Cleaver Scientific multiSUB MSMINI User manual

Version 1
multiSUB® Electrophoresis Systems
MSMINI MSMIDI MSCHOICE MSCHOICEST MSMAXI
Instruction Manual
Catalogue No: MSMINI7, MSMINI10, MSMINIDUO
MSMIDI7, MSMIDI10, MSMIDIDUO
MSCHOICE7, MSCHOICE10, MSCHOICE15, MSCHOICETRIO
MSCHOICEST20, MSCHOICEST25
MSMAXI10, MSMAXI15, MSMAXI20, MSMAXIDUO, MSMAXI25

Page 2
Table of Contents
Page
Section 1 Safety Information 3
1.1 Safety Precaution 3
Section 2 General Information 4
2.1 Packing Lists 4
2.2 Care and Maintenance 7
Section 3 Operating Instructions 8
3.1 Usage Guidance and restrictions 8
3.2 Setting up the Horizontal Gel Tanks 9
3.3 Gel Preparation 10
3.4 Gel Pouring 11
3.5 Running the Gel 13
3.6 Gel Staining and Viewing 14
3.7 Solutions 14
Section 4 References 15
Section 5 Trouble Shooting Guide 16
Section 6 Product Information 17
6.1 Catalogue numbers and product descriptions for multiSUB® units & accessories 17
6.2 Combs 19
6.3 Catalogue numbers and product descriptions for CSL Related Products 21
Section 7 Warranty 22

Page 3
Section 1 Safety Information
1.1 Safety Precaution
When used correctly, these units pose no health risk. However, these units can deliver dangerous levels of
electricity and are to be operated only by qualified personnel following the guidelines laid out in this
instruction manual. Anyone intending to use this equipment should read the complete manual thoroughly.
The unit must never be used without the safety lid correctly in position. The unit should not be used if there is
any sign of damage to the external tank or lid.
These units comply with the following European directives:
2006/95/CE Low Voltage Directive and 2014/30/UE (official Title 2004/108/EC) EMC Electromagnetic
Compatibility
By virtue of the following harmonised standards:
BS EN IEC 61010-1: 2010 Safety Testing of Lab Equipment
BS EN IEC 61326-1:2013 EMC Electro Magnetic Compatibility

Page 4
Section 2 General Information
2.1 Packing Lists
MSMINI7, MSMINI10, MSMINIDUO
Units include tank, lid and electrodes and include the following accessories:
Tray
Tray Dams
Combs
Loading Guides
Cables
MSMINI7
MS7-UV7
7 x 7cm (W x L)
MS7-UVDAM
Pack of 2
2 x MS7-8-1
1mm, 8
sample
MS7-LG –Strips
MS7-WP –
Platform
CSL-CAB
MSMINI10
MS7-UV10
7 x 10cm (W x
L)
MS7-UVDAM
Pack of 2
2 x MS7-8-1
1mm, 8
sample
MS7-LG –Strips
MS7-WP –
Platform
CSL-CAB
MSMINIDUO
MS7-UV7
MS7-UV10
MS7-UVDAM
Pack of 2
2 x MS7-8-1
1mm, 8
sample
MS7-LG –Strips
MS7-WP –
Platform
CSL-CAB
MSMIDI7, MSMIDI10, MSMIDIDUO
Units include tank, lid and electrodes and include the following accessories:
Tray
Tray Dams
Combs
Loading Guides
Cables
MSMIDI7
MS10-UV7
10 x 7cm (W x
L)
MS10-
UVDAM
Pack of 2
2 x MS10-16-1
1mm, 16
sample
MS10-LG –Strips
MS10-WP –
Platform
CSL-CAB
MSMIDI10
MS10-UV10
10 x 10cm (W
x L)
MS10-
UVDAM
Pack of 2
2 x MS10-16-1
1mm, 16
sample
MS10-LG –Strips
MS10-WP –
Platform
CSL-CAB
MSMIDIDUO
MS10-UV7
MS10-UV10
MS10-
UVDAM
Pack of 2
2 x MS10-16-1
1mm, 16
sample
MS10-LG –Strips
MS10-WP –
Platform
CSL-CAB

