Team:Chiba/Calendar-Home/26 August 2008

From 2008.igem.org

(Difference between revisions)
(Team:Communication)
(Team:Output)
Line 216: Line 216:
[[Team:Chiba/protocol/digestion|Digestion]]
[[Team:Chiba/protocol/digestion|Digestion]]
-
*vector:[http://partsregistry.org/Part:BBa_F2620 BBa_F2620]
+
*vector:[http://partsregistry.org/Part:BBa_F2620 BBa_F2620](1)
<table width="250" border="4" cellpadding="0" cellspacing="0" bordercolor="#000000">
<table width="250" border="4" cellpadding="0" cellspacing="0" bordercolor="#000000">
<tr>
<tr>
<td width="257">Sample No.</td>
<td width="257">Sample No.</td>
-
<td></td>
+
<td>1</td>
</tr>
</tr>
<tr>
<tr>
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</tr>
</tr>
<tr>
<tr>
-
<td>SpeⅠ</td>
+
<td>SpeI</td>
<td>2</td>
<td>2</td>
</tr>
</tr>
<tr>
<tr>
-
<td>PstⅠ</td>
+
<td>PstI</td>
<td>2</td>
<td>2</td>
</tr>
</tr>
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</table>
</table>
-
*insert:[http://partsregistry.org/Part:BBa_J52008 BBa_J52008]
+
*insert:[http://partsregistry.org/Part:BBa_J52008 BBa_J52008](1)
-
:[http://partsregistry.org/Part:BBa_E2030 BBa_E2030]
+
:[http://partsregistry.org/Part:BBa_E2030 BBa_E2030](2)
<table width="250" border="4" cellpadding="0" cellspacing="0" bordercolor="#000000">
<table width="250" border="4" cellpadding="0" cellspacing="0" bordercolor="#000000">
<tr>
<tr>
<td width="257">Sample No.</td>
<td width="257">Sample No.</td>
-
<td></td><td></td>
+
<td>1</td><td>2</td>
</tr>
</tr>
<tr>
<tr>
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</tr>
</tr>
<tr>
<tr>
-
<td>XbaⅠ</td>
+
<td>XbaI</td>
<td>1</td><td>1</td>
<td>1</td><td>1</td>
</tr>
</tr>
<tr>
<tr>
-
<td>PstⅠ</td>
+
<td>PstI</td>
<td>1</td><td>1</td>
<td>1</td><td>1</td>
</tr>
</tr>
<tr>
<tr>
-
<td>DpnⅠ</td>
+
<td>DpnI</td>
<td>1</td><td>1</td>
<td>1</td><td>1</td>
</tr>
</tr>
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[[Team:Chiba/protocol/ligation/ligation|Ligation]]
[[Team:Chiba/protocol/ligation/ligation|Ligation]]
-
*vector:[http://partsregistry.org/Part:BBa_F2620 BBa_F2620] insert:[http://partsregistry.org/Part:BBa_J52008 BBa_J52008]
+
*vector:[http://partsregistry.org/Part:BBa_F2620 BBa_F2620] insert:[http://partsregistry.org/Part:BBa_J52008 BBa_J52008](1)
-
*vector:[http://partsregistry.org/Part:BBa_F2620 BBa_F2620] insert:[http://partsregistry.org/Part:BBa_E2030 BBa_E2030]
+
*vector:[http://partsregistry.org/Part:BBa_F2620 BBa_F2620] insert:[http://partsregistry.org/Part:BBa_E2030 BBa_E2030](2)
-
*Negative control:[http://partsregistry.org/Part:BBa_F2620 BBa_F2620]
+
*Negative control:[http://partsregistry.org/Part:BBa_F2620 BBa_F2620](3)
<table width="250" border="4" cellpadding="0" cellspacing="0" bordercolor="#000000">
<table width="250" border="4" cellpadding="0" cellspacing="0" bordercolor="#000000">
<tr>
<tr>
<td width="257">Sample No.</td>
<td width="257">Sample No.</td>
-
<td></td><td></td><td></td>
+
<td>1</td><td>2</td><td>3</td>
</tr>
</tr>
<tr>
<tr>

Revision as of 20:11, 29 October 2008

>Home | Notebook

25 August 2008 <|> 27 August 2008

Contents

Laboratory work

Team:Input

no work

Team:Communication

(8/25)--->Gel Check
Chiba-0825-2.JPG
Sample No. 1~3
Sample DNA(μL) 30
Loading Dye(μL) 6
TOTAL(μL) 36


1, BBa_C0178
Insert:609bp -> OK
Chiba-0825-3.JPG
2, BBa_C0170
Insert:609bp -> OK
Chiba-0825-4.JPG
3, BBa_J04500(2007)
--> OK


--->Gel Extract


--->Zymo Clean
eluted with following amount of elution buffer
  1. 5μl
  2. 5μl
  3. 27μl


--->Gel Check
Chiba-0825-5.JPG
Sample No. 1~3
Sample DNA(μL) 2
Loading Dye(μL) 2
H2O(μL) 8
TOTAL(μL) 12
From left;
  1. insert:BBa_C0178 --> OK
  2. insert:BBa_C0170 --> OK?
  3. vector:BBa_J04500 --> OK


--->SAP
Sample No. 3
Sample DNA(μL) 26
SAP(μL) 1
SAP Buffer(μL) 3
TOTAL(μL) 30


--->Zymo Clean
Sample No.3 -->9μl


--->Gel Check
Chiba-0826.JPG
Sample No.3 1
Loading Dye(μL) 1
dH2O(μL) 4
TOTAL(μL) 6
Sample No.3 -> OK ・・・30ng?


--->Ligation
Sample No. (1)(2)(3)(4)(5)
insert(1)BBa_C0178(μL) 1--1-
insert(2)BBa_C0170(μL) -1--1
vector(3)BBa_J04500(μL) --222
ligase(μL) 11111
Buffer(μL) 22222
dH2O(μL) 66544
TOTAL(μL) 1010101010


--->Transformation
  1. insert(1)BBa_C0178
  2. insert(2)BBa_C0170
  3. vector(3)BBa_J04500
  4. insert(1)BBa_C0178+vector(3)BBa_J04500
  5. insert(2)BBa_C0170+vector(3)BBa_J04500

Team:Output

Gel Check

Sample No.
DNA tamplate 11111
Loading Dye 11111
dH2O 44444
TOTAL 6μl6μl6μl6μl6μl

Digestion

Sample No. 1
DNA tamplate 100
SpeI 2
PstI 2
BSA(x10) 13
Buffer2 13
TOTAL 130μl
BBa_E2030(2)
Sample No. 12
DNA tamplate 3030
XbaI 11
PstI 11
DpnI 11
Buffer3 44
BSA(x10) 44
TOTAL 40μl40μl


-->37°C 3hour
-->SAP
-->37°C 30min
-->65°C 15min
-->Zymo Clean

Ligation

Sample No. 123
vector 555
inser 107.50
Ligase Buffer 444
Ligase 111
dH2O 02.510
TOTAL 20μl20μl20μl

-->RT 2hour

-->Transformation(XL10G)

-->37°C over night

-->colony PCR

-->Mini prep