From 2007.igem.org

Revision as of 12:10, 25 October 2007 (view source) Sunlovedie (Talk | contribs) ← Older edit		Revision as of 07:48, 26 October 2007 (view source) Lovecarrot (Talk | contribs) Newer edit →
Line 7:		Line 7:
	Figure 2: This figure shows the concentration variation of chemical moleculars when the input signal is at negative edge when t=0.		Figure 2: This figure shows the concentration variation of chemical moleculars when the input signal is at negative edge when t=0.
	[[Image:tjumodel11b.jpg|500px]]<br>		[[Image:tjumodel11b.jpg|500px]]<br>
		+
		+	Figure 3: This graph shows the variation of AHL,cI,LuxR and GFP responding to the addition of input
		+	signal(IPTG). It is easy to find that the level of AHL and cI shares the same changing tendency
		+	with that of IPTG, whereas the contents of LuxR protein changes inversely with that of IPTG.
		+	Therefore, the output signal (GFP) only exists at the edge of IPTG curves where the input signal
		+	switches from 1 to 0 or from 0 to 1.
	[[Image:TJUMODELFF203.jpg|800px]]<br>		[[Image:TJUMODELFF203.jpg|800px]]<br>
	|}		|}

---

Revision as of 07:48, 26 October 2007

These two pictures are drew with the same parameters coming from related literature.Both figers point out that the output signal(GFP,yellow line) will form a pulse immediately after the input signal alters.
Figure 1: This figure shows the concentration variation of chemical moleculars when the input signal is at positive edge when t=0.

Figure 2: This figure shows the concentration variation of chemical moleculars when the input signal is at negative edge when t=0.
Figure 3: This graph shows the variation of AHL,cI,LuxR and GFP responding to the addition of input signal(IPTG). It is easy to find that the level of AHL and cI shares the same changing tendency with that of IPTG, whereas the contents of LuxR protein changes inversely with that of IPTG. Therefore, the output signal (GFP) only exists at the edge of IPTG curves where the input signal switches from 1 to 0 or from 0 to 1.