Page 5
MSCHOICE7, MSCHOICE10, MSCHOICE15, MSCHOICETRIO
Units include tank, lid and electrodes and include the following accessories:
Tray
Tray Dams
Combs
Loading Guides
Cables
MSCHOICE7
MS15-UV7
15 x 7cm
(W x L)
MS15-
UVDAM
Pack of 2
2 x MS15-20-
1
1mm, 20
sample
MS15-LG –
Strips
MS15-WP –
Platform
CSL-CAB
MSCHOICE10
MS15-UV10
15 x 10cm
(W x L)
MS15-
UVDAM
Pack of 2
2 x MS15-20-
1
1mm, 20
sample
MS15-LG –
Strips
MS15-WP –
Platform
CSL-CAB
MSCHOICE15
MS15-UV15
15 x 15cm
(W x L)
MS15-
UVDAM
Pack of 2
2 x MS15-20-
1
1mm, 20
sample
MS15-LG –
Strips
MS15-WP –
Platform
CSL-CAB
MSCHOICETRIO
MS15-UV7
MS15-UV10
MS15-UV15
MS15-
UVDAM
Pack of 2
2 x MS15-20-
1
1mm, 20
sample
MS15-LG –
Strips
MS15-WP –
Platform
CSL-CAB
MSCHOICEST20, MSCHOICEST25
Units include tank, lid and electrodes and include the following accessories:
Tray
Tray
Dams
Combs
Loading Guides
Cables
MSCHOICEST20
MS15-
UVST20 15 x
20 cm
(W x L)
MS15-
UVDAM
Pack of 2
4 x MS15-
28MC-1
1mm thick, 28
sample MC
MS15-LG –
Strips
MS15-WP –
Platform
CSL-CAB
MSCHOICEST25
MS15-
UVST25 15 x
25 cm
(W x L)
MS15-
UVDAM
Pack of 2
4 x MS15-
28MC-1
1mm thick, 28
sample MC
MS15-LG –
Strips
MS15-WP –
Platform
CSL-CAB

Page 6
MSMAXI10, MSMAXI15, MSMAXI20, MSMAXIDUO, MSMAXI25
Units include tank, lid and electrodes and include the following accessories:
Tray
Tray
Dams
Combs
Loading Guides
Cables
MSMAXI10
MS20-UV10
20 x 10cm (W x
L)
MS20-
UVDAM
Pack of 2
2 x MS20-20-
1
1mm, 20
sample
MS20-LG –Strips
MS20-WP –
Platform
CSL-CAB
MSMAX15
MS20-UV15
20 x 15cm (W x
L)
MS20-
UVDAM
Pack of 2
2 x MS20-20-
1
1mm, 20
sample
MS20-LG –Strips
MS20-WP –
Platform
CSL-CAB
MSMAXI20
MS20-UV20
20 x 20cm (W x
L)
MS20-
UVDAM
Pack of 2
2 x MS20-20-
1
1mm, 20
sample
MS20-LG –Strips
MS20-WP –
Platform
CSL-CAB
MSMAXIDUO
MS20-UV10
MS20-UV20
MS20-
UVDAM
Pack of 2
2 x MS20-20-
1
1mm, 20
sample
MS20-LG –Strips
MS20-WP –
Platform
CSL-CAB
MSMAXI25
MS20-UV25
20 x 25cm (W x
L)
MS20-
UVDAM
Pack of 2
2 x MS20-20-
1
1mm, 20
sample
MS20-LG –Strips
MS20-WP –
Platform
CSL-CAB
Packing list checked by ________________________ Date ____________
The packing lists should be referred to as soon as the units are received to ensure that all components have
been included. The unit should be checked for damage when received.
Please contact your supplier if there are any problems or missing items.

