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The presence of residual gold nanoparticles in samples interferes with the RT-qPCR assay used for gene expression profiling.

Natasha M SanabriaMary Gulumian
Published in: Journal of nanobiotechnology (2017)
AuNPs have the potential to interfere with the assay mechanism of RT-qPCR, thus, assay verification is required for AuNP-related gene expression studies used to evaluate toxicity. It is recommended to use HSP90 and YWHAZ as reference genes, i.e. these were the most stable in our study, irrespective of the source of the RNA, or, the point at which the AuNPs interacted with the assay. This report describes steps that can be utilised to generate a suitable method for gene expression studies associated with toxicity testing of various ENMs. For example, RNA standards that have been spiked with known amounts of ENMs should be run in conjunction with the unknown samples, in order to verify any RT-qPCR assay and determine the degree of error.
Keyphrases
  • gene expression
  • high throughput
  • gold nanoparticles
  • genome wide
  • dna methylation
  • oxidative stress
  • genome wide identification
  • single cell
  • climate change
  • heat shock protein
  • risk assessment
  • case control