Template:Team:USyd-Australia/Calendar/Events List

From 2014.igem.org

(Difference between revisions)

@@ Line 32: / Line 32: @@
 { title: 'Plasmid prep of psB6A1, Checking: finish digests, gel electrophoresis of digests',
 	start: new Date(2014,9,7),
-	description: 'Details: Gel electrophoresis (100V, 400mA, 30min)<br><br>Result: Gel broke. pSB6A1 yielded 5104.1ng/uL DNA & (A260/280) 1.62.<br><br>Conclusion: Possible protein contamination to samples<br><br>-  Abi'},
+	description: 'Details: Gel electrophoresis (100V, 400mA, 30min)<br><br>Result: Gel broke. pSB6A1 yielded 5104.1ng/uL DNA &amp; (A260/280) 1.62.<br><br>Conclusion: Possible protein contamination to samples<br><br>-  Abi'},
 { title: 'Plasmid prep of pSB6A1, Re-doing digest',
 	start: new Date(2014,10,7),
@@ Line 41: / Line 41: @@
 { title: 'Plasmid prep of pUS44, Re-doing digest',
 	start: new Date(2014,16,7),
-	description: 'Details: Restriction digest. Did the protocol change?<br><br>Conclusion: Nanospec: 395.5ng/mL DNA yield<br><br>-  Abi & Tom'},
+	description: 'Details: Restriction digest. Did the protocol change?<br><br>Conclusion: Nanospec: 395.5ng/mL DNA yield<br><br>-  Abi &amp; Tom'},
 { title: 'Construction of pUS201, PCR of pSB6A1 using iGEM401/402 primers ',
 	start: new Date(2014,24,7),
@@ Line 62: / Line 62: @@
 { title: 'construction of pUS201, re-doing pSB1C3 PCR with iGEM1403/1404',
 	start: new Date(2014,3,8),
-	description: 'Details: PCR Master mix with 1403/1404 primers. Used iGEM psB1C3. Ran on regular program PCR ~2HRS<br><br>Result: Products stored in the fridge<br><br>-  Jeanne & Callum'},
+	description: 'Details: PCR Master mix with 1403/1404 primers. Used iGEM psB1C3. Ran on regular program PCR ~2HRS<br><br>Result: Products stored in the fridge<br><br>-  Jeanne &amp; Callum'},
 { title: 'construction of pus201, Gel purification: gel electrophoresis of pSB1C3 PCR ',
 	start: new Date(2014,4,8),
-	description: 'Details: Gel purification electrophoresis (60V, 400mA, 1hr). Stained in gel red??? for 30min<br><br>Result: missing gel??<br><br>-  Jeanne & Callum'},
+	description: 'Details: Gel purification electrophoresis (60V, 400mA, 1hr). Stained in gel red??? for 30min<br><br>Result: missing gel??<br><br>-  Jeanne &amp; Callum'},
 { title: 'Checking pUS201 construct, Plasmid mini-Prep: to confirm pUS201 in top10 colonies',
 	start: new Date(2014,4,8),
-	description: 'Details: Incubated overnight to finish later<br><br>Result: Yield 5.7ng/ul, 1.61 260/280<br><br>Conclusion: Yield too low to use<br><br>-  Jeanne & Callum'},
+	description: 'Details: Incubated overnight to finish later<br><br>Result: Yield 5.7ng/ul, 1.61 260/280<br><br>Conclusion: Yield too low to use<br><br>-  Jeanne &amp; Callum'},
 { title: 'Checking IntI1 from SamR's construct, Restriction digest: SamR's pSB1C3+ARApBAD',
 	start: new Date(2014,7,8),
@@ Line 93: / Line 93: @@
 	start: new Date(2014,0,9),
 	description: 'Details: Transformation and then incubated overnight at 37 C<br><br>-  Abi and Tom'},
+{ title: 'Checking pUS201 construct, Re-checking the pUS201 by restriction digestion',
+	start: new Date(2014,3,9),
+	description: 'Details: Restriction digestion (EcoR1, NdeI, NdeI/BamHI, NdeI/HindIII)<br><br>'},
+{ title: 'construction of PUS204, Junction PCR to check whether pUS204 has been ligated successfully',
+	start: new Date(2014,8,9),
+	description: 'Details: Junction PCR with iGEM1407/iGEM1408 primers and Taq<br><br>Result: Products plated for…why?<br><br>-  Tom'},
+{ title: 'Construction of pUS203, Checking: heat-killing and running a gel of products',
+	start: new Date(2014,9,9),
+	description: 'Details: Heat killed construct at 80 C for 20 min. Ran a gel electrophoresis of products wfor 100V for 1hr.<br><br>Result: Gel failed.<br><br>Conclusion: Gibson Assembly attempted anyway, gel fail was not indication of no construct<br><br>-  Tom'},
+{ title: 'Construction of pUS201, Plating out Pus201 Gibson Assembly',
+	start: new Date(2014,9,9),
+	description: 'Details: Plated out GA products onto Amp plates.<br><br>-  Tom'},
+{ title: 'Construction of pUS204, Junction PCR gel',
+	start: new Date(2014,9,9),
+	description: 'Details: Gel electrophoresis with PCR products (overnight pSB1C3/aeBlue cultures, 1hr growth cultures, no plasmid colony, no template control)<br><br>Result: ??<br><br>Conclusion: ??<br><br>'},
+{ title: 'Checkin pUS203, Patch plate Int1I-2 and SamR construct',
+	start: new Date(2014,10,9),
+	description: 'Details: GA product cultures transferred to patch plates using 25x "small" colonies and 25x"large" colonies.<br><br>Result: Colonies to be screened with junction PCR. Why patch plate?<br><br>Conclusion: ?<br><br>-  ?'},
+{ title: 'Checking Pus203, Preperation of colony PCR of PUS203: of the "small" and "large" colonies on patch plate',
+	start: new Date(2014,11,9),
+	description: 'Details: PCR with Hs463a and Hs464 primers and Taq.<br><br>'},
+{ title: 'Checking Pus203, colony PCR of PUS203: of the "small" and "large" colonies on patch plate',
+	start: new Date(2014,14,9),
+	description: 'Details: PCR with Hs463a and Hs464 primers and Taq.<br><br>Result: Expected fragment size was 473bp. No data received. ????<br><br>Conclusion: ?? Re-do?<br><br>-  rokiah'},
 			]
 		});

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Revision as of 04:36, 14 October 2014