Figure 7.
Figure 7. Constitutive and CD40-enhanced transcription of cytoprotective genes. (A) Quantitative PCR of cDNAs from unstimulated BJAB cells with no transgene (▪), API2-MALT1 (□), or MALT1 (▨). Relative expression levels were normalized to glyceraldehyde-3-phosphate dehydrogenase (GAPDH) mRNA expression. Standard deviation bars were obtained from 2 independent experiments, each performed in triplicates. (B) In parallel, the same cells were stimulated with cross-linked CD40L for 4 hours and total RNA was extracted for quantitative RT-PCR analyses. (C) BJAB cells with and without the transgenes were stimulated with CD40 ligand for 0, 4, or 24 hours, and 30 μg of lysate was charged per lane and immunoblotted for BclXL and API2.

Constitutive and CD40-enhanced transcription of cytoprotective genes. (A) Quantitative PCR of cDNAs from unstimulated BJAB cells with no transgene (▪), API2-MALT1 (□), or MALT1 (▨). Relative expression levels were normalized to glyceraldehyde-3-phosphate dehydrogenase (GAPDH) mRNA expression. Standard deviation bars were obtained from 2 independent experiments, each performed in triplicates. (B) In parallel, the same cells were stimulated with cross-linked CD40L for 4 hours and total RNA was extracted for quantitative RT-PCR analyses. (C) BJAB cells with and without the transgenes were stimulated with CD40 ligand for 0, 4, or 24 hours, and 30 μg of lysate was charged per lane and immunoblotted for BclXL and API2.

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