I want to treat the HepG2 cells with either T3 or GC1 (TR-beta1 agonist) for 24 hours. I'm not sure about the internal control for qRT-PCR, in order to accurate normalisation of gene expression.
Please give me guidance.
I used qRT-PCR, in plant viruses gene expression. It is useful as a quantitative method. Best regards.
You can use several useful controls, such as 16S RNA, GAPDH, beta-Actin etc.
Dear Andreas,
Thanks for your guidance
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