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C.B.S. Scientific GCSGU-2640T-02 User Manual

Page 12

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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.



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