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View additional product information for E-Gel™ 96 Agarose Gels - FAQs (G720802, G720842, G720801, G700801, G700802, G720841)
29 product FAQs found
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.
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.
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.
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.
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.
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.
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.
E-Gel 48 and E-Gel 96 gels contain a proprietary neutral-pH internal buffer system with special high capacity and low conductivity features. There are no ion exchange matrices.
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p>High-throughput E-Gel agarose gels have staggered wells, and are based on a neutral-pH internal buffer system as opposed to an ion exchange matrix. High-throughput E-Gel agarose gels cannot be opened, and should be run on the E-Gel E-Base system.
Find additional tips, troubleshooting help, and resources within our Nucleic Acid Purification and Analysis Support Center.
If you do not have enough samples to use all the wells, fill each empty well with the same volume of water as the loaded samples. For E-Gel CloneWell II agarose gels and E-Gel SizeSelect II agarose gels, it is important to add the water according to the respective manual.
Find additional tips, troubleshooting help, and resources within our Nucleic Acid Gel Electrophoresis and Blotting Support Center.
Our E-Gel agarose gels can be used for either DNA or RNA separation. RNA separation occurs under non-denaturing or denaturing conditions. Please note, our gels are not QC tested for the presence of RNases. See our suggestions below for running your non-denaturing or denaturing samples:
Non-denaturing conditions
1. Mix RNA sample with 15 µL of RNase-free water.
2. Do not heat. Load the entire sample onto the E-Gel agarose gel.
3. Electrophorese for 30 min.
Denaturing conditions
1. Mix 15 µL of RNA loading buffer with 1-5 µL of RNA (1-5 µg).
2. Heat samples at 65 degrees C for 10 min to denature RNA.
3. Place samples on ice immediately after heating.
4. Load entire sample onto E-Gel agarose gel.
5. Electrophorese for 30 min.
Note:
- The only denaturing agent that is compatible with the E-Gel system is formamide, 50-95%. Heating the sample for 5 min at 65 degrees C should be sufficient for denaturing. Using other denaturing agents like glyoxal, formaldehyde, or urea will result in very poor separation and band morphology on E-Gel agarose gels.
- Additionally, we do not recommend running samples with RNA loading buffer on the same gel as samples loaded with water.
- E-Gel EX Double Comb agarose gels and E-Gel Double Comb agarose gels with SYBR Safe stain have not been tested for use in RNA applications.
Find additional tips, troubleshooting help, and resources within our Nucleic Acid Purification and Analysis Support Center.
We recommend using the E-Gel Opener (Cat. No. G530001) for the SYBR and ethidium bromide E-Gel agarose gels. The E-Gel EX agarose gels, E-Gel SizeSelect agarose gels, and E-Gel GO! agarose gels can be opened with the Gel Knife (Cat. No. EI9010). We do not recommend opening the E-Gel 48 agarose gels or the E-Gel 96 agarose gels.
Find additional tips, troubleshooting help, and resources within our Nucleic Acid Purification and Analysis Support Center.
To create a bufferless system, each E-Gel cassette contains two unique ion exchange matrices that lie between the running gel and the electrodes. The ion exchange matrices provide a buffer-ion reservoir that supplies a continuous flow of Tris, acetate, and dye ions throughout the gel. This patented technology results in a sustained electric field with enhanced buffering capacity. E-Gel gels thus eliminate the need for you to prepare and dispose of liquid buffer, thus saving time and waste.
Find additional tips, troubleshooting help, and resources within our Nucleic Acid Gel Electrophoresis and Blotting Support Center.
The E-Gel agarose gel system is a precast bufferless TAE system that uses ion exchange matrices. The gels themselves are enclosed within a semi-UV-transparent cassette. This patented technology results in a sustained electric field with enhanced buffering capacity. E-Gel gels thus eliminate the need for you to prepare and dispose of liquid buffer, thus saving time and waste.
Find additional tips, troubleshooting help, and resources within our Nucleic Acid Purification and Analysis Support Center.
Pre-run is no longer necessary for any of our E-Gel agarose gels.
Find additional tips, troubleshooting help, and resources within our Nucleic Acid Purification and Analysis Support Center.
E-Gel agarose gels are routinely used in-house in R&D and manufacturing for RNA analysis with excellent results. However, the gels are not guaranteed to be “RNAse-free”. The manufacturing process is designed to avoid contamination of any type, but not RNAses specifically.
If you do want to try it, any loading buffer that would be used for non-denaturing RNA electrophoresis should be fine for E-Gel agarose gels. Depending on your application, these gels may or may not be suitable for use.
Find additional tips, troubleshooting help, and resources within our Nucleic Acid Purification and Analysis Support Center.
Several advantages of the E-Gel 96 are listed below:
1. They are pre-cast - no gels to pour.
2. They are bufferless - no buffers to prepare or dispose; no mess to clean up.
3. They are pre-stained - no staining/destaining procedures, no handling of toxic staining agents.
4. Bases are SBS (Society for Biomolecular Screening) standard compatible for 96-well format - they fit most robotic platforms designed for standard microtiter plates.
