Team:NTU-Taida/Result
From 2012.igem.org
Line 1: | Line 1: | ||
{{:Team:NTU-Taida/Templates/Header}}{{:Team:NTU-Taida/Templates/Navbar}}{{:Team:NTU-Taida/Templates/Sidebar}}{{:Team:NTU-Taida/Templates/ContentStart}} | {{:Team:NTU-Taida/Templates/Header}}{{:Team:NTU-Taida/Templates/Navbar}}{{:Team:NTU-Taida/Templates/Sidebar}}{{:Team:NTU-Taida/Templates/ContentStart}} | ||
{{:Team:NTU-Taida/Templates/BSHero|Title=Result|Content=<p>Testing Hero</p>}} | {{:Team:NTU-Taida/Templates/BSHero|Title=Result|Content=<p>Testing Hero</p>}} | ||
- | + | == '''Results''' == | |
- | =='''Results'''== | + | |
===Secretion system=== | ===Secretion system=== |
Revision as of 07:38, 23 September 2012
Result
Testing Hero
Contents |
Results
Secretion system
In order to evaluate the secretion system, we combined our products and signal peptides (SP1,SP2 and SP3). We de novo synthesized the following peptide genes: signal peptide 1(SP1)-CPP-Flag; signal peptide 2(SP2)-CPP-Flag; signal peptide 3(SP3)-CPP-Flag; SP1-GLP-1. By linking these peptide genes with constitutively-expressed promoter and ribosome-binding site, we use either Escherichia coli K12 DH5α or Escherichia coli BL-21 strain to express them. Later, we used several methods to identify the target peptides in the extracellular fluid, the outer environment. Those methods include the dot-immunoblotting, ELISA and Western blotting. Those methods’ detail description are as below and the results are being discussed in detail.
Dot immunoblotting
Western blotting
ELISA