Due to popular demand, I'll sporadically write up a series of posts on some ImageJ basics. For those not in the loop, ImageJ is a popular open source image processing program for microscopy; due to the availability of some rather sophisticated plugins, it can be a very powerful tool in the right hands. Also, the customiseable shortcuts are a blessing (and a curse for one's muscoloskeletal system, especially in the wrist region). I'm by no means anywhere near an expert with ImageJ (and don't do anything sophisticated, like macros or even much 3D/4D work), but there's a few basic things that I had to learn, and would like to share with anyone interested.
I put the rest of the post under the fold as most of you probably don't care...
I've been asked a few times to show how to calibrate the scale if it's not included in the image metadata. Probably about time I make some sort of reference post...
So what you need first is some sort of micrometer slide (microscope slide with a scale on it). Usually they come as a mm long thing that's divided 10x into 100um units, which are in turn subdivided again into 10um ones. So go ahead and dig one out of some dusty drawer in the corner of the microscopy room. If your lab is really disorganised/poor/prone to breaking stuff, a local core imaging facility should have one somewhere. I hear they usually accept bribes, such as chocolate. Be nice to them. Here a micrometer slide at 4x:
shouldn't cause a problem, but I've been told horror stories. And of course you have to take pictures of the scale bar specifically for each objective, even if you have two of the same mag. When imaging stuff later, be sure to keep track of specifically which objective was used. And, of course, try to get the best image you can.
So now you've got your calibration images. And let's assume you've got ImageJ up and running already. Let's walk through an example for our 40x air objective. Select the line tool, and carefully measure from start of one major line to the start of the next, or end to end. If you have 2 major (100um) divisions in one field of view, to help reduce error you can measure the 200um distance instead. Record the length in pixels; in this example, 2364/200um.
Now we know that under given conditions, the 40x scale is 2364pixels/200um, or 11.82pixels/um. Feel free to drop the 0.02, as our accuracy is nowhere near the hundreths of a pixel. In fact, the true scale is probably anywhere from 11.7-11.9, but, being biologists, we usually don't care about such precision anyway. Record this somewhere reliable, and preferrably accessible to your labmates (as much fun as it could be to watch them go through the ordeal all on their own, you'd probably want to present yourself as the nice guy/gal; that way, you'd be able to ask them 'kindly' to do things for you later on). Get the measurements for each of the objectives.
Now go to Analyze>Set Scale...
Which should bring up a menu. Enter the conversion ratio and specify units. If you're too lazy to divide your pixel/micron result, you can actually enter them here directly:
Check 'Global' if you want this scale to apply to all images in the current ImageJ session. Note, if IJ crashes or you restart the program for any other reason, you have to re-enter the scale each time. Should take a total of 2 seconds if you have all your ratios written down somewhere convenient (or memorised) though.
Click 'OK', and watch the magic happen: (also, test things out to make sure it shows ~100um between the 100um divisions)
To make a measurement, just hit ctrl+m or simply m on your keyboard. Go to Analyze>Set Measurements... to pick out which measurements you'd like to be recorded.
Making a scalebar
Now that we have the image scale all set up, we often need to include a scalebar somewhere in the image. IJ makes this process incredibly simple. S'pose for some rather surreal reason, we'd like a scalebar on our micrometer image. Select image window. Go to Analyze>Tools>Scale Bar
Now you can specify the width, height (thickness of the scalebar), font size, colour, whether you'd like there to be a box of a certain background colour behind the bar, where you'd like it in the image, and various text options (including whether you even want text in the first place)
OK that, and now you've got a scalebar. I've added mine to the keyboard shortcuts, so all I need to do to get one is hit 'b', check the width and location, and 'enter', and...done! Very convenient, especially once you've memorised the pixel/um ratios for your most frequently used objectives.
Was this post helpful at all? It's my first time making a tutorial like this, so please do let me know if anything is unclear/if I've failed miserably somewhere. Also, if anyone has any issues with ImageJ they'd like cleared up, feel free to share in the comments, and I *might* be able to say something useful. No guarantees though ^_^
Does expression of the toxA operon depend on ToxT as well as ToxA?
1 day ago in RRResearch