Team:Biwako Nagahama/general protocol

From 2013.igem.org

(Difference between revisions)
(Genaral protocol)
(Genaral protocol)
Line 20: Line 20:
</table>
</table>
</div>
</div>
-
<p>dH2O・・・12.7μL</p>
 
-
<p>10×NH4 buffer・・・2.5μL</p>
 
-
<p>50mM MgCl2・・・0.75μL</p>
 
-
<p>25mM dNTPs・・・2μL</p>
 
-
<p>10μM F Primer・・・1μL</p>
 
-
<p>10μM R Primer・・・1μL</p>
 
-
<p>BIO Taq(5U/μL)・・・0.05μL</p>
 
-
<p>Template(<500ng)・・・5μL</p>
 
-
<p>Total・・・25μL</p>
 
-
<p>[https://www.bioline.com/h_prod_detail.asp?itemid=219 BIOTAQ™ DNA Polymerase]</p>
 
-
<p>↓</p>
 
----
----
<p>95℃ 30sec</p>
<p>95℃ 30sec</p>

Revision as of 18:25, 27 September 2013

Contents

Genaral protocol

BIOTAQ™ DNA PolymerasePCR

dH2O12.7μL
10×NH4 buffer2.5μL
50mM MgCl20.75μL
25mM dNTPs2μL
10μM F Primer1μL
10μM R Primer1μL
BIO Taq(5U/μL)0.05μL
Template(<500ng)5μL
Total25μL

95℃ 30sec

95℃ 10sec

55℃ 20sec 30cycles

72℃ 2min

72℃ 2min

10℃ ∞



Distribution kit


↓With a pipette tip, punch a hole in the foil

↓Add 10μL of dH2O,and pipetting

↓Put 5min

↓Pipette 1uL of the resuspended DNA Transformation into your desired 100μL of competent cells

↓Hold on ice for 20min

↓Heat shock at 42℃ for 30sec

↓quickly

↓On ice for 2min

↓Add 900μL of SOCborth

↓Hold at 37℃ for 30min

↓Plating 100μL of DNA Transformation

↓Centrifuge for 1 min(13,000rpm)

↓Waste supernatant for 800μL, and pipetting

↓Plating all

↓Incubate at 37℃ (over night)


Phenol-chloroform extraction


Add Phenol-chloroform where is equivalent to Exo Star process sample

↓Centrifuge 4℃ 13,000rpm 5min

Only supernatant was taken


EtOH crystalization


↓Add 1μL 20mg/mL Glycogen

↓Mix

↓Add 1/10 volume 3M CH3COONa(pH5.2)

↓Add 2.5 times volume 99.5% EtOH

↓Vortex

↓Centrifuge 4℃ 13,000rpm 20min

↓Waste supernatant

↓Add 500μL 70% EtOH

↓Mix

↓Centrifuge for 10s in a table-top microcentrifuge

↓Waste supernatant

↓65℃ Dry up

↓Add 11μL TE buffer