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e , Relative abundance of SLC25A39, GCLM and SLC25A40 transcripts in HEK-293T cells treated with BSO (1 mM) for the indicated days using quantitative reverse transcription PCR (RT-qPCR), normalized to transcripts of -ACTIN

Analysis Coding region or mRNA sequences of the transgenes were retrieved from the NCBI nucleotide database and used as target sequences for analysis

tuberculosis (Cortes et al., Figure 4 MSMEG_2196 is a c-di-GMP synthetase encoding gene, the TSS of which was first determined in a previous study (Bharati et al., 5)

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