Team:Tokyo-NoKoGen/protocols

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<title>'''Protocols'''</title>
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<p class="style3 f-lp"><strong><span class="style14"><a href="https://2011.igem.org/Team:Tokyo-NoKoGen/sponsors"><span class="style18" style="text-decoration:underline">Sponsors</span></a></span></strong></p>
<p class="style3 f-lp"><strong><span class="style14"><a href="https://2011.igem.org/Team:Tokyo-NoKoGen/sponsors"><span class="style18" style="text-decoration:underline">Sponsors</span></a></span></strong></p>
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<br><br>
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Protocols</font>
 +
 
 +
<h2>
 +
LB medium and LB agar gel
 +
Medium for cultivation of E. coli
 +
</h2>
 +
 
 +
<h3>LB medium (1 L)</h3>
 +
1; Add about 900 mL of distilled water to beaker.<br>
 +
2; Add 25 g of LB medium, Miller(MERCK) and stir. <br>
 +
3; Add distilled water up to 1 L and take LB medium to media bottle.<br>
 +
4; Autoclave for 20 min at 120°C.<br>
 +
 
 +
<h3>LB agar gel (1 L)</h3>
 +
1; Prepare LB medium without autoclave (Steps 1-3 of 1L scale of LB medium).<br>
 +
2; Add 15 g of agar and stirrer bar.<br>
 +
3; Autoclave for 20 minutes at 120°C.<br>
 +
4; Stir and cool LB medium with agar, add appropriate antibiotic (table).<br>
 +
5; Pour LB medium (Step 4) in plate and cool down in clean bench.<br>
 +
<br>
 +
 
 +
<table border="1">
 +
<td width="150"></td>
 +
<td align="right" width="150">f.c.</td><tr>
 +
<td width="150">Ampicillin</td>
 +
<td align="right" width="150">100 μg/mL</td><tr>
 +
<td width="150">Kanamycin</td>
 +
<td align="right" width="150">50 μg/mL</td><tr>
 +
<td width="150">Chloramphenicol </td>
 +
<td align="right" width="150">30 μg/mL</td><tr>
 +
<td width="150">Tetlacycline </td>
 +
<td align="right" width="150">11 μg/mL</td>
 +
</table><br><br>
 +
 
 +
<h2>Transformation</h2>
 +
<h3>Inserting plasmid into <i>E. coli</i></h3>
 +
1; Incubate frozen competent cell (DH5α) on the ice for a few minutes. <br>
 +
2; Add 1~5 μL of plasmid to competent cell (DH5α) on the ice.<br>
 +
3; Incubate for 20 – 30 minutes on the ice.<br>
 +
4; Incubate for 45 seconds at 42°C.<br>
 +
5; Add 1 mL LB medium and cultivate for 1 hour at 37°C.<br>
 +
6; Spread culture medium on LB agar plate with appropriate antibiotic.<br><br>
 +
 
 +
<h2>Plasmid extraction</h2>
 +
<h3>Preparation of plasmid extracted from <i>E. coli</i></h3>
 +
 +
1; Pick up single colony from agar plate and cultivate it in 1.5 mL LB medium containing appropriate antibiotic overnight at 37°C.<br>
 +
2; Move the culture medium to 1.5 mL tube.<br>
 +
3; Centrifuge for 5 seconds at 15,000×g and 4 °C and discard supernatant.<br>
 +
4; Add 100 μL Solution 1 to the pellet and resuspend and incubate for 3 minutes.<br>
 +
5; Add 100 μL Solution 2, invert tube gently 5 times and incubate for 3 minutes.<br>
 +
6; Add 100 μL Solution 3, invert tube 5 times and incubate for 3 minutes. <br>
 +
8; Add 200 μL Solution 4 and invert tube 5 times and centrifuge for 3 minutes at 15,000×g and 4 °C.<br>
 +
10; Take supernatant to new 1.5 mL tube and centrifuge for 3 minutes at 15,000×g and 4 °C.<br>
 +
11; Vortex Bind mix for 1 min and add 800 μL Bind mix to new 1.5 mL tube.<br>
 +
12; Add 400 μL supernatant after centrifugation (Step 10) to tube containing Bind mix (Step 11) and mix.<br>
 +
13; Incubate for 3 minutes, centrifuge for 3 seconds at 5,000×g and 4 °C, and discard supernatant.<br>
 +
14; Add 1 mL of 50% ethanol and resuspend. <br>
 +
15; Centrifuge for 3 seconds at 5,000×g and 4 °C and discard supernatant.<br>
 +
16; Repeat wash (Steps 14-15).<br>
 +
17; Dry pellet for a few minuet under a vacuum to remove residual ethanol.<br>
 +
18; Add 50 μL nuclease-free water or TE buffer and incubate for 3 minutes at 65°C.<br>
 +
19; Centrifuge for 3 minutes at 15,000×g and 4 °C.<br>
 +
19; 40 μL of supernatant into new 500 μL tube.<br><br>
 +
 