Page 7
2.2 Care and Maintenance
Cleaning Horizontal Units
Units are best cleaned using warm water and a mild detergent. Water at temperatures above 600C can cause
damage to the unit and components.
The tank should be thoroughly rinsed with warm water or distilled water to prevent buildup of salts but care
should be taken not to damage the enclosed electrode and vigorous cleaning is not necessary or advised.
Air drying is preferably before use.
The units should only be cleaned with the following:
Warm water with a mild concentration of soap or other mild detergent.
Compatible detergents include dishwashing liquid, Hexane and Aliphatic hydrocarbons
The units should not be left to in detergents for more than 30 minutes.
The units should never come into contact with the following cleaning agents, these will cause irreversible
and accumulative damage:
Acetone, Phenol, Chloroform, Carbon tetrachloride, Methanol, Ethanol, Isopropyl alcohol
Alkalis.
Rnase Decontamination
This can be performed using the following protocol:
Clean the units with a mild detergent as described above.
Wash with 3% hydrogen peroxide (H2O2) for 10 minutes.
Rinsed with 0.1% DEPC- (diethyl pyro carbonate) treated distilled water,
Caution: DEPC is a suspected carcinogen. Always take the necessary precautions when using.
RNaseZAP™ (Ambion) can also be used. Please consult the instructions for use with acrylic gel tanks.

Page 8
Section 3 Operating Instructions
Further information (including videos) regarding setting up and running the multiSUB® units can be found at
www.cleaverscientific.com
3.1 Usage Guidance and restrictions
• Maximum altitude 2,000m.
•Temperature range between 4°C and 65°C.
• Maximum relative humidity 80% for temperatures up to 31OC decreasing linearly to 50% relative humidity at
40OC.
• Not for outdoor Use.
This apparatus is rated POLLUTION DEGREE 2 in accordance with IEC 664.
POLLUTION DEGREE 2, states that: “Normally only non-conductive pollution occurs.
Occasionally, however, a temporary conductivity caused by condensation must be expected”.

Page 9
3.2 Setting up the Horizontal Gel Tanks
Instructions for fitting Electrode Cables
1. Note the position of the lid on the unit. This shows the correct polarity and the correct orientation of the
cables, black is negative and red positive.
2. Remove the lid from the unit. Note if the lid is not removed, fitting the cables may result in un-tightening
of the gold plug and damage to the electrode.
3. Screw the cables into the tapped holes as fully as possible so that there is no gap between the lid and the
leading edge of the cable fitting.
4. Refit the lid.
Instructions for fitting Loading Guides
These can be fitted to enhance visibility of the wells if desired. They can be fitted to the white vinyl platform
sheet or to the unit itself.
1. Seat the tray in the unit and note the position of the comb grooves. The samples run black to red but the
trays can be used frontward or backwards so ensure that the comb grooves closest to the black electrode
are marked.
2. Remove the tray.
3. Peel the back off of the loading guide and carefully apply the loading guide directly to the gel platform.
The unit is now ready to be used.

Page 10
3.3 Gel Preparation
1. Table 1 below shows the volume of agarose solution required to make the desired agarose gel for each unit
tray size. For a standard 0.7% agarose gel, add 0.7 grams of agarose to 100 ml of 1x TAE or TBE solution.
The same 1 x solution should be used in the tank buffer solution.
Table 1
multiSUB® Mini
Tray
7 x 7 cm
7 x 10 cm
Gel volume for a 5mm thick gel
25 mL
35 mL
multiSUB® Midi
Tray
10 x 7 cm
10 x 10 cm
Gel volume for a 5mm thick gel
35 mL
50 mL
multiSUB® Choice
Tray
15 x 7 cm
15 x 10 cm
15 x 15 cm
Gel volume for a 5mm thick gel
52.5 mL
75 mL
112.5 mL
multiSUB® Choice
STRETCH
Tray
15 x 20 cm
15 x 25 cm
Gel volume for a 5mm thick gel
150 mL
187.5 mL
multiSUB® Maxi
Tray
20 x 10 cm
20 x 15 cm
20 x 20 cm
Gel volume for a 5mm thick gel
100 mL
150 mL
200 mL
2. Add the agarose powder to a conical flask.
3. Add the appropriate amount of 1x TAE or TBE solution from the table above. To prevent evaporation during
the dissolving steps below, the conical flask should be covered with parafilm.
4. Dissolve the agarose powder by heating the agarose either on a magnetic hot plate with stirring bar or in a
microwave oven. If using the microwave method, the microwave should be set at around a 400 watt or
medium setting and the flask swirled every minute. The solution should be heated until all crystals are
dissolved. This is best viewed against a light background. Crystals appear as translucent crystals. These will
interfere with sample migration if not completely dissolved.
The gel must be cooled to between 50°C and 60°C degrees before pouring.

