Title | Egel 1kb plus express ladder man |
---|---|
Course | Genetics |
Institution | Western Sydney University |
Pages | 3 |
File Size | 217.6 KB |
File Type | |
Total Downloads | 11 |
Total Views | 130 |
Download Egel 1kb plus express ladder man PDF
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Choosing the right DNA ladder for your E-Gel™ agarose gel Agarose %
E-Gel™ Single Comb
E-Gel™ 50 bp DNA Ladder
E-Gel™ 1 Kb Plus DNA Ladder Cat. No. 10488090
E-Gel™ 1 Kb Plus Express DNA Ladder Cat. No. 10488091
E-Gel™ Sizing DNA Ladder Cat. No. 10488100
E-Gel™ Low Range Quantitative DNA Ladder Cat. No. 12373031
E-Gel™ 96 High Range DNA Marker
Cat. No. 10488096
Cat. No. 10488099
1%
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2%
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4%
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1.2%
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2%
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—
0.8%
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1.2%
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2%
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4%
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—
E-Gel™ EX
E-Gel™ with SYBR™ Safe
E-Gel™ Ultra Low Range DNA Ladder
Cat. No. 12352019
1%
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2%
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—
E-Gel™ CloneWell™ II
0.8%
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—
—
E-Gel™ SizeSelect™ II
2%
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—
—
0.8%
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—
—
1%
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—
—
2%
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—
—
1%
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—
E-Gel™ Double Comb
E-Gel™ NGS ™
E-Gel Go!
E-Gel™ 48
E-Gel™ 96 E-Gel™ 96 SYBR™ Safe
2%
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4%
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1%
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2%
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1%
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Recommended DNA ladder
Compatible DNA ladder
Print Options
Gel type
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Prepare and load DNA ladders and samples This protocol provides a brief description of how to use the DNA ladder with E-Gel™ agarose gels. For detailed instructions on using specific types of E-Gel™ agarose gels, go to thermofisher.com or contact Technical Support.
Step
Action a. Thaw, mix and briefly centrifuge DNA ladder before use. b. Prepare DNA ladder.
1
2
Prepare DNA ladder
Prepare samples
∤ ∤ ∤ ∤
For E-Gel™ CloneWell™ II Agarose Gels, mix and use 25 µL of the ladder without dilution. For E-Gel™ EX Agarose Gels, mix 2 µL of DNA ladder with 18 µL of water. For E-Gel™ Agarose Gels, mix and use the ladder without dilution. For E-Gel™ 48 Agarose Gels, mix 2 µL of DNA ladder with 13 µL of water.
a. Dilute your sample 2- to 10-fold with TE Buffer (Cat. No. AM9858), 1X E-Gel™ Sample Loading Buffer (Cat No. 10482055), or water. b. Mix gently. a. Load DNA ladders and DNA samples into the appropriate wells of the E-Gel™ agarose gel.
∤ 3
Load samples and DNA ladders
Add 25 µL for E-Gel™ CloneWell™ II Agarose Gels. Note: All wells of E-Gel™ Clonewell™ II Agarose Gels must be pre-filled with 50 µL of water.
∤ ∤
Add 20 µL for E-Gel™ and E-Gel™ EX Agarose Gels. Add 15 µL for E-Gel™ 48 Agarose Gels.
b. Add water to any empty wells, so that all wells contain an equal volume of liquid. c. Proceed to Perform electrophoresis of E-Gel™ agarose gel.
For support, visit thermofisher.com/support. 3 September 2017
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Perform electrophoresis of E-Gel™ agarose gel This protocol provides a brief description of how to perform electrophoresis with E-Gel™ agarose gels. For detailed instructions on using specific types of E-Gel™ agarose gels, go to thermofisher.com or contact Technical Support.
Step
Action ™
a. Choose the appropriate E-Gel run protocol for your gel type based on the electrophoresis device being used. Gel type Program E-Gel™ Power Snap Electrophoresis Device (Cat. No. G8100)
4
Perform electrophoresis
E-Gel™ Clonewell™ II Agarose Gel (0.8%) E-Gel™ EX Agarose Gel (1%, 2%)
Recommended run time
CloneWell 0.8%
12 min (40 min max)
E-Gel EX 1-2%
10 min (20 min max)
E-Gel 0.8-2%
26 min (40 min max)
E-Gel™ Agarose Gel (0.8%, 1.2%, 2%) E-Gel™ Double Comb Agarose Gel (1%, 2%) E-Gel™ E-Base™ Device E-Gel™ 48 Agarose Gel (1%, 2%)
E-Gel Double Comb
13 min (20 min max)
EG
20 min
b. Run the program to start electrophoresis. Visualize DNA ladder and samples.
the E-Gel Power Snap Camera (Cat. No. G8200), E-Gel Imager (Cat. No. · Use 466612), or other blue light imager to detect DNA bands stained with SYBR ™
5
Visualize agarose gel
™
™
stains.
· UV transilluminator to detect DNA bands stained with ethidium bromide.
For support, visit thermofisher.com/support. 3 September 2017
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