 +
<h2>Restriction enzyme digestion of DNA</h2>
 +
<h3>Cleavage of insert DNA from plasmid</h3>
 +
1; Mix DNA and restriction enzyme (Table).<br>
 +
2; Incubate for 2 hours at 37°C.<br>
 +
3; Incubate for 10 minutes at 65°C.<br>
 +
4; Confirm the band of DNA by agar gel electrophoresis.<br>
 +
<br>
 +
<br>
 +
<table border="1">
 +
<td width="150">reagent name</td>
 +
<td align="right" width="150">volume</td><tr>
 +
<td width="150">
 +
DNA<br>
 +
restriction enzyme A<br>
 +
restriction enzyme B<br>
 +
buffre
 +
MQ</td>
 +
<td align="right" width="150">
 +
5 μL<br>
 +
0.5 μL<br>
 +
0.5 μL<br>
 +
1.5 μL<br>
 +
7.5 μL
 +
</td><tr>
 +
<td width="150">total</td>
 +
<td align="right" width="150">15 μL</td>
 +
</table><br><br>
 +
 
 +
<h3>Confirmation and separation of digested DNA</h3>
 +
<h4>Preparation of agar gel</h4>
 +
1; Add 1 g of agar to 100 mL of 1×TAE.<br>
 +
2; Boil and stir until solution is dissolved and clear.<br>
 +
3; Cool down, pour into container to set its shape.<br>
 +
4; Wait until gel dries.<br>
 +
5; Store gel in 1×TAE.<br><br><br>
 +
 
 +
<h2>Agar gel electrophoresis</h2>
 +
1; Place agar gel and pour 1×TAE in electrophoresis chamber.<br>
 +
2; Load DNA ladder and DNA sample mixed with loading dye on agar gel.<br>
 +
3; Electrophorese for 20 minutes at 100 V.<br>
 +
4; Stain gel by Sybr SafeTM Gel Stain (Invitrogen).<br>
 +
5; Visualize the band of DNA using UV light.<br>
 +
6; Confirm the length of digested DNA.<br><br>
 +
 
 +
<h3>PCR</h3>
 +
1; Add 25 μL of reagent solution (Table 1) to PCR tube.<br>
 +
2; Amplify target DNA with PCR program (Table 2).<br>
 +
3; Confirm the band of DNA by agar gel electrophoresis.<br>
 +
<br>
 +
<table border="1">
 +
<td width="350">reagent name</td>
 +
<td align="right" width="100">volume</td><tr>
 +
<td width="350">
 +
primeSTAR® GXL DNA polymerase<br>
 +
5X GXL buffer<br>
 +
dNTP<br>
 +
template DNA<br>
 +
fowerd primer<br>
 +
reverse primer<br>
 +
MQ
 +
</td>
 +
<td align="right" width="100">
 +
0.5 μL<br>
 +
5 μL<br>
 +
2 μL<br>
 +
1 μL<br>
 +
1 μL<br>
 +
1 μL<br>
 +
14.5 μL
 +
</td><tr>
 +
<td width="350">total</td>
 +
<td align="right" width="100">25 μL</td>
 +
</table>
 +
Table 1
 +
<br>
 +
 
 +
<table border="1">
 +
<td width="60"></td>
 +
<td width="100">Step 1</td>
 +
<td width="200">Step 2</td>
 +
<td width="120">Step 3</td><tr>
 +
<td width="60">Cycle</td>
 +
<td width="100">1</td>
 +
<td width="200">30</td>
 +
<td width="120">1</td><tr>
 +
<td width="60"></td>
 +
<td width="100" height="150" align="middle" valign="top">98℃<br>
 +
1:00</td>
 +
<td width="200" valign="top">
 +
&nbsp;&nbsp;&nbsp;
 +
98℃<br>
 +
&nbsp;&nbsp;&nbsp;
 +
0:10<br>
 +
&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
 +
68℃<br>
 +
&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
 +
55℃
 +
&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
 +
4:00<br>
 +
&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
 +
0:10
 +
</td>
 +
<td width="120" valign="top"><br><br>
 +
&nbsp;&nbsp;&nbsp;68℃<br>
 +
&nbsp;&nbsp;&nbsp;2：00<br><br><br><br>
 +
&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;4℃<br>
 +
&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;∞</td>
 +
</table>
 +
Table2<br><br>
 +
 
