Fix BamI sticky end in PstI+BamHI step of I27-synthesis post.

[blog.git] / posts / I27-synthesis.mdwn

diff --git a/posts/I27-synthesis.mdwn b/posts/I27-synthesis.mdwn
index 236a996b60401748a9bb6982bb242c39f868e522..e5eb42e53a110dd44f3fd9a4b42ada9a6f66181d 100644 (file)
--- a/posts/I27-synthesis.mdwn
+++ b/posts/I27-synthesis.mdwn
@@ -204,7 +204,7 @@ The single-SP plasmid, pSP4-1, is split in two parallel reactions.
 #### PstI + BamHI
 
         G...AGATCT-SP-G
-    ACGTC...TCTAGA-SP-CCTAGG
+    ACGTC...TCTAGA-SP-CCTAG
 
 #### PstI + BglII
 
@@ -282,7 +282,7 @@ vector", but I'm not sure why they would need a non-expression vector,
 as they don't reference cross-vector subcloning after inserting their
 I27 monomer into the plasmid.
 
-From the [Qiagen site][pQE30], the section around the linker
+From the [Qiagen site][pQE30-b], the section around the linker
 nucleotides 115 through 203 is:
 
         ,RGS-His epitope__________________. ,BamHI.