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• 23:42, 21 October 2021 Biakiti (Talk | contribs) uploaded File:T--USP-Brazil--IGEM-USP-Description-Fusionedcyp2.png
• 23:25, 21 October 2021 Biakiti (Talk | contribs) uploaded File:T--USP-Brazil--IGEM-USP-Description-Fusionedcyp1.png (Schematic representation of the P450-redox partner interaction. P450, cytochrome 450 monooxygenase; CPR, cytochrome P450 reductase; FAD, flavin adenine dinucleotide; FMN, flavin mononucleotide; NADPH, reduced nicotinamide adenine dinucleotide phosphate.)
• 19:25, 21 October 2021 Biakiti (Talk | contribs) uploaded File:T--USP-Brazil--IGEM-USP-Description-CYP6g1Model.png
• 19:24, 21 October 2021 Biakiti (Talk | contribs) uploaded File:File-File-T--USP-Brazil--IGEM-USP-Description-GUSpollen.png (Figure 1. Presence of GUS activity on plants. (-C) - Pollen negative control. (+C) - Leaf positive control (GUS expressed by CaMV35S promoter). 2 and 22 - Transformants Micro-tom for our circuit. Blue pollen cells are indicated by arrows in pictures 2...)
• 19:24, 21 October 2021 Biakiti (Talk | contribs) uploaded File:File-T--USP-Brazil--IGEM-USP-Description-qRTPCRtable.png
• 19:18, 21 October 2021 Biakiti (Talk | contribs) uploaded File:T--USP-Brazil--IGEM-USP-Description-Lat52GUS.png (Figure 2. Schematic representation for β-glucuronidase (GUS) assay on pollen. The catalysis of X-Gluc produces a chromophore that can be easy to visualize and shows the traduction of transcript.)
• 18:36, 21 October 2021 Biakiti (Talk | contribs) uploaded File:T--USP-Brazil--IGEM-USP-Description-Lat52 Overall.png (Figure 1.Scheme of steps for RT-qPCR. RNA from leaf and pollen are extracted and purified, then the samples are used as template for cDNA synthesis. Next, the standardized cDNA was used to perform the qRT-PCR to prove the difference of transcripts rate.)