Hi,

I have labeled my sperm cell samples with FITC conjugated lectins and have captured files in Tiff formats. Now I want to measure fluorescent intensity by using IMAGE J software. According to the intensity measurement procedure, I'm following the same steps as mentioned in the IMAGE J manual. But I have one confusion before going to intensity measurement that what are the bases of the selection of 8 bit, 16 bit, 32 bit and RGB type to process tiff files for conversion into gray-scale? please suggest to me how and why I have to select the image type mentioned above???

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