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6 maximum well/comb volumes, Rectangle combs for double wide mini-vertical, Rectangle combs for triple wide mini-vertical – C.B.S. Scientific MGV-216-33 User Manual

Page 13

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C.B.S. œ Scientific

Double & Triple Wide Mini-Vertical

13

3.6

Maximum Well/Comb Volumes

NOTE: To calculate sample well volume expressed in millimeters (mm) of height,
divide maximum volume by tooth depth.


Rectangle Combs for Double Wide Mini-Vertical

# of wells

Tooth width/mm

0.75mm thickness

volume per tooth

microliters (

μl)

1.0mm thickness
vloume per tooth

microliters (

μl)

1.5mm thickness
volume per tooth

microliters (

μl)

12 11

82.5

110

165

14 9.1

68.3

91

136.50

16 7.7

57.75

77

115.5

17 6.7

50.25

67

100.5

20

5.66 42.45 56.6 84.9

28 4

30

40

60

32 3.4

25.5

34

51

35

2.95 22.13 29.5 44.25

Overall length of comb: 15.87cm
Tooth depth: 10mm
Spacing between teeth: 12-20 wells = 2.3mm 28-35 wells = 1.5mm



Rectangle Combs for Triple Wide Mini-Vertical

# of wells

Tooth width/mm

0.75mm thickness

volume per tooth

microliters (

μl)

1.0mm thickness
vloume per tooth

microliters (

μl)

1.5mm thickness
volume per tooth

microliters (

μl)

31 5.8mm

43.50

58

87

34 6.05mm

45.38

60.50

90.75

50 4.05mm

30.38

40.50

60.75

60 3.18mm

28.35

31.80

47.70

63 2.95mm

22.13

29.50

44.25

102 2mm

15

20

30

Overall length of comb: 28.4cm
Tooth depth: 10mm
Spacing between teeth: 31-34 wells = 2.4mm 50-63 wells = 1.5mm

SECTION 4
Running Conditions

4.1 Recommended Power

Precise electrophoresis conditions will vary according to the number and type of gels
used, buffer conditions employed, power input, and the general goal of the experiment.
Refer to the reference section for in-depth discussions on practical and theoretical
approaches to protein gel electrophoresis.

Using standard SDS-PAGE buffer systems apply 1-10 VDC/cm of gel. If running two
gels in the dual units, keep the volts the same but double the mA. It is also true that if the
thickness of the gel increases, increase the mA proportionally.

At constant voltage, the proteins will migrate at a constant rate during electrophoresis
with adequate heating appropriate for denaturing gels. Increasing the voltage/mA (for a
single gel thickness and percentage) will speed mobility but increase the risk of
overheating.

The sample migration rate can be increased by raising the input power. This can be
done in the dual systems, which employ ‘active’ temperature control. The joule heating
generated by the higher power is offset by the cooling effect of the water between the
gels. Exact conditions should be determined empirically but should be at least in the
20% range.

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