Double Digest Guide

From 2006.igem.org

(Difference between revisions)
Jump to: navigation, search
(iGEM Double Digest Guide)
Line 2: Line 2:
-
[[Image:BioBricks_from_paper.png]]
+
{| width="800px" cellspacing="0"
 +
|- valign="top"
 +
| style="width:180px" | '''Standard BioBrick Cloning Sites''' (Knight)
 +
| style="background:lightgrey"|<font face="courier">5'--GAATTC GCGGCCGC T TCTAGA G ----insert---- T ACTAGT A GCGGCCG CTGCAG--<br>3'--CTTAAG CGCCGGCG A AGATCT C -------------- A TGATCA T CGCCGGC GACGTC--</font>
 +
|- valign="top"
 +
| style="width:180px" | <font color="white">...</font>
 +
| style="background:lightgrey"|<font face="courier"><font color="lightgrey">5'--<font color="black">EcoRI</font>- --<font color="black">NotI</font>-- - -<font color="black">XbaI</font>- - -------------- T -<font color="black">SpeI</font>- - -<font color="black">NotI</font>-- -<font color="black">PstI</font>---</font>
 +
|}
Line 28: Line 35:
'''Promega® Buffer H''' [90 mM Tris-HCl pH 7.5, 10 mM MgCl2, 50 mM NaCl]
'''Promega® Buffer H''' [90 mM Tris-HCl pH 7.5, 10 mM MgCl2, 50 mM NaCl]
-
 
-
 
===References===
===References===
* [https://dspace.mit.edu/handle/1721.1/21168:Knight, Tom. Idempotent Vector Design for Standard Assembly of Biobricks]
* [https://dspace.mit.edu/handle/1721.1/21168:Knight, Tom. Idempotent Vector Design for Standard Assembly of Biobricks]

Revision as of 21:49, 7 November 2006

===iGEM Double Digest Guide=== by Karmella Haynes, 2006


Standard BioBrick Cloning Sites (Knight) 5'--GAATTC GCGGCCGC T TCTAGA G ----insert---- T ACTAGT A GCGGCCG CTGCAG--
3'--CTTAAG CGCCGGCG A AGATCT C -------------- A TGATCA T CGCCGGC GACGTC--
... 5'--EcoRI- --NotI-- - -XbaI- - -------------- T -SpeI- - -NotI-- -PstI---


Enzymes Buffer Temperature Purpose
EcoRI, XbaI Low 37°C To create a "Front Vector"
EcoRI, SpeI Low 37°C To create a "Front Insert"
SpeI, PstI Medium 37°C To create a "Back Vector"
XbaI, PstI Low 37°C To create a "Back Insert"
EcoRI, PstI Promega® Buffer H 37°C To excise entire insert or validate part size


Davidson Buffers [10 mM Tris-HCl pH 7.5, 10 mM MgCl2, 0.1 mg/mL BSA, X mM NaCl]

  • 0 (zero), 0 NaCl
  • Low, 50 mM NaCl
  • Medium, 100 mM NaCl
  • High, 150 mM NaCl

Promega® Buffer H [90 mM Tris-HCl pH 7.5, 10 mM MgCl2, 50 mM NaCl]

References

Personal tools
Past/present/future years