Initial start-up procedure

1. If necessary, boot up the laptop computer and login to the ONI account.
2. Double-click the NimOS icon on the desktop to launch the acquisition and analysis software.
   
3. Click the Acquire button in the top left and then click Connect to Microscope.
   
4. NimOS will open the dialogue box below asking you to check the stage before it connects to the device to prevent damage.
   
5. Push the interlock slider to the in position and lift the lid of the chamber to make sure the area around the stage is clear and that all samples have been removed. There should be two stacks of small disc magnets, one on either side of the stage. They are there to secure the specimen.
   
6. Click Confirm and Connect. There will be noise as the laser engine starts up and messages will appear in NimOS as the computer connects to the different components.
7. In the Temperature Control area on the left, set the Target Temperature to 31ºC or 37ºC and press the Enable Control button (the button says Disable Control once pressed). The Nanoimager operates at a temperature around 6 degrees warmer than ambient and the temperature control must be set slightly above that to maintain stability.
   
8. Once the temperature has stabilised the control can be disabled.

Putting a sample on the stage

1. Slide the magnets off the stage. DO NOT pluck them off as the strength of the magnet could damage the stage by pulling on it too hard.
   
2. Put a drop or two of immersion oil on the objective lens.
3. Place your sample on the stage so that the area you want to image is on top of the objective lens (e.g., coverslip mounted on a slide, or well of a chambered cover glass).

4. Drop the magnets into place on either side of the specimen so that it is held down onto the stage. There are several disc magnets, so the sample can be held down at several positions if necessary.
   
   
   

   There needs to be space for the magnets on either side of the specimen, so vessels like 35 mm dishes can’t be used with the magnets.

5. Once the specimen is in position, close the lid of the chamber and pull out the interlock slider, otherwise the imaging lasers won’t work.

Focusing on the specimen

1. The Nanoimager has no eyepieces so focusing must be done using a camera image. This can be done using sample fluorescence, but I’ve found that it is a lot easier to use the focus laser, which reflects at the glass/water interface of the specimen and forms an image of a spot on the focus camera. The Focus Camera view is on the left of the NimOS GUI. You will just see camera noise unless the focus laser is switched on.
   
   
   

   If the focus camera view is not visible, select Show Focus Camera View from the Instrument menu.

2. Click the Focus Laser button in the Light Control area on the right.
   
   
   

3. You will probably initially see a faint diffuse signal at the top of the focus camera view. This is what the camera view looks like when out of focus. Change the Z position in the Position Control area on the right-hand side of the screen until there is an image of a small laser spot in the focus camera view.
   

   I have found that I can get close to the correct focus by typing in the values below:

   1. For an ibidi μ-slide -300
   2. For the bead channel alignment slide 16

   
   

4. Users should try Z position -300 first and gradually increase the value (making it more positive) until the laser spot starts to come into focus. The correct position is when the laser spot is at its smallest and brightest.
5. You can prevent the focus drifting by locking it to the laser reflection position. Click the Set Focus Ref. button in Position Control. The Nanoimager will auto focus on the focus laser reflection. When the auto focus is complete, click the Z Lock button to prevent further drift.
   
6. Note that the fluorescence from your specimen will most likely be at a different height to the reflection of the focus laser. You should use the Z offset field to adjust the focus offset so your fluorescence is in focus.

Single colour dSTORM

The instructions below assume that the sample is stained with a far-red dye like Alexa 647.

Click View in the Acquisition Control area to get a live image from the acquisition camera. There are two images, which correspond to two simultaneous colour channels. For dSTORM using a far-red dye you only need Channel 1, so untick Channel 0 in the Image Display Options on the left. For dyes other than far-red you will need Channel 0.

The live image won’t show any fluorescence until you illuminate the sample with a laser. Change the percentage power in the Light Control area to 5 to 10%. You can either click on the spin buttons or type in a value and press the Return key. Click on the 640 button to illuminate the specimen.

Focus on your specimen. If you are using Z lock you may need to adjust the Z offset as explained in the section on focusing.

Turn off the laser so you don’t photo bleach the specimen.

The best way start acquiring data is to use multidimensional acquisition. Click the Multiple Acquisition Setup button under the focus camera view on the left. In the Acquisition tab, click Single, set imaging mode to Normal, specify the laser power, exposure/frequency and number of images. In Saving, specify the Dataset Tag, which will be the folder where the files are stored, and the Acquisition Tag, which will be the filename. Note that the date will be automatically included in the filename.

You can get more information about multidimensional acquisition in the Knowledge Base on the ONI website.