Team:Osaka/week1

From 2012.igem.org

(Difference between revisions)
 
(7 intermediate revisions not shown)
Line 1: Line 1:
-
{{Osaka}}
+
{{Osaka2}}
__NOTOC__
__NOTOC__
 +
==August 1 (Wed)==
==August 1 (Wed)==
# Preparation of LB agar plates (Amp)
# Preparation of LB agar plates (Amp)
# Restriction digests of parts (See Table 1)
# Restriction digests of parts (See Table 1)
 +
# Ligation
 +
#* 143(A): 124+1-1G(vector)
 +
#* 144(A): 125+1-1G(vector)
 +
#* 145(A): 126+1-1G(vector)
 +
#* 146(A): 127+1-1G(vector)
 +
#* 147(A): 128+1-1G(vector)
 +
#* 148(A): 129+1-1G(vector)
 +
#* 149(A): 138+1-1G(vector)
 +
#* 150(A): 139+1-1G(vector)
 +
#* 151(A): 140+1-1G(vector)
 +
#* 152(A): 141+1-1G(vector)
 +
# Transformation of ligation products into DH5α <i>E.coli</i>
 +
{|style="border-collapse: separate; border-spacing: 0; border-width: 1px; border-style: solid; border-color: #000; padding:5px;" cellpadding="5"
{|style="border-collapse: separate; border-spacing: 0; border-width: 1px; border-style: solid; border-color: #000; padding:5px;" cellpadding="5"
|+Table 1
|+Table 1
Line 28: Line 42:
|141||<bbpart>BBa_K602008</bbpart>||C|| <i>D. radiodurans</i> RecA expression device  
|141||<bbpart>BBa_K602008</bbpart>||C|| <i>D. radiodurans</i> RecA expression device  
|}
|}
-
 
-
 
-
# Ligation
 
-
#* 143(A): 124+1-1G(vector)
 
-
#* 144(A): 125+1-1G(vector)
 
-
#* 145(A): 126+1-1G(vector)
 
-
#* 146(A): 127+1-1G(vector)
 
-
#* 147(A): 128+1-1G(vector)
 
-
#* 148(A): 129+1-1G(vector)
 
-
#* 149(A): 138+1-1G(vector)
 
-
#* 150(A): 139+1-1G(vector)
 
-
#* 151(A): 140+1-1G(vector)
 
-
#* 152(A): 141+1-1G(vector)
 
-
# Transformation of ligation products
 
==August 2 (Thu)  ==
==August 2 (Thu)  ==
-
 
+
# Transfer to liquid culture:143~152
 +
#* Some parts didn't successfully transformed
==August 3 (Fri)  ==
==August 3 (Fri)  ==
 +
# Miniprep of yesterday's culture
 +
# Restriction digests of minipreppped parts
 +
# Gel electrophoresis of digests
 +
# Transformation of ligation products into DH5α <i>E.coli</i> again:147,148,150
-
 
+
==August 4 (Sat)  ==
-
==August 4 (Fri)  ==
+
# Transfer to liquid culture
-
 
+
# Restriction digests of 1-1G<vector> with SpeI,XbaI
 +
# Ligation
 +
# Transformation of ligation products into DH5α <i>E.coli</i>
 +
# Transformation of plasmid DNA into Rosetta <i>E.coli</i>:143~146,149,152
[[Team:Osaka/Notebook|Back to Notebook]]
[[Team:Osaka/Notebook|Back to Notebook]]

Latest revision as of 01:33, 14 September 2012


August 1 (Wed)

  1. Preparation of LB agar plates (Amp)
  2. Restriction digests of parts (See Table 1)
  3. Ligation
    • 143(A): 124+1-1G(vector)
    • 144(A): 125+1-1G(vector)
    • 145(A): 126+1-1G(vector)
    • 146(A): 127+1-1G(vector)
    • 147(A): 128+1-1G(vector)
    • 148(A): 129+1-1G(vector)
    • 149(A): 138+1-1G(vector)
    • 150(A): 139+1-1G(vector)
    • 151(A): 140+1-1G(vector)
    • 152(A): 141+1-1G(vector)
  4. Transformation of ligation products into DH5α E.coli
Table 1
numberPart NameResistanceDescription
124<bbpart>BBa_K602015</bbpart>C D. radiodurans PprI+PprA expression device
125<bbpart>BBa_K602016</bbpart>C D. radiodurans PprI+RecA expression device
126<bbpart>BBa_K602017</bbpart>C D. radiodurans PprA+RecA expression device
127<bbpart>BBa_K602018</bbpart>C D. radiodurans PprI+PprM expression device
128<bbpart>BBa_K602019</bbpart>C D. radiodurans PprA+PprM expression device
129<bbpart>BBa_K602020</bbpart>C D. radiodurans PprM+RecA expression device
138<bbpart>BBa_K602005</bbpart>C D. radiodurans PprI expression device
139<bbpart>BBa_K602006</bbpart>C D. radiodurans PprA expression device
140<bbpart>BBa_K602007</bbpart>C D. radiodurans PprM expression device
141<bbpart>BBa_K602008</bbpart>C D. radiodurans RecA expression device

August 2 (Thu)

  1. Transfer to liquid culture:143~152
    • Some parts didn't successfully transformed

August 3 (Fri)

  1. Miniprep of yesterday's culture
  2. Restriction digests of minipreppped parts
  3. Gel electrophoresis of digests
  4. Transformation of ligation products into DH5α E.coli again:147,148,150

August 4 (Sat)

  1. Transfer to liquid culture
  2. Restriction digests of 1-1G<vector> with SpeI,XbaI
  3. Ligation
  4. Transformation of ligation products into DH5α E.coli
  5. Transformation of plasmid DNA into Rosetta E.coli:143~146,149,152

Back to Notebook