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. 2006 Feb;80(4):1773–1786. doi: 10.1128/JVI.80.4.1773-1786.2006

TABLE 4.

Validation of microarray data by LightCycler kinetic RT-PCR

Gene product (designation) Samplea Fold increaseb
Microarray RT-PCR
Chemokine, C-X-C motif, ligand 10 (Cxcl10) PRV152, 96 h pi, Hyp 194.7 636.4
Complement component 3 (C3) PRV152, 96 h pi, Cer 2.9 2.1
Dual-specificity phosphatase 1 (Dusp1) PRV99G, 60 h pi, Cer 3.3 1.9
Guanylate nucleotide binding protein 2 (Gbp2) PRV152, 96 h pi, Cer 13.5 4.1
Interferon regulatory factor 7 (Irf7) PRV151, 60 h pi, Cer 2.1 1.7
Metallothionein 2 (Mt2) PRV151, 60 h pi, Hyp 14.8 6.8
Myxovirus resistance 1 (Mx1) PRV152, 96 h pi, Hyp 50.7 298.2
Neurogranin (Nrgn) PRV152, 60 h pi, Cer 9.4 13.5
Proteosome subunit, beta type 9 (Psmb9) PRV152, 96 h pi, Hyp 10.8 33.4
Serum/glucocorticoid-regulated kinase (Sgk) PRV151, 48 h pi, Hyp 5.4 3.7
Serum/glucocorticoid-regulated kinase (Sgk) PRV99G, 48 h pi, Cer 3.1 2.1
a

pi, postinfection; Hyp, hypothalamus; Cer, cerebellum.

b

Comparison of relative increases in mRNA accumulation of 10 selected gene products between respective PRV- and mock-infected samples (set to 1.0) as determined by microarray and RT-PCR analysis.