nice video, I am assuming that you have to get the distance in pixels and known distance from your microscope that you used to take the pictures right?
@user-sk7cr5qx3w10 ай бұрын
This is really helpful video to know immunofluorescence quantification!
@najyajabeenpoolakkalody38627 ай бұрын
thank you so much.
@rabiazeb90517 ай бұрын
I added the scale bar to the image and now when I save it, it doesn't show the bar, I did several times but didn't, can anybody tell me what to do? I'm new on imageJ I don't know much about
@songohan393 Жыл бұрын
Veeery helpful thank you
@user-ql1nu5os5s Жыл бұрын
you saved my life friend
@wisamalton1625 ай бұрын
I have pics for MCF 7 cells in vitro stained by Phalloidin 488, how I can analyze them please? 😢
@tsmylovelybay4 ай бұрын
Thanks for your vdo
@gautamnisha7193 Жыл бұрын
Please complete the statistics.
@doughnut4692 жыл бұрын
Help me pls. How can I measure a timelap? Like 60 pictures in one file and i want to measure the process of changing intensity. I can only measure one at a time but cant let it measure 60 times each for a picture automatically
@user-yu1hb8pp5k5 ай бұрын
using macro in image J
@soumeyabenamar9790Ай бұрын
pleasse send for me the file, where can i find it!!???
Is this method correct tho? The programm calculates the mean intensity of the area you circle in. Imagine you make a big circle around your cell, the mean will be lower because most of the area is just black. If you now substract the mean intensity of the same circle in a empty area, your intensity will decrease even more And When you do a smaller circle just slightly bigger than the cell, the mean will be higher and if you substract the backround of this circle it will not substract that much because the backround is not even big. So the mean intensity will only be determined by how big you set the circle you want to measure and that is not comparable at all
@user-yu1hb8pp5k Жыл бұрын
you can use the threshold and then do analysis particle to choose the positive area only