Yes, but you have to add the adjustment to your materials and method section. E.g microscope images were further adjusted I'm imageJ to increase the intensity signal. Although, the image I showed in this tutorial is bright under the microscope, when I opened it in imageJ, it looks darker. The only edit I normally apply would be to use the RESET on the contract/brightness window. Then I get a brighter image and I don't have to add that yo material and methods
![ปฏิเสธไม่ไหว (Crush on you) - LIPTA feat. No One Else [Official MV]](http://i.ytimg.com/vi/NBw1jF342vw/mqdefault.jpg)
Thank you! This is exactly what I needed for lab!!!!! life saver
You're very much welcome.
vielen Danke
Gerne!
Can i use these adjustments in imageJ for publications?
Yes, but you have to add the adjustment to your materials and method section. E.g microscope images were further adjusted I'm imageJ to increase the intensity signal.
Although, the image I showed in this tutorial is bright under the microscope, when I opened it in imageJ, it looks darker. The only edit I normally apply would be to use the RESET on the contract/brightness window. Then I get a brighter image and I don't have to add that yo material and methods
Could you post a video on how to properly threshold to separate a cluster of cells to individual cells
Hello, I will work on that and hopefully upload the video by the weekend.
Thank you so much!
You're welcome 😊