5. Patented staggered-well format offers double the run length per sample compared to standard 96-well gels, while still remaining compatible with standard 8-, 12-, or 96-tip robotic loading systems.
Find additional tips, troubleshooting help, and resources within our Nucleic Acid Purification and Analysis Support Center.
The E-Editor 2.0 Software can be downloaded for free from the Thermo Fisher Scientific website (search for 'e-editor 2.0').
Find additional tips, troubleshooting help, and resources within our Nucleic Acid Purification and Analysis Support Center.
Do not run E-Gel agarose gels longer than 40 min for the single comb gels or longer than 20 min for the double comb gels as longer run times will cause ions to get depleted and will damage the gel. Do not run E-Gel 48 agarose gels longer than 30 min or E-Gel 96 agarose gels longer than 20 min.
Find additional tips, troubleshooting help, and resources within our Nucleic Acid Purification and Analysis Support Center.
All E-Gel gels are labeled with expiration dates.
Find additional tips, troubleshooting help, and resources within our Nucleic Acid Purification and Analysis Support Center.
Potential problems include:
- Loading too much DNA. Do not load more than the recommended amount.
- Samples with a high salt concentration. Samples containing > 50 mM NaCl, 100 mM KCl, 10 mM acetate ions, or 10 mM EDTA will cause loss of resolution.
- Samples may have been diluted in TAE instead of TE or water.
- Samples may have been pre-run; pre-running is not recommended for any of our E-Gel agarose gels.
- Sample was not properly loaded or had a very low volume of sample loaded. Load the recommended sample volume based on the gel type and loading method. For proper band separation, we recommend keeping sample volumes uniform.
- Bubbles may have been introduced while loading the samples. Bubbles will cause band distortion. Load deionized water or TE into any empty wells, and avoid introducing bubbles.
- A longer electrophoresis run time was used. Do not run the gel longer than the recommended time for each gel type. Longer run times cause an increase in the current, resulting in poor band migration or a melted gel. We recommend that you run single comb gels for 25-30 min (double comb gels 15-20 min) for straighter patterns. Do not run single comb gels longer than 40 minutes (20 minutes for double comb), or the gel will be damaged and resolution will be poor.
- Voltage or current too high. This should not be an issue with the E-Gel PowerBase power supply, which is pre-set with the proper conditions. However, researchers using the old E-Gel Base (the one that plugged into a separate power supply) should ensure that they run the gel at 60 to 70 volts (constant voltage) or 40-50 mA (constant current). Do not allow the current to exceed 60 mA.
- For E-Gel 96 Agarose Gels being run on an E-Base device, be sure you are running on the “EG” program rather than the “EP” program designed for E-PAGE gels.
- The gel was not electrophoresed immediately after sample loading (for best results, run gel within 1 min of loading).
- The gel may have been used beyond its expiration date. Check the expiration date.
Find additional tips, troubleshooting help, and resources within ourNucleic Acid Gel Electrophoresis and Blotting Support Center.
The agarose used in the 0.8%, 1.2% and 2% E-Gel agarose gels is molecular biology grade, with a normal melting point and less than 0.25% ash content. For the 4% E-Gel agarose gels, we use a special high-resolution agarose.
Find additional tips, troubleshooting help, and resources within our Nucleic Acid Purification and Analysis Support Center.
The E-Gel agarose gel system uses TAE buffer.
Find additional tips, troubleshooting help, and resources within our Nucleic Acid Purification and Analysis Support Center.
We do not recommend using the E-Gel Power Snap Electrophoresis Device to image pour-your-own gels.
Find additional tips, troubleshooting help, and resources within our Nucleic Acid Purification and Analysis Support Center.
We do not recommend using the E-Gel Power Snap Electrophoresis Device to run pour-your-own gels.
Find additional tips, troubleshooting help, and resources within our Nucleic Acid Purification and Analysis Support Center.
Yes, both the E-Gel GelCapture Acquisition Software and E-Gel GelQuant Express Analysis Software applications are compatible with Windows 10; however, the E-Gel GelQuant Express Analysis Software will require the purchase of an E-Gel Imager Quantitation USB dongle (Cat. No. 4466610):
https://www.thermofisher.com/order/catalog/product/4466610
Please visit the following link (https://www.thermofisher.com/us/en/home/life-science/dna-rna-purification-analysis/nucleic-acid-gel-electrophoresis/e-gel-electrophoresis-system/e-gel-imager-system/e-gel-software.html) and follow the instructions to download the software.
Note: Please make sure that you download the correct version of the E-Gel GelCapture Software based on the serial number of your instrument.
Find additional tips, troubleshooting help, and resources within our Nucleic Acid Purification and Analysis Support Center.
Each program on the E-Gel Power Snap Electrophoresis Device is optimized to obtain the best possible results. The device does not offer user-adjustable voltage functionality.
Find additional tips, troubleshooting help, and resources within our Nucleic Acid Purification and Analysis Support Center.
Follow recommended DNA dilutions and leave the gel to cool down on the bench or for a few minutes in the fridge. Please check troubleshooting tips provided in the manual.
No. E-Gel agarose gels have enough buffering capacity for one run only. Performance will be impaired with multiple runs.