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About This Item
NACRES:
NA.55
UNSPSC Code:
41106502
grade
Molecular Biology
form
liquid (aqueous solution)
packaging
pkg of 0.4 mL (06365779001), pkg of 1.0 mL (06365787001), pkg of 5 × 1.0 mL (06365809001)
manufacturer/tradename
Roche
technique(s)
transfection: suitable
storage temp.
2-8°C
usage
mL (suitable for 165 transfections)
General description
X-tremeGENE 9 DNA Transfection Reagent is a proprietary blend of lipids and other components supplied in 80% ethanol, filtered through 0.2 μm pore size membrane, and packaged in glass vials.
Application
X-tremeGENE™ 9 DNA Transfection Reagent is a non-liposomal multi-component reagent for experiments involving cellular analysis. Due to its extremely low cytotoxicity, minimal need for optimization, and the ability to provide high transfection efficiency in a wide range of commonly used cell lines even in the presence of serum, it is well suited for applications in all fields of cellular analysis.
X-tremeGENE™ 9 DNA Transfection Reagent is well suited for cellular analysis applications such as:
X-tremeGENE™ 9 DNA Transfection Reagent is well suited for cellular analysis applications such as:
- Expression of recombinant proteins for functional analysis.
- Physiological studies of metabolic pathways.
- Analysis of regulatory sequences using reporter gene assays.
- Gene expression assays.
- Cancer research studies.
- Target evaluation.
Features and Benefits
- Generate physiologically relevant results using a reagent with extremely low cytotoxicity for maximum post-transfection cell viability.
- Save time and eliminate multiple handling steps; simply dilute X-tremeGENE 9 DNA Transfection Reagent, incubate with plasmid DNA, and pipet the mixture directly onto your cells (with or without serum).
- Avoid time-consuming optimization procedures in commonly used cell lines.
Physical form
Supplied in 80% ethanol and sterile-filtered through 0.2 μm pore size membrane.Number of Tests: Using the standard procedure, 1 ml of X-tremeGENE 9 DNA Transfection Reagent can be used to perform up to 6,600 transfections in 96-well plates using 3:1 ratio and up to 10,000 transfections using 2:1 ratio.
Analysis Note
Each lot of X-tremeGENE™ 9 DNA Transfection Reagent is carefully tested following established quality procedures to ensure that the product is consistently performing according to specifications. During quality testing, cells are transfected with a reporter gene vector DNA using X-tremeGENE™ 9 DNA Transfection Reagent (ratio 3:1 μl/μg DNA). Reporter gene activity is monitored via chemiluminescent detection. Using a standard curve, the total amount of recombinant protein is determined per well in order to meet specification.
Other Notes
For life science research only. Not for use in diagnostic procedures.
Legal Information
X-tremeGENE is a trademark of Roche
signalword
Danger
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 2
Storage Class
3 - Flammable liquids
wgk
WGK 1
flash_point_f
334.4 °F
flash_point_c
168 °C
hcodes
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Leonardo Freire-de-Lima et al.
Proceedings of the National Academy of Sciences of the United States of America, 108(43), 17690-17695 (2011-10-19)
The process termed "epithelial-mesenchymal transition" (EMT) was originally discovered in ontogenic development, and has been shown to be one of the key steps in tumor cell progression and metastasis. Recently, we showed that the expression of some glycosphingolipids (GSLs) is
L C Costantini et al.
Neuroscience, 89(2), 505-513 (1999-03-17)
To investigate the role of neurotrophins in the initial formation of striatal patch versus matrix, the spatial and temporal expression of trkB receptors was examined using immunohistochemistry. Polyclonal antibodies, against the C-terminus or the tyrosine kinase domain, revealed trkB-immunoreactive cells
Piroon Jenjaroenpun et al.
BMC genomics, 10 Suppl 3, S9-S9 (2010-01-09)
DNA triplexes can naturally occur, co-localize and interact with many other regulatory DNA elements (e.g. G-quadruplex (G4) DNA motifs), specific DNA-binding proteins (e.g. transcription factors (TFs)), and micro-RNA (miRNA) precursors. Specific genome localizations of triplex target DNA sites (TTSs) may
Lauren Rouleau et al.
Free radical biology & medicine, 95, 308-322 (2016-04-03)
We investigated the mechanism of selective ascorbate-induced cytotoxicity in tumor cells, including Hep G2 cells, compared to primary hepatocytes. H2O2 formation was required for ascorbate cytotoxicity, as extracellular catalase treatment protected tumor cells. H2O2 generated by glucose oxidase treatment also
Daniel F Comiskey et al.
Nucleic acids research, 43(8), 4202-4218 (2015-04-08)
Genotoxic stress induces alternative splicing of the oncogene MDM2 generating MDM2-ALT1, an isoform attributed with tumorigenic properties. However, the mechanisms underlying this event remain unclear. Here we explore MDM2 splicing regulation by utilizing a novel minigene that mimics endogenous MDM2
Articles
转染是将DNA、RNA或蛋白质引入真核细胞的过程，用于研究和调节基因表达。因此，转染技术和实验方案作为分析工具，有助于表征遗传功能、蛋白质合成、细胞生长和发育。
Genetic engineering enables large-scale expression and isolation of recombinant proteins for research purposes.
Protocols
利用X-tremeGENE™ 转染试剂转染常见细胞系的实验方案
质粒的瞬时共转染是一种细胞蛋白互作研究、转录因子研究和shRNA编码质粒基因敲减研究的常用方法。
约转染前24小时接种细胞，确保细胞处于最佳密度（7090 %融合度）。
约转染前24小时接种转染细胞，确保细胞处于最佳密度（7090 %融合度）。
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
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