Figure 4.
Figure 4. Quantitative PCR analyses. Total RNAs from erythroid tissues were amplified for detection of μ-globin (A) and α-globin (B). One million copies of DNA encoding α-globin (α clone) and μ-globin (μ clone) were included as negative controls to demonstrate specificity. Also shown is a comparison of μ-globin (C) and α-globin (D) expression levels in differentiating erythroblasts during culture (14 days) of CD34+ cells in erythropoietin (culture day on x-axis). All studies were performed in triplicate. Copy numbers were calculated by standard curve comparison. Mean values and standard deviation bars are shown. Asterisks indicate a significant change (t test; P < .001) compared with no significant (N.S.) change between fetal and adult erythroid tissues. For abbreviations, see the legend to Figure 3.

Quantitative PCR analyses. Total RNAs from erythroid tissues were amplified for detection of μ-globin (A) and α-globin (B). One million copies of DNA encoding α-globin (α clone) and μ-globin (μ clone) were included as negative controls to demonstrate specificity. Also shown is a comparison of μ-globin (C) and α-globin (D) expression levels in differentiating erythroblasts during culture (14 days) of CD34+ cells in erythropoietin (culture day on x-axis). All studies were performed in triplicate. Copy numbers were calculated by standard curve comparison. Mean values and standard deviation bars are shown. Asterisks indicate a significant change (t test; P < .001) compared with no significant (N.S.) change between fetal and adult erythroid tissues. For abbreviations, see the legend to Figure 3.

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