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3.4 Gel Pouring
The CSL Multi sub range of units allows three different methods of gel casting:
Casting Dams
Flexicaster
Traditional Tape
Using trays with Casting Dams
1. To fit the casting dams, place one casting dam on the bench with the groove facing upwards (see figure 1).
Push the edge of the tray down firmly into the groove (see figure 2). Repeat this for the other side (figure
3). The dams should be fitted so that there is no gap between the sides of the tray and the groove in the
dams. This will ensure that there is no possibility of gel leakage.
2. Place the comb(s) in the grooves. Each tray has more than one comb grove so that multiple combs can be
used. Using multiple combs increases sample number available per gel but decreases run length and care
must be taken to ensure that samples from the first wells do not migrate into the lanes of the second
comb wells.
3. Pour in the agarose carefully so as not to generate bubbles. Any bubbles that do occur can be smoothed to
the edge of the gel and dispersed using a pipette tip.
4. Allow the agarose to set, ensuring that the gel remains undisturbed.
5. Carefully remove the gel casting gates and comb and transfer the gel including tray to the main tank.
Figures 1 –3 Assembling the casting dam to the tray
Figure 1 Figure 2 Figure 3

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Using The Flexicaster
See figures 4 and 5 for Flexicaster MS7-FC and MS20-FC
1. Level the Flexicaster base by adjusting the feet so that the bubble is exactly central.
2. Insert the desired length tray into the Flexicaster such that one end of the tray is pushed up and seals
against the silicone mat of the permanent end of the Flexicaster.
3. Position the movable end of the Flexicaster so that the silicone mat is pushed against the other end of the
tray.
4. Turn the cam so that the silicone mat tightly seals against the side of the tray. Pour in the agarose carefully
so as not to generate bubbles. Any bubbles that do occur can be smoothed to the edge of the gel and
dispersed using a pipette tip.
5. Allow the agarose to set, ensuring that the gel remains undisturbed.
6. Carefully remove the gel casting gates and comb and transfer the gel including tray to the main tank.
Figure 4 MS7-FC Figure 5 MS20-FC
Using Traditional tape method
1. Autoclave or plastic backed general tape should be used. A length 5cm longer than the width of each end
of the tray should be cut. One length should be placed over one end of the tray and stuck m1cm in from
the tray edge. This should then be folded and the edges sealed securely. Repeat for the other end and
place onto a level surface for gel pouring.
2. Place the comb(s) in the grooves. Each tray has more than one comb grove so that multiple combs can be
used. Using multiple combs increases sample number available per gel but decreases run length and care

