What is the best way to measure fluorescent comets whose tails are not oriented in the same direction?

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Why results of ROS flurescence are negative as there was no bacteria within?

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How to quantify the fluorescence intensity of only the merge area of an image using ImageJ software?

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How to determine LOD values?

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what all details we will get from fluorescence life time data

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Can someone please explain to me what power law statistics mean in single molecule fluorescence blinking ?

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Does anyone know how to improve calcium-imaging fluorescence with GRIN lenses?

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AL Timimi Zahra

Please read this article may be can help you

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2734468/

Regards

Asha Khanna

The article is not relevant.I am not talking about the length of poly A tails.Comet tails formed due to DNA damage are to be measured.We did it with comet score but it is efficient only for cells whose tails are in the same direction.