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Unusual stability of messenger RNA in snake venom reveals gene expression dynamics of venom replenishment.

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Figure

Figure 1. PCR amplification of cDNA constructed from venom
Figure 2. Venom mRNA expression profiles during venom re-synthesis. Relative expression profiles of six venom transcripts (snake venommetalloproteinase, serine protease, C-type lectin, Kunitz inhibitors, protein disulphide isomerase and QKW inhibitory pept
Table 1. Statistical analysis of relative gene expression byquantitative PCR.
Figure 3. HPLC and mass spectrometry analysis of pooled venom samples from Ghana and Nigeria during venom re-synthesis.HPLC-MS/MS identification of proteins from pooled Ghanaian and Nigerian venom samples showed that very little quantitative changes in the
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