Team:TMU-Tokyo/Notebook/Assay 3 Protocol and Result

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2Centrifuged 10000 × g 5min<Br>
2Centrifuged 10000 × g 5min<Br>
3Remove the supernatant<Br>
3Remove the supernatant<Br>
-
4Wash the fungus<Br></p>
+
4Wash the fungus<Br>
 +
E. coli disrupted by sonicator in buffer of 50mM Tris-HCl pH7.2 .<Br>
 +
Centrifuged 10000 × g at 4 ℃  so that the enzyme is not deactivated, the supernatant was harvested as crude enzyme solution (If you want to save is stored at 4 ℃ in a cold room)
 +
 
 +
 
 +
</p>
<p class="description">
<p class="description">
<b>■Assay3 Result</b><Br>
<b>■Assay3 Result</b><Br>

Revision as of 16:27, 26 September 2012

 




■Experiment
1st week (8.13 - 8.19)
2nd week (8.20 - 8.26)
3rd week (8.27 - 9. 2)
4th week (9. 3 - 9. 9)
5th week (9.10 - 9.16)
6th week (9.17 - 9.23)
7th week (9.24 - 9.30)


■Protocols


■Assay
Device1 Assay
Device2 Assay
Device3 Assay




Assay 3



■Assay3 Protocol

1The cells were cultured at 30 ℃ for 18 hours in medium
2Centrifuged 10000 × g 5min
3Remove the supernatant
4Wash the fungus
E. coli disrupted by sonicator in buffer of 50mM Tris-HCl pH7.2 .
Centrifuged 10000 × g at 4 ℃ so that the enzyme is not deactivated, the supernatant was harvested as crude enzyme solution (If you want to save is stored at 4 ℃ in a cold room)

■Assay3 Result