We want to analyse protein expression and metabolomics in mouse brains. The sampling method is snap-freezing in liquid nitrogen. Secondary outcome is blood analysis, which we plan to sample by cardiac puncture under terminal anesthesia.

Now we wonder whether the method of death can have any effects on the brain tissue data. Of course, blood withdrawal will cause hypoxia, which in turn will cause transcriptional changes etc.

But at what time frame is this to be expected?

Any advice is appreciated!

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