E-Gel™ SizeSelect™ II Agarose Gels, 2%
Discover our new Invitrogen E-Gel Agarose Gels with SYBR Safe DNA Stain—a safe alternative to ethidium bromide. Learn more »
E-Gel™ SizeSelect™ II Agarose Gels, 2%
Invitrogen™

E-Gel™ SizeSelect™ II Agarose Gels, 2%

Electrophoresis using E-Gel SizeSelect II Agarose Gels is a convenient method for accurate size selection of DNA libraries for next-generationRead more
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Catalog number G661012
Price (USD)
258.00
Each
Add to cart
Price (USD)
258.00
Each
Add to cart
Electrophoresis using E-Gel SizeSelect II Agarose Gels is a convenient method for accurate size selection of DNA libraries for next-generation sequencing (NGS) applications. With E-Gel SizeSelect II gels, you can separate and recover DNA for library construction in three easy steps: load, run, and retrieve.

E-Gel SizeSelect II agarose gels enable you to:
Save time—no need to prepare a gel and gel-purify after electrophoresis
Simplify DNA recovery—retrieve purified DNA directly from the recovery well with a pipette
Improve result consistency—achieve accurate and consistent size selection

Fast and accurate DNA size selection in three easy steps
DNA fragment library size selection with E-Gel SizeSelect II precast gels is a simple 3-step procedure that eliminates conventional gel purification. To extract the DNA band of interest, load the sample into the loading wells, run the gel until the band reaches the recovery wells, and retrieve the sample. The resulting fragment library demonstrates a sharp fragment cut-off and is ready for use in an NGS workflow without any need for re-purification. Multiple bands from the one loading well can be collected during the same gel run.

DNA fragment libraries extracted from E-Gel SizeSelect II gels are compatible with the Ion Torrent sequencing workflow.

Real-time control of the sample
SYBR Gold II DNA Gel Stain is incorporated into the gel itself, allowing you to visually monitor DNA band migration progress on the blue-light transilluminator of the E-Gel Power Snap Electrophoresis Device. The gel has reference marks for better control of the sample prior to the sample recovery step. If the target DNA passes the recovery well, the Reverse gel protocol allows for re-capture of the DNA band.

Nucleic acid markers
Learn more about our E-Gel DNA ladders ›

Enables better results
Even a short exposure of your DNA sample to UV light during visualization may lead to DNA damage. Using E-Gel SizeSelect II gels together with the blue-light transilluminator minimizes the risk of UV damage compared to a conventional gel purification workflow. The direct access to your sample from the retrieval well allows you to avoid excising gel band slices and the risk of losing your DNA during a gel purification step.

For Research Use Only. Not for use in diagnostic procedures.
Specifications
Compatible LaddersE-Gel™ Sizing DNA Ladder
Gel Percentage2%
Gel TypeE-Gel
Product TypeAgarose Gel
Stain TypeSYBR™ Gold
Wells7-well
Quantity10 gels
Shipping ConditionRoom Temperature
Unit SizeEach
Contents & Storage
Store at room temperature.

Frequently asked questions (FAQs)

My E-Gel agarose gel has speckles when viewed in the imager. What should I do?

Here are some suggestions:

- Try cleaning the cassettes with alcohol and Kimwipes wipers.
- Try cleaning the camera lens.
- Try to adjust the exposure time and brightness options of the documentation system you are using.

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

My sample is leaking from the wells when running my E-Gel agarose gels. What happened?

Please ensure that you have not overloaded the well and that the wells were not damaged during comb removal.

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

I accidentally stored my E-Gel agarose gels at 4 degrees C instead of room temperature. Can I still use them?

While we recommend storage at room temperature, these gels will still be usable. Bring the gels to room temperature prior to the run for optimal conditions.

Find additional tips, troubleshooting help, and resources within ourNucleic Acid Gel Electrophoresis and Blotting Support Center.

What loading buffer should I use for my E-Gel agarose gels?

Loading buffer is optional. Samples can be loaded directly into the wells if no buffer is used, or you can dilute them with deionized water or TE buffer. If you want to use a loading buffer, please see the recipes below:

E-Gel agarose gels (including EX)
10 mM Tris-HCl, pH 7.5
1 mM EDTA
0.005% bromophenol blue
0.005% xylene cyanol FF
E-Gel CloneWell II and E-Gel SizeSelect II agarose gels
10 mM Tris-HCl, pH 7.5
1 mM EDTA

Alternatively, you can use 10X BlueJuice Gel Loading Buffer or TrackIt Loading Buffer. Dilute this buffer 50- to 200-fold to obtain optimal results with E-Gel agarose gels.

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

How do I acquire and analyze data for my E-Gel agarose gels?

We offer our E-Editor Software, which can help you align images after a gel run. The E-Editor 2.0 Software is only available for PCs, but the older E-Gel 96 Editor software is still available for the Mac operating system and can align images from E-Gel 96 and E-PAGE 96 agarose gels. However, the original software is not compatible with E-Gel 48 or E-PAGE 48 agarose gels. Please go to www.thermofisher.com and enter "E-Editor software" in the main search to download the E-Editor Software. You can use the E-Gel Imager System for data analysis.

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