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. Author manuscript; available in PMC: 2011 Jan 1.
Published in final edited form as: J Cell Physiol. 2010 Jan;222(1):200–208. doi: 10.1002/jcp.21938

Fig. 3. Assessment of microarray data reliability.

Fig. 3

(A) 5 µg of total RNA from T98G glioblastoma cells treated as indicated were analyzed via northern blot to verify changes in expression for a selected group of genes (left panels). Microarray data are visualized as heat maps showing changes in expression (log2 ratios) obtained from the microarray hybridizations according to the color scale included below. (B) T98G cells were transduced with Ad-tTA and Ad-T-dnCDK9 for 6 h. Identical sets of transduced cells were incubated with tetracycline or vehicle for 42 additional h. Cells were harvested for western and northern blot analyses as described in Fig. 1 and Fig. 2A, respectively. Northern blot analysis and corresponding microarray data are shown as in A (C) Bar graph representing the average expression change (log2 ratio) in expression for transcripts modulated by CDK9 inhibition, which are detected by more than one probe set in the microarray. Standard deviation error bars are shown.