V. SPECIFICATIONS
TABLE B: General specifications
Gel dimensions (w x l)
Upper buffer chamber
capacity
Lower buffer chamber
capacity
Total running buffer
Total buffer capacity
Current (mAmps), constant
Max. voltage (volts)
Time requirements
Sample capacity
VI. UNIT ASSEMBLY FOR CASTING AND RUNNING GELS
1. Turn over the casting base so that the four acrylic
positioning squares are on the top.
2. Place the upper buffer chamber on the casting base.
The precision-machined upper buffer chamber should
fit snugly over the four squares.
3. Loosen the wing nuts and slide the clamp bars
outward. Please note the nylon alignment pins. These
pins assure that the glass plates are properly placed
over the upper buffer chamber gasket, while the acrylic
squares on the casting base assure that the glass is
positioned evenly and at the proper place for optimum
sealing on the casting base gaskets.
4. Gel Plate assembly: On a clean, level bench position the
two side spacers flush with the edges of the blank glass
plate and overlay the notched plate.
Place the gel plate assemblies (cassettes) with the notched glass plate innermost against the gasket of
the upper buffer chamber. The assemblies should rest on the positioning squares of the casting base and
between the nylon alignment pins.
6
StarPhoresis 2-Gel Mini and Wide Mini Vertical Electrophoresis Systems
N2510-1010
N2516-1410
10 x 10cm
170ml
~ 240ml
~ 450ml
~ 450ml
15–35mA/Gel
15–50mA/Gel
600V
30–90 minutes
60–120 minutes
24
N2520-2010
16 x 14cm
20 x 20cm
400ml
~ 300ml
~ 800ml
~ 650ml
~ 1250ml
~ 650ml
~ 1250ml
15–75mA/Gel
600V
60–180 minutes
48
N2520-1010
20 x 10cm
600ml
400ml
~ 450ml
~ 750ml
1100–1300ml
30–45mA/Gel
600V
600V
30–90 minutes
50
72