 +
 
 +
 
 +
<h2>Gel purification</h2>
 +
<h3>Purification of DNA from agar gel</h3>
 +
<h4>GENECLEAN® II Kit(NaI、glass milk、NEW Wash)/Qbiogene</h4>
 +
1; Cut the objective band in the agar gel after electrophoresis and stain with SYBR Safe.<br>
 +
2; Put the gel including objective DNA into 1.5 mL tube and measure the mass of that.<br>
 +
3; Add 2.5-3 fold volume NaI solution into the tube (Gel: NaI =1 mg : 1 μL ).<br>
 +
4; Incubate the gel at 50°C for 5 minute.<br>
 +
5; Add 10 μL of glass milk and vortex.<br>
 +
6; Incubate for 5 minutes and vortex per a minute.<br>
 +
7; Centrifuge for 5 seconds at 15,000×g and 4°C and discard the supernatant.<br>
 +
8; Add the 500μL of New Wash and resuspend.<br>
 +
9; Centrifuge for 5 seconds at 15,000×g and 4°C.<br>
 +
10; Repeat wash (Steps 8-9).<br>
 +
11; Dry the pellet for 5-10 minutes under vacuum.<br>
 +
12. Add 20　μL of nuclease-free water and resuspend.<br>
 +
13. Centrifuge for 5 seconds at 15,000×g and 25°C.<br>
 +
14. Transfer supernatant including objective DNA into new tube.<br><br>
 +
 
 +
<h3>Ligation</h3><br>
 +
<h4>Ligation inset DNA and vector<br>
 +
DNA Ligation kit Ver 2.1(SolutionⅠ)/Takara<br></h4>
 +
1; Mix the insert DNA, vector and solution I (Table).<br>
 +
2; Incubation at 16°C for 30 minute.<br>
 +
3; Transform E. coli with ligation sample.<br>
 +
<br>
 +
<table border="1">
 +
<td width="150">reagent name</td>
 +
<td align="right" width="150">volume</td><tr>
 +
<td width="150">
 +
insert DNA<br>
 +
vector<br>
 +
solution I<br>
 +
</td>
 +
<td align="right" width="150">
 +
2 μL<br>
 +
2 μL<br>
 +
4 μL
 +
</td><tr>
 +
<td width="150">total</td>
 +
<td align="right" width="150">8 μL</td>
 +
</table>
 +
<br><br>
 +
 
 +
<h3>Colony PCR</h3><br>
 +
Confirmation of insert DNA in plasmid, directly doing PCR on <i>E. coli</i><br>
 +
1; Add 10 μL of reagent solution (Table 1) to PCR tube.<br>
 +
2; Pick up single colony from agar plate with tooth pick and sting replica plate (new LB agar plate).<br>
 +
3; Put and stir toothpick to reagent solution (Step 1).<br>
 +
4; Amplify insert DNA with PCR program (Table 2).<br>
 +
5; Electrophorese PCR sample with agar gel.<br>
 +
6; Check the band and length of insert DNA and decide the colony with insert DNA.<br>
 +
<br>
 +
<table border="1">
 +
<td width="350">reagent name</td>
 +
<td align="right" width="100">volume</td><tr>
 +
<td width="350">
 +
fowerd primer<br>
 +
reverse primer<br>
 +
Go taq® Green Master Mix(Promega)<br>
 +
MQ
 +
</td>
 +
<td align="right" width="100">
 +
0.5 μL<br>
 +
0.5 μL<br>
 +
5 μL<br>
 +
4 μL
 +
</td><tr>
 +
<td width="350">total</td>
 +
<td align="right" width="100">10 μL</td>
 +
</table>
 +
Table 1
 +
<br>
 +
 
