Category:Team Lappish Hag's Love Potion

table 3 shows the specific activity of the ACS protein in various strains when grown on various carbon souces. Strain MS1 showed not ACS activity when grown on any carbon sources. When complemented with a plasmid carrying the acsA gene, ASC activity was detected in MS1

Figure 1 shows cell proliferation in pten mutants to be within a statistically significant time as the positive control. Figure 2 shows the similarity in pten mutants compared to oncogenic cultures known for cell proliferation.

Figure 1: BglA activity was detected when cellulose was provided as the sole carbon source. No activity detected when grown on other carbon sources.

Figure 4: ChrC was purified by affinity chromatography. The results of activity stain indicate ChrC is a SOD.

figure 6: dcrA mutants show a decrease in viable cells when exposed to oxygen

figure 7: results of oxygen capillary experiment show that dcrA mutants do not migrate from oxygen source compared to wildtype cells.

figure 3 show growth rates of alkB1 mutants on different n-alkanes. the growth rate was lowered in alkB1 mutants grown on n-hexane, while not affected when grown on other alkanes. This shows that alkB1 is involved in the degradation of n-hexane, while other enzymes are involved in the degradation of longer chain alkanes.

Figure 5 show the growth rate of both wild type and ppcA mutants when grown with acetate as an electron donor and both fumarate and iron(III) as electron acceptors. The growth rate of the mutant was decreased when Fe(III) was used as an electron acceptor. Combined with Table 3 which illustrates the reduction rates of several compounds in wild type an mutant suggests that ppcA is a carrier of electrons from acetate to iron(III) reductases.

Figure 2 demonstrates sociosexual interactions are olfactory mediated based on the activity data of MF, MM, and FF couples. Figure 3 reveals the decrease in SSI of Or47b-ablated flies. The SSI activity of males is shown to be dependent on olfactory senses according to Figure 4.

Figure 3 shows results of run off transcription assay. No transcription without cnrH. In the presence of cnrH transcription from cnrC and cnrY is activated.

Figure 1 shows complementation assay. E. coli with deleted zitB showed high zinc accumulation whereas E. coli with the deletion that were complemented with czcD from R. metallidurans showed lower levels of zinc accumulation.

Table 3 demonstrates homology with known metalloproteases from other bacteria.

Figure 4 confirms proteolytic activity of prtA in Erwinia by demonstrating inhibition by several common protease inhibitors.

Figure 2 demonstrates the allelic expression of Lamin A and Lamin C genes and Figure 1 provides the primer sequences used in the TaqMan assays for quantification of LMNA A and C transcripts.

Figure 8, complementation of E. coli acyl-CoA synthetase mutation by plasmid carrying alkK.