Can we do amplification of our target along with constitutive gene in the same tube(both sets of primers in same tube) when their lengths are resolvable ? If yes why it is not practicable(/this avoids technical error and more labour)? if no, why not(/constitutive gene competes with target for PCR components)? I am  Curious to know the reason behind the regular practicing of RT-PCR.

Thank you.

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