 +
<table border="1">
 +
<td width="60"></td>
 +
<td width="100">Step 1</td>
 +
<td width="200">Step 2</td>
 +
<td width="120">Step 3</td><tr>
 +
<td width="60">Cycle</td>
 +
<td width="100">1</td>
 +
<td width="200">30</td>
 +
<td width="120">1</td><tr>
 +
<td width="60"></td>
 +
<td width="100" height="150" align="middle" valign="top">95℃<br>
 +
1:00</td>
 +
<td width="200" valign="top">
 +
&nbsp;&nbsp;&nbsp;
 +
95℃<br>
 +
&nbsp;&nbsp;&nbsp;
 +
0:10<br>
 +
&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
 +
72℃<br>
 +
&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
 +
55℃
 +
&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
 +
4:00<br>
 +
&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
 +
0:10
 +
</td>
 +
<td width="120" valign="top"><br><br>
 +
&nbsp;&nbsp;&nbsp;72℃<br>
 +
&nbsp;&nbsp;&nbsp;2：00<br><br><br><br>
 +
&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;4℃<br>
 +
&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;∞</td>
 +
</table>
 +
Table2<br><br>
 +
 
 +
<h3>Sequence analysis</h3>
 +
Identification of insert DNA<br>
 +
*Preparation of PCR product<br>
 +
Big Dye® Terminator Cycle Sequencing Kit Ver. 3.1 (Premix, Buffer) / Applied Biosystems<br>
 +
1; Add reagent solution (Table 1) to PCR tube and amplify insert DNA with PCR program<br> (Table2).
 +
 
 +
*Purification of PCR product and sequence analysis<br>
 +
Agencourt CleanSEQ® and 96 R ring Super Magnetic Plate® / Beckman Coulter<br>
 +
1; Add 10 μL of Agencourt CleanSEQ® 10 µL to PCR product.<br>
 +
2; Add 62 μL of 85% ethanol, mix and incubate for 3 minutes.<br>
 +
3; Incubate for 3 minutes on 96 R ring Super Magnetic Plate® and discard supernatant.<br>
 +
4; Add 100 μL of 85% ethanol and mix.<br>
 +
5; Incubate for 3 minutes on 96 R ring Super Magnetic Plate® and discard supernatant.<br>
 +
6; Repeat wash (Steps 4-5).<br>
 +
7; Dry for 10 minutes.<br>
 +
8; Add 40 μL nuclease-free water and mix.<br>
 +
9; Transfer 30μL of clear sample into a new plate for loading on the detector.<br>
 +
10; Load sample on sequencer and analyze.<br>
 +
<br>
 +
<table border="1">
 +
<td width="350">reagent name</td>
 +
<td align="right" width="100">volume</td><tr>
 +
<td width="350">
 +
plasmid<br>
 +
primer<br>
 +
premix<br>
 +
buffer<br>
 +
MQ
 +
</td>
 +
<td align="right" width="100">
 +
3 μL<br>
 +
0.5 μL<br>
 +
0.5 μL<br>
 +
4 μL<br>
 +
12 μL
 +
</td><tr>
 +
<td width="350">total</td>
 +
<td align="right" width="100">20 μL</td>
 +
</table><br>
 +
Table 1<br><br>
 +
 
 +
<table border="1">
 +
<td width="60"></td>
 +
<td width="100">Step 1</td>
 +
<td width="200">Step 2</td>
 +
<td width="120">Step 3</td><tr>
 +
<td width="60">Cycle</td>
 +
<td width="100">1</td>
 +
<td width="200">30</td>
 +
<td width="120">1</td><tr>
 +
<td width="60"></td>
 +
<td width="100" height="150" align="middle" valign="top">95℃<br>
 +
1:00</td>
 +
<td width="200" valign="top">
 +
&nbsp;&nbsp;&nbsp;
 +
95℃<br>
 +
&nbsp;&nbsp;&nbsp;
 +
0:10<br>
 +
&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
 +
60℃<br>
 +
&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
 +
50℃
 +
&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
 +
4:00<br>
 +
&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
 +
0:10
 +
</td>
 +
<td width="120" valign="top"><br><br>
 +
&nbsp;&nbsp;&nbsp;60℃<br>
 +
&nbsp;&nbsp;&nbsp;2：00<br><br><br><br>
 +
&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;4℃<br>
 +
&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;∞</td>
 +
</table><br>
 +
Table2
 +
 
 +
<br><br></tr>
</tr>
</tr>
<tr class="f-sp">
<tr class="f-sp">
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</table>
</div>
</div>
 +
<br><br><br>
 +
 +
</p>
 +
 +
 +
</body>
</body>
</html>
</html>

Latest revision as of 11:19, 5 October 2011

'''Protocols'''

Tokyo-NokoGen 2011

Department of Biotechnology and Life Science, Tokyo University of Agriculture and Technology

 

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Protocols

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Sponsors

Protocols

LB medium and LB agar gel Medium for cultivation of E. coli

LB medium (1 L)

1; Add about 900 mL of distilled water to beaker.
2; Add 25 g of LB medium, Miller(MERCK) and stir.
3; Add distilled water up to 1 L and take LB medium to media bottle.
4; Autoclave for 20 min at 120°C.

