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Roche

X-tremeGENE siRNA Transfection Reagent

Polymer reagent for delivering siRNA to common cell lines

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About This Item

Codice UNSPSC:
41106502
NACRES:
NA.55

Grado

for molecular biology

Livello qualitativo

impiego

sufficient for 2,000 transfections (04476115001)
sufficient for 400 transfections (04476093001)

Confezionamento

pkg of 1 mL (04476093001 [1 mg/ml])
pkg of 5 × 1 mL (04476115001 [5 x 1 mg/ml])

Produttore/marchio commerciale

Roche

Concentrazione

1 mg/mL

tecniche

transfection: suitable

Condizioni di spedizione

wet ice

Temperatura di conservazione

2-8°C

Descrizione generale

Short interfering RNA (siRNA) can be directly introduced into cells by transfection. A lipid-based transfection reagent, such as X-tremeGENE siRNA Transfection reagent, can provide a convenient, reliable, and efficient vehicle for delivering siRNAs into animal cells, enabling the study of cellular and functional consequences of gene knockdown.
This innovative reagent forms a complex with siRNA, as well as with mixtures of siRNA and plasmid DNA (cotransfection), and efficiently delivers the nucleic acids into animal cells to induce gene silencing. Transfection is achieved in just a few steps: mix and incubate diluted transfection reagent with diluted siRNA, then add this complex to cells. Because X-tremeGENE siRNA Transfection Reagent functions exceptionally well in the presence or absence of serum and demonstrates low cytotoxicity, it can be used without media changes. The product is animal-component free.

Contents

Solution filtered through 0.2 μm pore size membrane, supplied in polypropylene tubes.

Applicazioni

X-tremeGENE siRNA Transfection Reagent efficiently delivers short interfering RNA (siRNA) into many commonly used cell types including HeLa, NIH 3T3, HEK-293, CHO-K1, and COS-7, and several hard-to-transfect cell lines, such as HT29, a human adenocarcinoma cell line.

Caratteristiche e vantaggi

  • Knock down gene expression over 90% in many different cell types.
  • Maximize experimental flexibility with a single reagent for siRNA- and cotransfection-based gene-knockdown experiments.
  • Produce meaningful results using a reagent that exhibits low cytotoxicity, ensuring that the cellular effects you observe are due to the transfected siRNA rather than the transfection procedure.
  • Work with or without serum, avoiding medium changes (e.g., to serum-free medium) before or after transfection.;

X-tremeGENE siRNA Transfection Reagent is a proprietary blend of lipids and other components, free of animal products.

Qualità

Activity assay: X-tremeGENE siRNA Transfection Reagent (1 - 2.5 μl) is combined with siRNA (0.1 - 0.35 μg) that is specific for the HPRT housekeeping gene. The mixture is used to transfect HEK-293 cells (in a monolayer, 30 - 50% confluent) in the presence of 10% fetal bovine serum (FBS). Following transfection, the decrease of HPRT mRNA cells is determined with the LightCycler® Real-Time PCR System. A knockdown efficiency of 70 - 95% is typically observed when mRNA is measured.

Cytotoxicity analysis: HEK-293 cells are exposed to siRNA/X-tremeGENE siRNA Reagent complexes for 72 hours in the presence of serum, without a media change. Cytotoxicity is then tested by analyzing the cells with the WST-1 Cell Proliferation Reagent (Roche).

Altre note

For life science research only. Not for use in diagnostic procedures.

Note legali

X-tremeGENE is a trademark of Roche

Codice della classe di stoccaggio

12 - Non Combustible Liquids

Classe di pericolosità dell'acqua (WGK)

nwg

Punto d’infiammabilità (°F)

does not flash

Punto d’infiammabilità (°C)

does not flash


Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

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Mei Zhan et al.
Experimental hematology, 35(7), 1015-1025 (2007-06-26)
MicroRNAs (miRNAs) are an abundant class of small noncoding RNAs that regulate diverse cellular functions by sequence-specific inhibition of gene expression. We determined miRNA expression profile during erythroid differentiation and putative roles in erythroid differentiation. The expression profile of 295
Christina Lohmann et al.
Analytical biochemistry, 366(2), 117-125 (2007-06-09)
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Virology, 365(2), 285-291 (2007-05-15)
Little is known about specific naturally occurring mutations of hepatitis B virus (HBV) and underlying mechanisms of their association with fulminant hepatitis. A HBV clone isolated from a patient with fulminant hepatitis was analyzed, and the features of the particular
Tong Tang et al.
Journal of the American College of Cardiology, 55(14), 1476-1486 (2010-04-03)
This study sought to test the hypothesis that pressure stress of the adenylyl cyclase 6-deleted (AC6-KO) heart would result in excessive hypertrophy, early dilation and dysfunction, and increased fibrosis. Cardiac-directed AC6 expression attenuates left ventricular (LV) hypertrophy and dysfunction in
J S Ungerstedt et al.
Proceedings of the National Academy of Sciences of the United States of America, 102(3), 673-678 (2005-01-08)
This study examines the basis of resistance and sensitivity of normal and transformed cells to histone deacetylase inhibitor (HDACi)-induced cell death, specifically the role of caspases and thioredoxin (Trx). An important attribute of HDACis is that they induce cancer cell

Articoli

Small inhibitory RNAs offer easy gene expression knockdown in mammalian cells, revolutionizing gene research.

Transfection introduces genetic material into cells, aiding research in gene expression and cell biology.

This brief webinar provides an overview of what transfection is and the methods that are used to introduce DNA or RNA into eukaryotic cells.

Genetic engineering enables large-scale expression and isolation of recombinant proteins for research purposes.

Protocolli

X-tremeGENE™ siRNA Transfection Reagent Protocol & Troubleshooting

Protocols for Transfecting Common Cell Lines with X-tremeGENE™ Transfection Reagents

Contenuto correlato

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