Page 13
must be taken to ensure that samples from the first wells do not migrate into the lanes of the second
comb wells.
3. Pour in the agarose carefully so as not to generate bubbles. Any bubbles that do occur can be smoothed to
the edge of the gel and dispersed using a pipette tip.
4. Allow the agarose to set, ensuring that the gel remains undisturbed.
5. Carefully remove the gel casting gates and comb and transfer the gel including tray to the main tank.
3.5 Running the Gel
1. Mix the sample to be loaded with sample buffer –see solutions for common sample buffers. Usually 3ul
of sample buffer is adequate but less may be used with sample volumes of less than 10ul.
2. Fill the unit with buffer until the gel is just flooded with buffer. This will give the fastest resolution times.
For enhanced quality of resolution of sample, fill the unit to 5mm above the gel.
3. Load the samples into the wells using pipettes. Multi-channel pipettes can be used for loading samples
with MC compatible combs, see listing in accessories for identification of these.
4. Carefully place the lid on the tank and connect to a power supply.
5. Typically gels are run at between 90 and 150 volts. However, maximum voltages are indicated on the
serial badge of each unit. It should be noted that higher voltages generally give faster but poorer quality
sample resolution.

Page 14
3.6 Gel Staining and Viewing
The Multi Sub trays allow staining to be performed without removing the gel from the tray if this is preferred.
1. Transfer the gel to a vessel containing the appropriate volume of 0.5 µg/ml ethidium bromide stain for 15–
30 minutes, see solutions for stock stain concentration and adjust to the volume used accordingly. The
entire gel should be covered.
NOTE: Ethidium bromide is a suspected carcinogen and the necessary safety precautions should be
undertaken.
2. De-stain the gel for 10–30 minutes in distilled water again ensuring the gel is completely immersed.
3. Rinse the gel twice for a couple of seconds with distilled water.
4. Transfer the gel to a UV Transilluminator.
5. The samples will often appear as brighter, clearer bands when photographed or viewed using a gel
documentation system. However if the gel bands are too faint then the staining procedure should be
adjusted so that there is less de-staining. If there is too much background then the staining procedure
should be adjusted so that there is more de-staining.
3.7 Solutions
1x TAE 40 mM tris (pH 7.6), 20 mM acetic acid, 1 mM EDTA.
50x (1L) dissolve in 750 ml distilled water:
242 g tris base (FW = 121)
57.1 ml glacial acetic acid
100 ml 0.5 M EDTA (pH 8.0).
Fill to 1 litre with distilled water.

Page 15
1x TBE 89 mM tris (pH 7.6), 89 mM boric acid, 2 mM EDTA
10x (1L) dissolve in 750 ml distilled water:
108 g tris base (FW = 121)
55 g boric acid (FW = 61.8)
40 ml 0.5 M EDTA (pH 8.0)
Fill to 1 litre with distilled water.
Sample Loading Dye
10x sample buffer stock consists of 50% glycerol, 0.25% bromophenol blue, and
0.25% xylene cyanole FF in 1x TAE buffer. Only 1–10 ml of the 10x loading dye should be prepared.
Ethidium Bromide Solution
Add 10 mg of Ethidium Bromide to 1 ml distilled water.
Section 4 References
1. Sambrook, Fritsch, and Maniatis, Molecular Cloning A Laboratory Manual, Second Edition, Cold Spring
Harbor Laboratory Press, 1989.
2. Current Protocols in Molecular Biology, Greene Publishing Associates and Wiley-Interscience, 1989.

