfection Kits and Reagents
Optimized cell-specific siRNA transfection reagents:
hamster ovary epithelial cells
human hepatocellular carcinoma cells
mammary epithelial cancer cells
human breast cancer cells
colorectal adenocarcinoma cells
human osteosarcoma cells
human hepatoma cells
umbilical vein endothelial cells
breast cancer cells
murine embryonic fibroblast cells
mouse embryonic stem cells
tracheal gland cells
human diploid fibroblast cells
mouse fibroblast cells
normal rat kidney epithelial cells
human neuroblastoma cells
bone marrow neuroblastoma cells
neuroblastoma cells
human adrenocortical carcinoma cells
glioblastoma cells
Labels: biology, cancer, cell transfection, gene, in vivo, research services, RNAi, service, siRNA, stable transfection, stem cells, transfection, transfection efficiency

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