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/**************** Protocols details *****************/ | /**************** Protocols details *****************/ | ||
− | #lb_broth, #lb_agar, #chloramphenicol, #petri_dish, #glycerol, #cacl2, #mgcl2, #sucrose, #iptg, #res { | + | #lb_broth, #lb_agar, #chloramphenicol, #petri_dish, #glycerol, #cacl2, #mgcl2, #sucrose, #iptg, #res, #competentbacteria, #electrophorese, #bacterialtransfo, #minimaxiprep, #pcr, #probeinsertion, #plasmidactivation, #purification, #plasmiddrying, #bacterialyoph { |
display: none; | display: none; | ||
width: 100%; | width: 100%; | ||
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} | } | ||
− | #lb_broth:target, #lb_agar:target, #chloramphenicol:target, #petri_dish:target, #glycerol:target, #cacl2:target, #mgcl2:target, #sucrose:target, #iptg:target, #res:target { | + | #lb_broth:target, #lb_agar:target, #chloramphenicol:target, #petri_dish:target, #glycerol:target, #cacl2:target, #mgcl2:target, #sucrose:target, #iptg:target, #res:target, #competentbacteria:target, #electrophorese:target, #bacterialtransfo:target, #minimaxiprep:target, #pcr:target, #probeinsertion:target, #plasmidactivation:target, #purification:target, #plasmiddrying:target, #bacterialyoph:target { |
display: block; | display: block; | ||
-webkit-animation: fadeIn 1s; | -webkit-animation: fadeIn 1s; | ||
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<div style="width:100%; margin: 1% 0%;"><center> | <div style="width:100%; margin: 1% 0%;"><center> | ||
− | <a href="#" style="text-decoration: none;"> <img class="logo" src="https://static.igem.org/mediawiki/2017/0/06/Lab_2.png"></a> | + | <a href="#competentbacteria" style="text-decoration: none;"> <img class="logo" src="https://static.igem.org/mediawiki/2017/0/06/Lab_2.png"></a> |
− | <a href="#" style="text-decoration: none;"> <img class="logo" src="https://static.igem.org/mediawiki/2017/0/06/Lab_2.png"></a> | + | <a href="#electrophorese" style="text-decoration: none;"> <img class="logo" src="https://static.igem.org/mediawiki/2017/0/06/Lab_2.png"></a> |
− | <a href="#" style="text-decoration: none;"> <img class="logo" src="https://static.igem.org/mediawiki/2017/0/06/Lab_2.png"></a> | + | <a href="#bacterialtransfo" style="text-decoration: none;"> <img class="logo" src="https://static.igem.org/mediawiki/2017/0/06/Lab_2.png"></a> |
− | <a href="#" style="text-decoration: none;"> <img class="logo" src="https://static.igem.org/mediawiki/2017/0/06/Lab_2.png"></a> | + | <a href="#minimaxiprep" style="text-decoration: none;"> <img class="logo" src="https://static.igem.org/mediawiki/2017/0/06/Lab_2.png"></a> |
− | <a href="#" style="text-decoration: none;"> <img class="logo" src="https://static.igem.org/mediawiki/2017/0/06/Lab_2.png"></a> | + | <a href="#pcr" style="text-decoration: none;"> <img class="logo" src="https://static.igem.org/mediawiki/2017/0/06/Lab_2.png"></a> |
− | <a href="#" style="text-decoration: none;"> <img class="logo" src="https://static.igem.org/mediawiki/2017/0/06/Lab_2.png"></a> | + | <a href="#probeinsertion" style="text-decoration: none;"> <img class="logo" src="https://static.igem.org/mediawiki/2017/0/06/Lab_2.png"></a> |
− | <a href="#" style="text-decoration: none;"> <img class="logo" src="https://static.igem.org/mediawiki/2017/0/06/Lab_2.png"></a> | + | <a href="#plasmidactivation" style="text-decoration: none;"> <img class="logo" src="https://static.igem.org/mediawiki/2017/0/06/Lab_2.png"></a> |
− | <a href="#" style="text-decoration: none;"> <img class="logo" src="https://static.igem.org/mediawiki/2017/0/06/Lab_2.png"></a> | + | <a href="#purification" style="text-decoration: none;"> <img class="logo" src="https://static.igem.org/mediawiki/2017/0/06/Lab_2.png"></a> |
− | <a href="#" style="text-decoration: none;"> <img class="logo" src="https://static.igem.org/mediawiki/2017/0/06/Lab_2.png"></a> | + | <a href="#plasmiddrying" style="text-decoration: none;"> <img class="logo" src="https://static.igem.org/mediawiki/2017/0/06/Lab_2.png"></a> |
− | <a href="#" style="text-decoration: none;"> <img class="logo" src="https://static.igem.org/mediawiki/2017/0/06/Lab_2.png"></a> | + | <a href="#bacterialyoph" style="text-decoration: none;"> <img class="logo" src="https://static.igem.org/mediawiki/2017/0/06/Lab_2.png"></a> |
</center></div> | </center></div> | ||
Revision as of 12:58, 31 August 2017
Protocols
Preparations
LB Broth
Materials
Methods
- Add 20g of LB Broth Base per 1L of distillated water
- Homogenize
- Autoclave at 121°C for 15 minutes
CLOSE
LB Agar
Materials
Methods
- Add 32g of LB Agar per 1L of distilled water
- Homogenize
- Autoclave at 121°C for 15 minutes
CLOSE
Chloramphenicol (Cam) 25ug/mL Stock
Materials
Methods
- Add 0,25g of Cam per 10mL of ethanol
- Homogenize by vortexing
- Filter with a 22mm membrane filter
- Conserve at -20°C in 1mL aliquot
CLOSE
Petri Dish Preparation
Materials
Methods
- Add of 20uL Cam in 20mL of liquid LB Agar
- Pour the solution in the plate
- Wait until the agar solidifies
- Conserve returned in 4°C
CLOSE
Glycerol 80%
Materials
Methods
- Harvest 80mL of glycerol 100%
- Add 20mL of sterile water
- Conserve at 4°C
CLOSE
CaCl2 100mM
Materials
Methods
- Dissolve 0,056g of CaCl2 in 5mL of sterile water
- Conserve at 4°C
CLOSE
MgCl2 100mM
Materials
Methods
- Dissolve 0,6105g of MgCl2 in 30mL of sterile water
- Conserve at 4°C
CLOSE
Sucrose 100mM
Materials
Methods
- Dissolve 0,171g of sucrose in 5mL of sterile water
- Conserve at 4°C
CLOSE
IPTG 4mM
Materials
Methods
- Add 10µL of Cam in 10mL of LB
- Homogenize
- Remove 90µL of solution and add 80µL of IPTG
- Conserve at -20°C
CLOSE
Resuspension Solution for Lyophilized Bacteria
Materials
Materials
Methods
- Add 350µL of DMSO and 1,5µL of 2-mercaptoethanol in 5mL of sterile water
- Conserve at 4°C
CLOSE
Experimentations