Page 16
Section 5 Troubleshooting Guide
Problem
Cause
Solution
Bands sharp but not enough bands
seen
Gel agarose percentage too high
Incomplete digestion
Decrease agarose percentage.
Review enzyme activity, digest
further.
Band smearing and streaking
Agarose has improper endosmosis
Salt concentration in sample too high
Excessive power and heating
Sample spilled out of well
Incomplete digestion, nuclease
contamination, bad enzyme
Sample wells cast through the gel.
Sample leaks along bottom of
running surface
Consult Cleaver Scientific about
agarose.
Reduce salt concentration to ≤0.1M.
Reduce voltage. See electrophoresis
instructions.
Apply sample carefully. Increase gel
thickness for large sample volumes.
Adjust comb height.
Heat sample. Review enzyme
activity. Digest sample further.
Comb should be placed to 1 to 2 mm
above the base of the running
surface.
Curved line or distortion of bands
Bubbles in sample wells
Remove bubbles prior to
electrophoresis.
Curved bands, smiles
Sample overload
Reduce load.
Differential relative mobilities
Sample spilled out of wells
Unit not leveled
Samples should have proper density.
Apply carefully.
Level unit. Use a steady work bench.
Gels crack
Too high voltage gradient, especially
with low melting temperature
agarose or low gel strength gels
Reduce voltage. Run gel at lower
temperature.
High MW bands sharp; low MW
bands smeared
Gel agarose percentage too low
Increase agarose percentage. Switch
to polyacrylamide.
Ragged bands
Sample density incorrect
Sample well deformed
Excessive power or heating
See sample application instructions.
Carefully remove comb, especially
from soft gels. Make sure gel has
solidified.
Cooling soft gels aids in comb
removal.
Reduce voltage. See electrophoresis
instructions.
Slanted lanes (bands)
Gel not fully solidified
Comb warped or at an angle
Gel to solidify for at least 30-45min.
Check alignment of comb.

Page 17
Section 6 Product Information
6.1 Catalogue numbers and product descriptions for multiSUB® units & accessories
Catalogue No.
Product description
MSMINI7
multiSUB® Mini, 7 x 7cm UV Tray, 2 x 8 sample combs, loading guides and dams
MSMINI10
multiSUB® Mini, 7 x 10cm UV Tray, 2 x 8 sample combs, loading guides and dams
MSMINIDUO
multiSUB® Mini, 7 x 7cm & 7 x 10cm UV Tray, 2 x 8 sample combs, loading guides and dams
MS7-UV7
7 x 7cm UV Tray
MS7-UV10
7 x 10cm UV Tray
MS7-PE
Positive Electrode
MS7-NE
Negative Electrode
MS7-UVDAM
Casting Dams
MS7/10-FC
multiSUB® Mini/Midi Flexi caster
MS7-LG
Adhesive Loading Guides
MS7-WP
Viewing Platform
MSMINICP
Cool-pack and Platform
MSMINIBSB
Buffer Saver Blocks, pk/2 saves 100ml of buffer
MS7-UVS
7cm UV Gel Scoop
CSL-CAB
Electrophoresis cable (Black & Red)
MSMIDI7
multiSUB® Midi, 10 x 7cm UV Tray, 2 x 16 sample combs, loading guides and dams
MSMIDI10
multiSUB® Midi, 10 x 10cm UV Tray, 2 x 16 sample combs, loading guides and dams
MSMIDIDUO
multiSUB® Midi, 10 x 7cm & 10 x 10cm UV Tray, 2 x 16 sample combs, loading guides and dams
MS10-UV7
10 x 7cm UV Tray
MS10-UV10
10 x 10cm UV Tray
MS10-PE
Positive Electrode
MS10-NE
Negative Electrode
MS10-UVDAM
Casting Dams
MS7/10-FC
multiSUB® Mini/Midi Flexi caster
MS10-LG
Adhesive Loading Guides
MS10-WP
Viewing Platform
MSMIDICP
Cool-pack and Platform
MSMIDIBSB
Buffer Saver Blocks, pk/2 saves 100ml of buffer
MS10-UVS
10cm UV Gel Scoop
CSL-CAB
Electrophoresis cable (Black & Red)

