Real lab failures, root causes, and fixes — curated and bilingually annotated by our team.
Bioanalyzer or gel electrophoresis reveals smearing or loss of distinct RNA bands. RNA integrity number (RIN) is significantly reduced compared to input material.
Purified RNA fails to perform as expected in RT-PCR, RT-qPCR, RNA-seq library preparation, or other downstream assays despite acceptable concentration and A260/280 ratio.
Spectrophotometric analysis shows A260/230 ratio below 1.8-2.0, indicating residual guanidine salt or other chaotropic agent contamination in the purified RNA.
Recovered RNA concentration is significantly lower than expected based on input amount. Spectrophotometric measurement shows inadequate RNA quantity for downstream applications.
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