Line 11: | Line 11: | ||
<body> | <body> | ||
<div class="all"> | <div class="all"> | ||
− | + | <header> | |
− | + | <nav class="navbar navbar-default navbar-inverse navbar-fixed-top"> | |
− | + | <div class="container"> | |
− | + | <ul> | |
− | + | <li><a href="https://2018.igem.org/Team:CCU_Taiwan">Home</a> | |
− | + | <ul> | |
− | + | <li><a href="#">Our team</a></li> | |
− | + | <li><a href="#">Resourses</a></li> | |
− | + | </ul> | |
− | + | </li> | |
− | + | <li><a href="#">Parts</a></li> | |
− | + | <li><a href="#">Modeling</a> | |
− | + | <ul> | |
− | + | <li><a href="https://2018.igem.org/Team:CCU_Taiwan/Model">Overview</a></li> | |
− | + | </ul> | |
− | + | </li> | |
− | + | <li><a href="#">Project</a> | |
− | + | <ul> | |
− | <li><a href="#"> | + | <li><a href="https://2018.igem.org/Team:CCU_Taiwan/InterLab">Interlab</a></li> |
− | + | <li><a href="https://2018.igem.org/Team:CCU_Taiwan/Project/Protocol">Protocol</a></li> | |
− | + | <li><a href="https://2018.igem.org/Team:CCU_Taiwan/Notebook">Notebook</a></li> | |
− | + | </ul> | |
− | + | </li> | |
− | + | <li><a href="#">Result</a></li> | |
− | + | <li><a href="#">Human Practice</a></li> | |
+ | <li><a href="#">Medals</a></li> | ||
+ | </ul> | ||
+ | </div> | ||
+ | </nav> | ||
+ | </header> | ||
<div <div class="interlab">> | <div <div class="interlab">> | ||
<p class="first"> Transform (homemade E-coli DH5α)</p> | <p class="first"> Transform (homemade E-coli DH5α)</p> |
Revision as of 18:20, 21 July 2018
Transform (homemade E-coli DH5α)
1. Take competent cells out of -80°C and thaw on ice (approximately 20-30 mins).
2.Remove agar plates (containing the appropriate antibiotic) from storage at 4°C and let warm up to room temperature and then (optional) incubate in 37°C incubator.
3.Mix 5 μl of DNA into 50 μL of competent cells in a microcentrifuge or falcon tube. GENTLY mix by flicking the bottom of the tube with your finger a few times.
4.Incubate the competent cell/DNA mixture on ice for 30 mins.
5.Heat shock each transformation tube into a 42°C water bath for 90 secs.
6.Put the tubes back on ice for 5 min.
7.Add 50 μl LB to the bacteria and grow in 37°C shaking incubator for 180 min.
8.Spin down
9.Plate all of the transformation onto a 10 cm LB agar plate containing the appropriate antibiotic (Chloramphenicol).
10.Incubate plates at 37°C overnight.