Team:Stockholm/23 October 2010
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===IgG protease activity assay=== | ===IgG protease activity assay=== | ||
+ | Finished the repeated experiment and read the wavelength at 450 nm. | ||
+ | |||
+ | '''Blank:''' 80 μl PBS + 100 μl SureBlue™ peroxidase substrate + 100 μl 1 M HCl. | ||
+ | |||
+ | {|border="1" cellpadding="1" cellspacing="0" | ||
+ | !colspan="14"|Sample loading | ||
+ | |- | ||
+ | !width="50"|Ab dil. | ||
+ | |width="50"| | ||
+ | !width="50"|1 | ||
+ | !width="50"|2 | ||
+ | !width="50"|3 | ||
+ | !width="50"|4 | ||
+ | !width="50"|5 | ||
+ | !width="50"|6 | ||
+ | !width="50"|7 | ||
+ | !width="50"|8 | ||
+ | !width="50"|9 | ||
+ | !width="50"|10 | ||
+ | !width="50"|11 | ||
+ | !width="50"|12 | ||
+ | |- | ||
+ | !1:500 | ||
+ | !A | ||
+ | |colspan="2" align="center"|Ind. IgGp A | ||
+ | |colspan="2" align="center"|Ind. IgGp B | ||
+ | |colspan="2" align="center"|Ind. SOD A | ||
+ | |colspan="2" align="center"|Ind. SOD B | ||
+ | |colspan="2" align="center"|Unind. IgGp A | ||
+ | |colspan="2" align="center"|Unind. IgGp B | ||
+ | |- | ||
+ | !1:250 | ||
+ | !B | ||
+ | |colspan="2" align="center"|Ind. IgGp A | ||
+ | |colspan="2" align="center"|Ind. IgGp B | ||
+ | |colspan="2" align="center"|Ind. SOD A | ||
+ | |colspan="2" align="center"|Ind. SOD B | ||
+ | |colspan="2" align="center"|Unind. IgGp A | ||
+ | |colspan="2" align="center"|Unind. IgGp B | ||
+ | |- | ||
+ | !– | ||
+ | !C | ||
+ | |align="center"|PBS 1:500 | ||
+ | |align="center"|PBS 1:250 | ||
+ | |align="center"|Blank | ||
+ | |align="center"|– | ||
+ | |align="center"|– | ||
+ | |align="center"|– | ||
+ | |align="center"|– | ||
+ | |align="center"|– | ||
+ | |align="center"|– | ||
+ | |align="center"|– | ||
+ | |align="center"|– | ||
+ | |align="center"|– | ||
+ | |} | ||
+ | |||
+ | ====Results==== | ||
+ | {|border="1" cellpadding="1" cellspacing="0" | ||
+ | !colspan="13"|A<sub>450</sub> measurements | ||
+ | |- | ||
+ | |width="50"| | ||
+ | !width="50"|1 | ||
+ | !width="50"|2 | ||
+ | !width="50"|3 | ||
+ | !width="50"|4 | ||
+ | !width="50"|5 | ||
+ | !width="50"|6 | ||
+ | !width="50"|7 | ||
+ | !width="50"|8 | ||
+ | !width="50"|9 | ||
+ | !width="50"|10 | ||
+ | !width="50"|11 | ||
+ | !width="50"|12 | ||
+ | |- | ||
+ | !A | ||
+ | |align="center"|0.073 | ||
+ | |align="center"|0.075 | ||
+ | |align="center"|0.087 | ||
+ | |align="center"|0.087 | ||
+ | |align="center"|0.091 | ||
+ | |align="center"|0.094 | ||
+ | |align="center"|0.089 | ||
+ | |align="center"|0.090 | ||
+ | |align="center"|0.131 | ||
+ | |align="center"|0.132 | ||
+ | |align="center"|0.109 | ||
+ | |align="center"|0.108 | ||
+ | |- | ||
+ | !B | ||
+ | |align="center"|0.116 | ||
+ | |align="center"|0.126 | ||
+ | |align="center"|0.116 | ||
+ | |align="center"|0.117 | ||
+ | |align="center"|0.156 | ||
+ | |align="center"|0.158 | ||
+ | |align="center"|0.145 | ||
+ | |align="center"|0.150 | ||
+ | |align="center"|0.181 | ||
+ | |align="center"|0.187 | ||
+ | |align="center"|0.125 | ||
+ | |align="center"|0.124 | ||
+ | |- | ||
+ | !C | ||
+ | |align="center"|0.003 | ||
+ | |align="center"|0.011 | ||
+ | |align="center"|'''0.000''' | ||
+ | |align="center"|– | ||
+ | |align="center"|– | ||
+ | |align="center"|– | ||
+ | |align="center"|– | ||
+ | |align="center"|– | ||
+ | |align="center"|– | ||
+ | |align="center"|– | ||
+ | |align="center"|– | ||
+ | |align="center"|– | ||
+ | |} | ||
+ | |||
+ | Unfortunately no pattern seen for the different samples. It seems like something else but the protein extracts is affecting proteolysis of the secondary antibodies. Maybe the primary antibodies conjugated to the agarose is not evenly distributed. Either way, it seems like the digestion is the result of proteolysis by ''E. coli'' proteases, not overexpressed IdeS. | ||
+ | |||
+ | {{Stockholm/Footer}} |
Latest revision as of 11:13, 26 October 2010
Andreas
IgG protease activity assay
Finished the repeated experiment and read the wavelength at 450 nm.
Blank: 80 μl PBS + 100 μl SureBlue™ peroxidase substrate + 100 μl 1 M HCl.
Sample loading | |||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Ab dil. | 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 10 | 11 | 12 | |
1:500 | A | Ind. IgGp A | Ind. IgGp B | Ind. SOD A | Ind. SOD B | Unind. IgGp A | Unind. IgGp B | ||||||
1:250 | B | Ind. IgGp A | Ind. IgGp B | Ind. SOD A | Ind. SOD B | Unind. IgGp A | Unind. IgGp B | ||||||
– | C | PBS 1:500 | PBS 1:250 | Blank | – | – | – | – | – | – | – | – | – |
Results
A450 measurements | ||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 10 | 11 | 12 | |
A | 0.073 | 0.075 | 0.087 | 0.087 | 0.091 | 0.094 | 0.089 | 0.090 | 0.131 | 0.132 | 0.109 | 0.108 |
B | 0.116 | 0.126 | 0.116 | 0.117 | 0.156 | 0.158 | 0.145 | 0.150 | 0.181 | 0.187 | 0.125 | 0.124 |
C | 0.003 | 0.011 | 0.000 | – | – | – | – | – | – | – | – | – |
Unfortunately no pattern seen for the different samples. It seems like something else but the protein extracts is affecting proteolysis of the secondary antibodies. Maybe the primary antibodies conjugated to the agarose is not evenly distributed. Either way, it seems like the digestion is the result of proteolysis by E. coli proteases, not overexpressed IdeS.