E-PAGE™ Midi Protein Gels, 3.7 mm
E-PAGE™ Midi Protein Gels (EP04808 and EP09606) orders may have a longer lead time than normal.
E-PAGE™ Midi Protein Gels, 3.7 mm
Invitrogen™

E-PAGE™ Midi Protein Gels, 3.7 mm

E-PAGE™ Gels are self-contained, pre-cast gels that include a gel matrix and electrodes packaged inside a disposable cassette.
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Catalog NumberWellsGel Percentage
EP0480848-well8%
EP0960696-well6%
Catalog number EP04808
Price (KRW)
624,000
Online offer
Ends: 31-Dec-2025
734,000
Save 110,000 (15%)
Each
Add to cart
Wells:
48-well
Gel Percentage:
8%
Price (KRW)
624,000
Online offer
Ends: 31-Dec-2025
734,000
Save 110,000 (15%)
Each
Add to cart
E-PAGE Gels are self-contained, pre-cast gels that include a gel matrix and electrodes packaged inside a disposable cassette. Protein separation on an E-PAGE Gel requires an EBase Integrated Device, a compact and automated platform designed for medium- and high-throughput electrophoresis.

Each E-PAGE 8% 48-well gel contains 48 sample lanes and 4 marker lanes with a 3.2-cm separation length. E-PAGE 48-well gels can be loaded with a 12- or 8-channel pipettor or 4- or 8-tip robotic system (Figure 1).

Each E-PAGE 6% 96-well gel contains 96 sample lanes and 8 marker lanes with a 1.6-cm separation length. The well openings of the cassette are compatible with the standard 96-well plate format and can be conveniently loaded with a multichannel pipettor or 8-, 12-, or 96-tip liquid-handling robotic device (Figure 2).

Both E-PAGE 48 and 96 cassettes can be opened to remove the gel for downstream staining or blotting (Figures 3 and 4). In addition, each cassette is labeled with an individual barcode to facilitate identification of the gel using commercial barcode readers.

More about the E-PAGE precast gel system
The Invitrogen E-PAGE precast gel system is designed for fast, mess-free medium- and high-throughput protein electrophoresis. It consists of the E-PAGE precast gels, E-Base Integrated devices for running the gels, and free E-Editor 2.0 software for image analysis.

The all-in-one E-Gel Power Snap Plus Electrophoresis System is designed for fast and convenient high-throughput gel electrophoresis. With dry precast E-PAGE gel technology, you can run protein samples in as little as 14 minutes. The device arrives with pre-programmed protocols for both E-PAGE gel types.

For Research Use Only. Not for use in diagnostic procedures.
Specifications
Gel Thickness3.7 mm
Length (Metric)8 cm
Mode of SeparationMolecular Weight
Product LineE-PAGE
Quantity8 gels (1 kit)
Sample Loading VolumeUp to 15 μL
Shelf Life9 Months
Shipping ConditionRoom Temperature
Storage RequirementsStore at room temperature, do not allow the temperature to drop below 4°C or rise above 40°C
Width (Metric)13 cm
For Use With (Equipment)E-BASE
Gel Percentage8%
Gel SizeMidi
Gel TypeE-PAGE
Separation Range20 to 220 kDa
Separation TypeDenaturing
Wells48-well
Unit SizeEach

Frequently asked questions (FAQs)

Are there robotic scripts for running E-Gel 48/96 or E-PAGE 48/96 gels?

Robotic scripts for running E-Gel 96 Agarose Gels and E-PAGE 96 Gels on Beckman Coulter's Biomek FX workstation can be found on our website at: www.thermofisher.com/egels (click the Labware Definitions link in the left navigation pane).

Find additional tips, troubleshooting help, and resources within our Nucleic Acid Purification and Analysis Support Center.

What is the difference between the EG and EP program for the E-Base system?

The EG program is to run E-Gel 96 and 48 gels, while the EP is to run the E-PAGE 96 and 48 gels.

Find additional tips, troubleshooting help, and resources within our Nucleic Acid Purification and Analysis Support Center.

What transfer buffer do I use to blot E-PAGE gels in a semi-wet transfer protocol (with the XCell II blot module)?

NuPAGE Transfer Buffer with 10% methanol provides optimal transfer of E-PAGE gels in the XCell II Blot Module. The NuPAGE Antioxidant is used in the transfer buffer for blotting reduced proteins and prevents the proteins from re-oxidizing. The Tris-Glycine Transfer Buffer has not been tested and it is not known as to what the transfer efficiencies would be like.

Find additional tips, troubleshooting help, and resources within our Protein Electrophoresis and Western Blotting Support Center.

What are some troubleshooting hints if there is high background after Coomassie staining of E-PAGE?

If you observe high background after Coomassie staining/destaining, here are some things to check:

It is very important to use 0.015% Coomassie R-250. Even using 0.03% will make Coomassie destaining more difficult.

The gel shouldn't be left in stain for more than 1 hour.

Increasing the destain time may reduce background.

Warming the gel and destain solution is also very important for best results.

Find additional tips, troubleshooting help, and resources within our Protein Electrophoresis and Western Blotting Support Center.

What is the function of the E-Editor 2.0 software?

The E-Editor 2.0 software allows you to quickly reconfigure digital images of E-Gel 48, E-Gel 96, E-PAGE 48 and E-PAGE 96 gel results for analysis and documentation. You can capture an image of the gel and then use the E-Editor 2.0 software to:
-Align and arrange the lanes in the image to any 48, 96, or 384 image
-Save the reconfigured image for further analysis
-Copy and paste selected lanes or the entire image into other applications for printing, saving, e-mailing, and/or publishing on the Web.

The E-Editor 2.0 does not take perform densitometry analysis from your gel images. The E-Editor 2.0 can be downloaded for free.

Find additional tips, troubleshooting help, and resources within our Protein Electrophoresis and Western Blotting Support Center.

View all E-PAGE™ Midi Protein Gels, 3.7 mm FAQs