Roche X-tremeGENE 9 DNA Transfection Reagent Reference guide

Type
Reference guide
For life science research only. Not for use in diagnostic procedures.
X-TREMEGENE is a trademark of Roche.
Transfection procedureCell preparation for transfection
Plate cells approx. 24 hours before transfection
making sure cells are at optimal concentration
(70 – 90 % confluency).
Steps prior to transfection
Allow X-tremeGENE 9 DNA Transfection Reagent,
DNA and diluent (Opti:MEM I Reduced
Serum Medium or serum-free medium) to warm
to +15°C to +25°C, and vortex gently.
A detailed protocol is available in the online instructions for use at www.instructions.roche.com
For cell-type specific protocols, visit www.x-tremegene.roche.com. View the many successfully
used cell-type-specific transfection conditions in our customer feedback database.
Roche Diagnostics GmbH
Sandhofer Straße 116
68305 Mannheim
Germany
© 2011 Roche Diagnostics.
All rights reserved.
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X-tremeGENE 9 DNA Transfection Reagent
Quick Protocol
For products with Catalog Numbers:
06 366 511 001 | 06 365 779 001 | 06 365 787 001 | 06 365 809 001
Volumes of X-tremeGENE 9 DNA Transfection Reagent and amounts of DNA for various ratios
Ratio
Transfection Reagent : DNA
Minimal transfection
complex volume
Volume for a whole
96-well plate
Serum-free medium to a final volume of
100 µl 500 µl
3 : 1
X-tremeGENE 9 Transfection Reagent
3 µl 15 µl
DNA
1 µg 5 µg
6 : 1
X-tremeGENE 9 Transfection Reagent
6 µl 30 µl
DNA
1 µg 5 µg
6 : 2
X-tremeGENE 9 Transfection Reagent
6 µl 30 µl
DNA
2 µg 10 µg
Add transfection complex to the cells in a
dropwise manner.
Gently shake or swirl the wells or fl asks to
ensure even distribution over the entire plate.
Incubate cells for 18 72 hours before
measuring protein expression.
Place diluent in a sterile tube.
Add X-tremeGENE 9 DNA Transfection
Reagent to the diluent.
Add plasmid DNA. Pipet gently to mix.
Incubate for 15 min at +15°C to +25°C.
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Roche X-tremeGENE 9 DNA Transfection Reagent Reference guide

Type
Reference guide

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