Hello. I cannot get this protocol to work, I was wondering if...
Hello. I cannot get this protocol to work, I was wondering if you have a reference troubleshooting guide? I use the same primary and secondary antibodies, purified and serial diluted mRNA, and same buffers, the only difference being I use BSA instead of non-fat milk.
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Hao Yu Author Answered May 9, 2021
Temasek Life Sciences Laboratory and Department of Biological Sciences, National University of Singapore, Singapore
There are many factors determining whether you can get good signals of dot blot, such as mRNA qualities, m6A abundance in the samples, crosslinking efficiency, etc. We suggest you to include some positive controls and try again.
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