Page 18
MSCHOICE7
multiSUB® ™ Choice 15 x 7cm UV Tray, 2 x 20 sample combs, loading guides and dams
MSCHOICE10
multiSUB® ™ Choice 15 x 10cm UV Tray, 2 x 20 sample combs, loading guides and dams
MSCHOICE15
multiSUB® ™ Choice 15 x 15cm UV Tray, 2 x 20 sample combs, loading guides and dams
MSCHOICETRIO
multiSUB® ™ Choice Trio 15 x 7,10 & 15cm UV Tray, 2 x 20 sample
combs, loading guides and dams
MSCHOICETRIO15
multiSUB® ™ Choice Trio 15 3 x 15cm UV tray, 2x 20 sample combs,
loading guides and dams
MSCHOICEST20
multiSUB® ™ Choice Stretch 20 15 x 20cm UV tray, 4 x 28 sample combs, loading guides and dams
MSCHOICEST25
multiSUB® ™ Choice Stretch 25 15 x 25cm UV tray, 4 x 28 sample combs, loading guides and dams
MS15-UV7
15 x 7cm UV Tray
MS15-UV10
15 x 10cm UV Tray
MS15-UV15
15 x 15cm UV Tray
MS15-UVST20
15 x 20cm UV Tray
MS15-UVS
15cm UV Gel Scoop
MS15-UVDAM
Casting Dams
MS15-PE
Positive Electrode
MS15-NE
Negative Electrode
MSMS15-LG
Adhesive Loading Guides
MS15-WP
Viewing Platform
MSCHOICECP
Cool-Pack and Platform
MS15/20-FC
multiSUB® Choice/ Maxi Flexi caster
MSMAXI10
20 x 10cm UV Tray, 2 x 20 sample, 1mm thick combs, casting dams, loading guides
MSMAXI15
20 x 15cm UV Tray, 2 x 20 sample, 1mm thick combs, casting dams, loading guides
MSMAXI20
20 x 20cm UV Tray, 2 x 20 sample, 1mm thick combs, casting dams, loading guides
MSMAXIDUO
20 x 10 & 20 x 20cm UV Tray, 2 x 20 sample, 1mm thick combs, casting dams, loading guides
MSMAXI25
20 x 25cm UV Tray, 2 x 20 sample, 1mm thick combs, casting dams, loading guides
MS20-UV10
20 x 10cm UV Tray
MS20-UV15
20 x 15cm UV Tray
MS20-UV20
20 x 20cm UV Tray
MS20-UV25
20 x 25cm UV Tray
MS20-UVDAM
Casting Dams
MS15/20-FC
multiSUB Choice/Maxi Flexi caster
MS20-LG
Adhesive Loading Guides
MS20-WP
Viewing Platform
MS20-PE
Positive Electrode
MS20-NE
Negative Electrode
MS20-UVS
20cm UV Gel Scoop
MSMAXICP
Cool-Pack and Platform
MSMAXIBSB
Buffer Saver Blocks pk/2 saves 450ml of buffer

Page 19
6.2 Combs –MC Denotes Multi Channel Pipette compatible
multiSUB® Mini
0.75mm
multiSUB® Midi
0.75mm
multiSUB® Choice
0.75mm
Multi Sub Maxi
0.75mm
No. of
Samples
Part Number
No. of
Samples
Part Number
No. of
Samples
Part Number
No. of
Samples
Part Number
1
MS7-1-0.75
1
MS10-1-0.75
1
MS15-1-0.75
1
MS20-1-0.75
2
MS7-2-0.75
2
MS10-2-0.75
2
MS15-2-0.75
2
MS20-2-0.75
4
MS7-4-0.75
4
MS10-4-0.75
4
MS15-4-0.75
4
MS20-4-0.75
8
MS7-8MC-0.75
MS7-8-0.75
8
MS10-8-0.75
10
MS15-10-0.75
MS15-10MC-0.75
10
MS20-10-0.75
10
MS7-10-0.75
10
MS10MC-10-0.75
12
MS15-12-0.75
16
MS20-16-0.75
12
MS7-12-0.75
12
MS10-12-0.75
14
MS15-14MC-0.75
20
MS20-20MC-0.75
16
MS7-16-0.75
16
MS10-16-0.75
16
MS15-16-0.75
25
MS20-25-0.75
20
MS10-20MC-0.75
18
MS15-18MC-0.75
30
MS20-30-0.75
20
MS15-20-0.75
36
MS20-36-0.75
28
MS15-28MC-0.75
40
MS20-40MC-0.75
30
MS15-30-0.75
multiSUB® Mini
1mm
multiSUB® Midi
1mm
multiSUB® Choice
1mm
Multi Sub Maxi
1mm
No. of
Samples
Part Number
No. of
Samples
Part Number
No. of
Samples
Part Number
No. of
Samples
Part Number
1
MS7-1-1
1
MS10-1-1
1
MS15-1-1
1
MS20-1-1
2
MS7-2-1
2
MS10-2-1
2
MS15-2-1
2
MS20-2-1
4
MS7-4-1
4
MS10-4-1
4
MS15-4-1
4
MS20-4-1
8
MS7-8MC-1
MS7-8-1
8
MS10-8-1
10
MS15-10-1
MS15-10MC-1
10
MS20-10-1
10
MS7-10-1
10
MS10MC-10-1
12
MS15-12-1
16
MS20-16-1
12
MS7-12-1
12
MS10-12-1
14
MS15-14MC-1
20
MS20-20MC-1
16
MS7-16-1
16
MS10-16-1
16
MS15-16-1
25
MS20-25-1
20
MS10-20MC-1
18
MS15-18MC-1
30
MS20-30-1
20
MS15-20-1
36
MS20-36-1
28
MS15-28MC-1
40
MS20-40MC-1
30
MS15-30-1

