I am using Taqman to detect a transcript following a knockdown experiment of that gene in cells using esiRNA from Sigma (a mix of 19 siRNA sequences targeting different areas on the transcript of interest). Oddly, I am getting upregulation of this gene instead of downregulation. Anyone encountered this problem using Taqman? I should say that running the same samples using SYBR and standard primers resulted in the expected downregulation, but I am using Taqman to optimize the Real Time detection. Would appreciate any insight!