Auto2D^® Automated 2-D Gel Electrophoresis Device Protocol

The Auto2D^® 2-D Electrophoresis Device is user-friendly and enables two-dimensional electrophoresis in 1-2 hours for faster, more reproducible results.

• Auto2D^® Device Workflow
• Auto2D^® Device Reagent Preparation
• Auto2D^® Device Sample Preparation
• Powering on the Auto2D^® Device
• Auto2D^® Device Chip Assembly

Auto2D^® Device Workflow

The Auto2D^® Electrophoresis Device fully automates the process of 2-D electrophoresis, separating proteins first by isoelectric point and second by molecular weight. Complete protein separation is achieved in just over one hour.

Sample Preparation

Application of Reagents

Gel Rehydration

3 Minutes

Sample Loading to Gel

10 Minutes

First Dimension: Isoelectric Focusing

17 Minutes

SDS Equilibration

3 Minutes

Second Dimension: SDS-PAGE

33 Minutes

Detection

Auto2D^® Device Reagent Preparation

1. Prepare and store Reagent Kits as directed in the literature provided with the kits, or the complete User Guide (online).
2. Allow the following products stored at low temperatures to equilibrate to room temperature (20-25 °C approximately 10 minutes).
   • IEF Chip
   • PAGE Chip
   • Rehydration Solution
   • DTT Solution
   • Ampholyte
3. Prepare Working Rehydration Solution for rehydration of IEF Chip and extraction/dilution of protein sample:

Reagents	Volume	Final Concentration
Rehydration Solution	189 μL
DTT Solution (1M)	10 μL	50 mM
Ampholyte*	1-2 μL	0.5-1% v/v
Total	200 μL

*Select ampholyte according to the range of IEF Chip to use. For ampholytes at 40% stock concentration, add 1 μL. For ampholytes at 100X, add 2 μL.

4. Prepare Working Equilibration Buffer for equilibration of focused proteins before SDS-PAGE.

Reagents	Volume	Final Concentration
Equilibration buffer premix	760 μL
DTT Solution (1M)	40 μL	50 mM
Total	800 μL

Auto2D^® Device Sample Preparation

Dissolve the protein sample in the Working Rehydration Solution, prepared according to step 3. Sample may be diluted 2-fold or more with Working Rehydration Solution to reach desired protein concentration and decrease salt concentration.

A high salt concentration can affect protein separation during isoelectric focusing and cause the current to exceed 100 μA. Samples with a high salt concentration should be desalted by either:

• TCA/ acetone precipitation and resuspension of proteins in working rehydration solution
  OR
• Buffer exchange using a spin column
  OR
• Desalting protocol using Auto2D^® Device (See complete User Guide online, for more information.)

Note: During protein resuspension, avoid heating proteins over 37 °C.

Quantify proteins. Between 0.1 - 100 μg of protein can be loaded for 2D electrophoresis. The optimum amount of protein will depend on detection method and sample complexity. The following protein amounts should be used as a starting point, users may need to optimize the loading amount for their particular sample.

• Coomassie^® Brilliant Blue staining: 50 μg
• Fluorescent staining: 10 μg
• Silver staining: 5 μg
• Fluorescent pre-labeling: 3 μg

Use the amount of protein loaded into Solution Chip to determine whether to use S, M, or L recipe type for protein separation.

The sample volume applied to the device is 13 - 15 μL. Sample can be diluted with Working Rehydration Solution, as necessary.

Powering on the Auto2D^® Device

Select the appropriate power cord (provided with the device) that is compatible with the power outlets in your country. Firmly push the matching end into the back of the Auto2D^® Device, and the other end into the power outlet.

The power switch is located next to the AC plug port on the back of the Auto2D^® Device. Press the switch up to turn on.

The application will be automatically launched. From the screen, select Auto2D^® Plus mode.

Load a Recipe

Choose SETTING > RECIPE. Touch the Recipe Information screen. Recipe select dialog box will appear.

Select “RECIPE NAME” > LOAD > OK > EXIT.

Note: Confirm the desired Recipe name is displayed on the upper right side of the screen.

Auto2D^® Device Chip Assembly

1. Remove the white tape on the anode side of the Chip.
2. Carefully remove the plastic cover on the cathode side of the Chip.
3. Gently rinse anode and cathode buffer wells with distilled water. Using a paper cleaning wipe, carefully wipe any liquid from the top of the Chip making sure not to damage the thin strip of gel located on the Cathode side of the Chip.

Insert the Chips Into the Tray

On the Auto2D^® Device touch screen, Choose OPEN > OK.

Once tray is open, place the PAGE Chip (light blue line) with the anode side in front. Place the Solution Chip Plus (dark blue lines) on top of the PAGE Chip with the cut-off corners in the front.

Apply the Solutions

1. Cathode Buffer, 4500 μL
2. Distilled Water, 4500 μL
3. Anode Buffer, 4000 μL
4. Working Equilibration Buffer:
   • 700 μL
   • 700 μL (optional)
5. Working Rehydration Solution, 100 μL
6. Sample, 13 – 15 μL
7. Filter Paper and Water* 5 μL, each

*Wetted filter paper can be used as a wick to trap salt. Using filter paper is recommended to enhance separation of protein samples containing a high salt concentration when using Auto2D^® Plus programs and is required when using Auto2D^® Desalting program. Filter paper should be 0.2 – 0.3 mm in thickness and cut to a size of 8 mm x 4 mm.

Placement of the Electrode Chip Plus

Position the ▼ towards the front.

IEF Chip

Remove the IEF Chip protective film.

Insert the IEF Chip in the slot indicated by the white dot on the Electrode Chip Plus.

Before the Starting Electrophoresis step, verify the following:

• Electrode Chip Plus is not wet except for anode and cathode chamber.
• The clear cover on the cathode side of the PAGE Chip is removed.
• Solution has been added where required.

Start Electrophoresis

Choose CLOSE > OK > START > OK.

Electrophoresis will begin.

After Electrophoresis

Remove the Gel

Choose OK > OPEN > OK.

1. Remove and dispose of the IEF Chip and remaining solutions in the Solution Chip Plus. See Disposal section.
2. Remove the PAGE Chip and rinse with distilled water.
3. Open the cassette with spatula.

4. Mark the orientation of the gel by making a small cut in one of the corners. This will help you to locate the alkaline and acidic sides and high-low molecular weight in your gel (see below).

Clean Up

Clean the Electrode Chip Plus with distilled water immediately and let it air dry after use.

Power Off

Choose MENU > EXIT APPLICATION > OK > SYSTEM/OS SHUT DOWN > OK

Turn off switch on the back of the device.

Note: If condensation is observed inside the device, leave the tray open for a while before turning off the power, to allow the inside to dry.

Disposal

Components exposed to samples should be disposed of with biological waste. Other materials should be disposed of according to all applicable international, federal, state, and local regulations. Refer to the components’ Safety Data Sheet for hazard information.

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