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. 2009 Mar 19;4(3):e4936. doi: 10.1371/journal.pone.0004936

Figure 4. Quantitative RT-PCR confirms upregulation of GLUT1 and GluR2.

Figure 4

Total RNA (2 µg) was used to generate cDNA by reverse transcription using oligo-dT primers. Note increased mRNA levels of glutamate transporter (GLUT1) and GluR2 in IAD patients compared to controls. Data are mean values ±SEM comparing 4 control and 4 IAD patients. βCAMKII and GAP43 do not show significant change in mRNA levels. GAP-3 (p<0.1), GLUT1 (* p<0.01), GluR2 (# p<0.03), βCAMKII (p<0.06).