LB agar gel (1 L)

1; Prepare LB medium without autoclave (Steps 1-3 of 1L scale of LB medium).
2; Add 15 g of agar and stirrer bar.
3; Autoclave for 20 minutes at 120°C.
4; Stir and cool LB medium with agar, add appropriate antibiotic (table).
5; Pour LB medium (Step 4) in plate and cool down in clean bench.

f.c.
Ampicillin 100 μg/mL
Kanamycin 50 μg/mL
Chloramphenicol 30 μg/mL
Tetlacycline 11 μg/mL


Transformation

Inserting plasmid into E. coli

1; Incubate frozen competent cell (DH5α) on the ice for a few minutes.
2; Add 1~5 μL of plasmid to competent cell (DH5α) on the ice.
3; Incubate for 20 – 30 minutes on the ice.
4; Incubate for 45 seconds at 42°C.
5; Add 1 mL LB medium and cultivate for 1 hour at 37°C.
6; Spread culture medium on LB agar plate with appropriate antibiotic.

Plasmid extraction

Preparation of plasmid extracted from E. coli

1; Pick up single colony from agar plate and cultivate it in 1.5 mL LB medium containing appropriate antibiotic overnight at 37°C.
2; Move the culture medium to 1.5 mL tube.
3; Centrifuge for 5 seconds at 15,000×g and 4 °C and discard supernatant.
4; Add 100 μL Solution 1 to the pellet and resuspend and incubate for 3 minutes.
5; Add 100 μL Solution 2, invert tube gently 5 times and incubate for 3 minutes.
6; Add 100 μL Solution 3, invert tube 5 times and incubate for 3 minutes.
8; Add 200 μL Solution 4 and invert tube 5 times and centrifuge for 3 minutes at 15,000×g and 4 °C.
10; Take supernatant to new 1.5 mL tube and centrifuge for 3 minutes at 15,000×g and 4 °C.
11; Vortex Bind mix for 1 min and add 800 μL Bind mix to new 1.5 mL tube.
12; Add 400 μL supernatant after centrifugation (Step 10) to tube containing Bind mix (Step 11) and mix.
13; Incubate for 3 minutes, centrifuge for 3 seconds at 5,000×g and 4 °C, and discard supernatant.
14; Add 1 mL of 50% ethanol and resuspend.
15; Centrifuge for 3 seconds at 5,000×g and 4 °C and discard supernatant.
16; Repeat wash (Steps 14-15).
17; Dry pellet for a few minuet under a vacuum to remove residual ethanol.
18; Add 50 μL nuclease-free water or TE buffer and incubate for 3 minutes at 65°C.
19; Centrifuge for 3 minutes at 15,000×g and 4 °C.
19; 40 μL of supernatant into new 500 μL tube.

Restriction enzyme digestion of DNA

Cleavage of insert DNA from plasmid

1; Mix DNA and restriction enzyme (Table).
2; Incubate for 2 hours at 37°C.
3; Incubate for 10 minutes at 65°C.
4; Confirm the band of DNA by agar gel electrophoresis.


reagent name volume
DNA
restriction enzyme A
restriction enzyme B
buffre MQ		 5 μL
0.5 μL
0.5 μL
1.5 μL
7.5 μL
total 15 μL


Confirmation and separation of digested DNA

Preparation of agar gel

1; Add 1 g of agar to 100 mL of 1×TAE.
2; Boil and stir until solution is dissolved and clear.
3; Cool down, pour into container to set its shape.
4; Wait until gel dries.
5; Store gel in 1×TAE.


Agar gel electrophoresis

1; Place agar gel and pour 1×TAE in electrophoresis chamber.
2; Load DNA ladder and DNA sample mixed with loading dye on agar gel.
3; Electrophorese for 20 minutes at 100 V.
4; Stain gel by Sybr SafeTM Gel Stain (Invitrogen).
5; Visualize the band of DNA using UV light.
6; Confirm the length of digested DNA.

