Team:UNIPV-Pavia/Methods Materials/LB

From 2009.igem.org

(Difference between revisions)
Line 38: Line 38:
<br>
<br>
<br>
<br>
-
<table width='100%'><tr><td>
+
<table width='80%'><tr><td>
*For a final volume of 1 l, put:
*For a final volume of 1 l, put:
**10 g NaCl
**10 g NaCl
Line 53: Line 53:
*Cover and store at +4°C.
*Cover and store at +4°C.
*Always check for contaminations before using!
*Always check for contaminations before using!
-
<br></td><td align='right'>
+
<br></td><td align='right' valign='top'>
<div align='right'>
<div align='right'>
-
<table size='30%' >
+
<table size='30%'>
<tr><td bgcolor='red'>'''Materials needed:'''
<tr><td bgcolor='red'>'''Materials needed:'''
*'''NaCl'''
*'''NaCl'''

Revision as of 14:23, 25 June 2009

EthanolPVanimation.gif



Protocols



LB medium

(Estimated time: 10 min + 4 hours of autoclavation and cooling)

  • For a final volume of 1 l, put:
    • 10 g NaCl
    • 10 g BactoTryptone
    • 5 g Yeast extract
    • 15 g Agar (only for LB plates)
  • into 1 l of ddH2O.
  • Autoclave the solution.
  • Let it cool to ~40-45°C
  • Add the proper antibiotic if needed.
  • ONLY FOR PLATES:
    • Pour an homogenous layer of agar LB into Petri plates under the hood.
    • Let agar LB polymerase.
  • Cover and store at +4°C.
  • Always check for contaminations before using!

Materials needed:
  • NaCl
  • BactoTryptone
  • Yeast extract
  • ddH2O
  • Agar
  • Clean bottle or E-flask


Retrieved from "http://2009.igem.org/Team:UNIPV-Pavia/Methods_Materials/LB"