Page 20
multiSUB® Mini
1.5mm
multiSUB® Midi
1.5mm
multiSUB® Choice
1.5mm
Multi Sub Maxi
1.5mm
No. of
Samples
Part Number
No. of
Samples
Part Number
No. of
Samples
Part Number
No. of
Samples
Part Number
1
MS7-1-1.5
1
MS10-1-1.5
1
MS15-1-1.5
1
MS20-1-1.5
2
MS7-2-1.5
2
MS10-2-1.5
2
MS15-2-1.5
2
MS20-2-1.5
4
MS7-4-1.5
4
MS10-4-1.5
4
MS15-4-1.5
4
MS20-4-1.5
8
MS7-8MC-1.5
MS7-8-1.5
8
MS10-8-1.5
10
MS15-10-1.5
MS15-10MC-1.5
10
MS20-10-1.5
10
MS7-10-1.5
10
MS10MC-10-1.5
12
MS15-12-1.5
16
MS20-16-1.5
12
MS7-12-1.5
12
MS10-12-1.5
14
MS15-14MC-1.5
20
MS20-20MC-1.5
16
MS7-16-1.5
16
MS10-16-1.5
16
MS15-16-1.5
25
MS20-25-1.5
20
MS10-20MC-1.5
18
MS15-18MC-1.5
30
MS20-30-1.5
20
MS15-20-1.5
36
MS20-36-1.5
28
MS15-28MC-1.5
40
MS20-40MC-1.5
30
MS15-30-1.5
multiSUB® Mini
2mm
multiSUB® Midi
2mm
multiSUB® Choice
2mm
Multi Sub Maxi
1.75mm
No. of
Samples
Part Number
No. of
Samples
Part Number
No. of
Samples
Part Number
No. of
Samples
Part Number
1
MS7-1-2
1
MS10-1-2
1
MS15-1-2
1
MS20-1-2
2
MS7-2-2
2
MS10-2-2
2
MS15-2-2
2
MS20-2-2
4
MS7-4-2
4
MS10-4-2
4
MS15-4-2
4
MS20-4-2
8
MS7-8MC-2
MS7-8-2
8
MS10-8-2
10
MS15-10-2
MS15-10MC-2
10
MS20-10-2
10
MS7-10-2
10
MS10MC-10-2
12
MS15-12-2
16
MS20-16-2
12
MS7-12-2
12
MS10-12-2
14
MS15-14MC-2
20
MS20-20MC-2
16
MS7-16-2
16
MS10-16-2
16
MS15-16-2
25
MS20-25-2
20
MS10-20MC-2
18
MS15-18MC-2
30
MS20-30-2
20
MS15-20-2
36
MS20-36-2
28
MS15-28MC-2
30
MS15-30-2