PCR

1; Add 25 μL of reagent solution (Table 1) to PCR tube.
2; Amplify target DNA with PCR program (Table 2).
3; Confirm the band of DNA by agar gel electrophoresis.

reagent name volume
primeSTAR® GXL DNA polymerase
5X GXL buffer
dNTP
template DNA
fowerd primer
reverse primer
MQ 		0.5 μL
5 μL
2 μL
1 μL
1 μL
1 μL
14.5 μL
total 25 μL
Table 1
Step 1 Step 2 Step 3
Cycle 1 30 1
98℃
1:00		     98℃
    0:10
                                    68℃
                  55℃            4:00
                  0:10

   68℃
   2：00



                4℃
                ∞
Table2

Gel purification

Purification of DNA from agar gel

GENECLEAN® II Kit(NaI、glass milk、NEW Wash)/Qbiogene

1; Cut the objective band in the agar gel after electrophoresis and stain with SYBR Safe.
2; Put the gel including objective DNA into 1.5 mL tube and measure the mass of that.
3; Add 2.5-3 fold volume NaI solution into the tube (Gel: NaI =1 mg : 1 μL ).
4; Incubate the gel at 50°C for 5 minute.
5; Add 10 μL of glass milk and vortex.
6; Incubate for 5 minutes and vortex per a minute.
7; Centrifuge for 5 seconds at 15,000×g and 4°C and discard the supernatant.
8; Add the 500μL of New Wash and resuspend.
9; Centrifuge for 5 seconds at 15,000×g and 4°C.
10; Repeat wash (Steps 8-9).
11; Dry the pellet for 5-10 minutes under vacuum.
12. Add 20　μL of nuclease-free water and resuspend.
13. Centrifuge for 5 seconds at 15,000×g and 25°C.
14. Transfer supernatant including objective DNA into new tube.

Ligation


Ligation inset DNA and vector
DNA Ligation kit Ver 2.1(SolutionⅠ)/Takara

1; Mix the insert DNA, vector and solution I (Table).
2; Incubation at 16°C for 30 minute.
3; Transform E. coli with ligation sample.

reagent name volume
insert DNA
vector
solution I
 2 μL
2 μL
4 μL
total 8 μL


Colony PCR


Confirmation of insert DNA in plasmid, directly doing PCR on E. coli
1; Add 10 μL of reagent solution (Table 1) to PCR tube.
2; Pick up single colony from agar plate with tooth pick and sting replica plate (new LB agar plate).
3; Put and stir toothpick to reagent solution (Step 1).
4; Amplify insert DNA with PCR program (Table 2).
5; Electrophorese PCR sample with agar gel.
6; Check the band and length of insert DNA and decide the colony with insert DNA.

reagent name volume
fowerd primer
reverse primer
Go taq® Green Master Mix(Promega)
MQ 		0.5 μL
0.5 μL
5 μL
4 μL
total 10 μL
Table 1
Step 1 Step 2 Step 3
Cycle 1 30 1
95℃
1:00		     95℃
    0:10
                                    72℃
                  55℃            4:00
                  0:10

   72℃
   2：00



                4℃
                ∞
Table2

Sequence analysis

Identification of insert DNA
*Preparation of PCR product
Big Dye® Terminator Cycle Sequencing Kit Ver. 3.1 (Premix, Buffer) / Applied Biosystems
1; Add reagent solution (Table 1) to PCR tube and amplify insert DNA with PCR program
(Table2). *Purification of PCR product and sequence analysis
Agencourt CleanSEQ® and 96 R ring Super Magnetic Plate® / Beckman Coulter
1; Add 10 μL of Agencourt CleanSEQ® 10 µL to PCR product.
2; Add 62 μL of 85% ethanol, mix and incubate for 3 minutes.
3; Incubate for 3 minutes on 96 R ring Super Magnetic Plate® and discard supernatant.
4; Add 100 μL of 85% ethanol and mix.
5; Incubate for 3 minutes on 96 R ring Super Magnetic Plate® and discard supernatant.
6; Repeat wash (Steps 4-5).
7; Dry for 10 minutes.
8; Add 40 μL nuclease-free water and mix.
9; Transfer 30μL of clear sample into a new plate for loading on the detector.
10; Load sample on sequencer and analyze.

reagent name volume
plasmid
primer
premix
buffer
MQ 		3 μL
0.5 μL
0.5 μL
4 μL
12 μL
total 20 μL

Table 1

Step 1 Step 2 Step 3
Cycle 1 30 1
95℃
1:00		     95℃
    0:10
                                    60℃
                  50℃            4:00
                  0:10

   60℃
   2：00



                4℃
                ∞

Table2




Retrieved from "http://2011.igem.org/Team:Tokyo-NoKoGen/protocols"