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. 2010 May 10;9:103. doi: 10.1186/1476-4598-9-103

Table 1.

Real-time quantitative RT-PCR for validation of microarray data

Gene Microarray data ΔCt (Ct LP-1D1b-Ct LP-1cl1) Fold change FC (microarray)
36B4 nm* -0.78/-0.52/-0.42** 1 -
CSN2 +7.33 -2.16/-2.70 +7.67/+6.34 +7.33
FGFR3 +5.07 -2.78/-1.62 +11.79/+4.25 +5.09
FHIT +4.67 -1.41/-1.10 +3.68/+3.68 +4.67
HSP90B1 +2.25 -1.21 +3.20 +2.26
TUBB2B -2.32 1.01 -1.45 -2.32
TFRC -6.48 3.77/3.14 -9.51/-6.36 -6.48
CD48 -12.27 4.05/4.18 -9.64/-13.08 -12.27

Gene Microarray data ΔCt (Ct LP-1K- Ct LP-1cl1) Fold change FC (microarray)

36B4 nm* -0.25/-0.40/-0.20/-0.36 1 -
LTB +40.66 -5.7 +43.71 +40.67
FN1 +13.54 -3.55 +8.87 +13.54
BCL2 +3.17 -2.36 +3.89 +3.17
CDK6 -4.14 1.83/1.95 -4.08/-4.43 -4.14
GAPDH -5.15 1.09 -2.44 -6.15
UCHL1 -63.82 11.11/11.25 -2538/-2797 -63.82

* nm, not modified. **When several numbers are indicated, they refer to the results obtained with different runs of PCR. For each sample, the average Ct value for the internal standard 36B4 was subtracted from the average Ct value for each gene to yield ΔCt. The relative amount of each mRNA compared to the calibrator (36B4) in each run was calculated by the formula N = 2-ΔΔCt to give the fold change. For each gene, the Fc calculated from microarray data (in bold) is reported in the right column.