C.B.S. Scientific GCSGU-2640T-02 User Manual
Page 12
![background image](/manuals/555819/12/background.png)
www.cbsscientific.com
Horizontal Productivity Packages 9/2011
12
SECTION 4
Running Conditions
4.1 Recommended Power
As a rule, optimal resolution of larger molecules is achieved during longer runs at lower voltages,
whereas smaller molecules require shorter runs at higher voltages. Applied voltage gradients
can therefore be anywhere in the range of 1-10 VDC/cm of gel. Using the standard buffer
systems listed below, most runs will use 5 VDC/cm as a general rule.
The usual run time will vary for the voltage chosen but should range from 15 to 60 minutes.
Nucleic acid migration is monitored by the progress of marker dyes. Constant power is not a
necessity, but it produces uniform heat throughout the run, therefore minimizing band diffusion.
Be sure the polarity is correct i.e. that the DNA is loaded near the cathode (black electrode) to
run toward the anode (red terminal).
Agarose gels may be stored for several days at 4°C wrapped in plastic wrap. Seakem Agarose
(FMC) is used (normally) for preparative and analytical gels. Other types of agarose can be used
for special purposes.
4.2
Recommended Buffer and Agarose Volumes
Cat. #
Gel Bed dimensions
Buffer
(mls)
Agarose
for 1cm
thick slab
(mls)
GCSGU-014T-02
14cm x 20cm
1500
290
GCSGU-020T-02
20cm x 20cm
1850
400
GCSGU-030T-02
20cm x 30cm
1950
600
GCSGU-040T-02
20cm x 40cm
2050
800
GCSGU-2614T-02
26cm x 14cm
2200
400
GCSGU-2626T-02
26cm x 26cm
2600
700
GCSGU-2640T-02
26cm x 40cm
3400
1100
4.3 Recommended Buffers and Solutions*
Type
Concentrated Stock/liter
Final Concentration
TAE
50X - 242 gm Tris base
1X - 0.04M Tris-acetate
(Tris-acetate) 57.1ml glacial acetic acid
0.001M EDTA
100 ml 0.5M EDTA (pH 8.0)
TBE
5X - 54 gm Tris base
0.5X - 0.045M Tris-borate
(Tris-borate)
27.5 gm boric acid
0.001M EDTA
20 ml 0.5M EDTA (pH 8.0)
10X - Loading Buffer (DNA)*
0.25% Bromophenol blue
0.25% Xylene cyanol
20% Ficoll Type 400
0.1M EDTA, pH 8.0
Ethidium Bromide Staining
EtBr can be premixed with buffers and agarose for use during
electrophoresis. Add to agarose only after temperature has fallen below 55°C. Gels
can also be stained after electrophoresis in a soaking tray. Use EtBr at a final
concentration of 0.1µg/ml from a 1mg/ml stock solution. Ethidium Bromide is a powerful
mutagen. ALWAYS wear gloves, eye protection and protective clothing. Dispose of
solutions in accordance with the safety regulations of your institution.