Difference between revisions of "HPP New Start and Finish"

From GcatWiki
Jump to: navigation, search
(Created page with 'July 23, 2011 New Oligos to Order START_TOP (67 nt) AATTCGGTCTCAGACGTTGACGGCTAGCTCAGTCCTAGGTACAGTGCTAGCGTGGAGAGACGCTGCA START_Bot (59 nt) GCGTCTCTCCACGCTAGCACTGTACCTAGGACTGAGC…')
 
Line 1: Line 1:
 
July 23, 2011
 
July 23, 2011
New Oligos to Order
+
New Oligos to Order <br>
 
START_TOP (67 nt)
 
START_TOP (67 nt)
  
Line 16: Line 16:
  
 
GGGTCTCTCTCGACTGATGCCCACTGAGACGG
 
GGGTCTCTCTCGACTGATGCCCACTGAGACGG
 +
 
NewHPPVec_Top (36 nt)
 
NewHPPVec_Top (36 nt)
 
AATTCGTCCAGAGACCGCTAGCGGTCTCACGAGCTGCA
 
AATTCGTCCAGAGACCGCTAGCGGTCTCACGAGCTGCA
  
 
NewHPPVec_Bot (32 nt)
 
NewHPPVec_Bot (32 nt)
GCTCGTGAGACCGCTAGCGGTCTCTGGACG
+
GCTCGTGAGACCGCTAGCGGTCTCTGGACG<br>
  
New START Half Edge
+
'''New START Half Edge'''
 
1. Use BsaI to free up new START word (GTCC) on 5’ end that allows ligation to new HPP vector.
 
1. Use BsaI to free up new START word (GTCC) on 5’ end that allows ligation to new HPP vector.
 
2. Use BsmBI to free up half-edge word (GTGG) on 3’ end that allows ligation to any Gene1 half-edge.
 
2. Use BsmBI to free up half-edge word (GTGG) on 3’ end that allows ligation to any Gene1 half-edge.
 
3. In between these is a J23100 promoter.
 
3. In between these is a J23100 promoter.
4. Flanked by EcoRI and PstI sticky ends for cloning.
+
4. Flanked by EcoRI and PstI sticky ends for cloning.<br><br>
 +
 
 
  RI  BsaI>  /START        J23100                    /Half  <BsmBI PstI
 
  RI  BsaI>  /START        J23100                    /Half  <BsmBI PstI
 
AATTC GGTCTC A GTCC TTGACGGCTAGCTCAGTCCTAGGTACAGTGCTAGC GTGG A GAGACG CTGCA
 
AATTC GGTCTC A GTCC TTGACGGCTAGCTCAGTCCTAGGTACAGTGCTAGC GTGG A GAGACG CTGCA
 
     G CCAGAG T CAGG AACTGCCGATCGAGTCAGGATCCATGTCACGATCG CACC T CTCTGC G
 
     G CCAGAG T CAGG AACTGCCGATCGAGTCAGGATCCATGTCACGATCG CACC T CTCTGC G
 
                   /                                        /
 
                   /                                        /
BsaI
+
<br><br>
 
BsmBI
 
 
   
 
   
New FINISH Half Edge
+
'''New FINISH Half Edge'''
 
1. Use BsmBI to free up half-edge word (GTGG) on 5’ end that allows ligation to any Gene2 half-edge.
 
1. Use BsmBI to free up half-edge word (GTGG) on 5’ end that allows ligation to any Gene2 half-edge.
 
2. Use BsaI to free up new FINISH word (CGAG) on 3’ end that allows ligation to new tr5f4HPP vector.
 
2. Use BsaI to free up new FINISH word (CGAG) on 3’ end that allows ligation to new tr5f4HPP vector.
 
3. In between these is a 8 nt spacer.
 
3. In between these is a 8 nt spacer.
4. Flanked by EcoRI and PstI sticky ends for cloning.
+
4. Flanked by EcoRI and PstI sticky ends for cloning.<br><br>
 +
 
 
  RI  BsmBI>  /Half  Spacer  /FINISH  <BsaI  PstI
 
  RI  BsmBI>  /Half  Spacer  /FINISH  <BsaI  PstI
 
AATTC CGTCTC A  GTGG  GCATCAGT  CGAG  A GAGACC CTGCA
 
AATTC CGTCTC A  GTGG  GCATCAGT  CGAG  A GAGACC CTGCA
 
     G GCAGAG T  CACC  CGTAGTCA  GCTC  T CTCTGG G
 
     G GCAGAG T  CACC  CGTAGTCA  GCTC  T CTCTGG G
 
                                             /                                /
 
                                             /                                /
New HPP Vector
+
'''New HPP Vector'''
 
1. Use BsaI to free up a new START word and a new FINISH word that are different from any of the Gene words (listed below).
 
1. Use BsaI to free up a new START word and a new FINISH word that are different from any of the Gene words (listed below).
 
2. NheI site in the middle for cloning in any XbaI/SpeI BioBrick fragment, such as the ccdB Death Gene or a reporter expression cassette.
 
2. NheI site in the middle for cloning in any XbaI/SpeI BioBrick fragment, such as the ccdB Death Gene or a reporter expression cassette.
 
3. Flanked by EcoRI and PstI sticky ends.
 
3. Flanked by EcoRI and PstI sticky ends.
 +
 +
'''Specific Words Used So Far'''
 
START GTCC  GGAC
 
START GTCC  GGAC
 
FINISH CGAG  CTCG
 
FINISH CGAG  CTCG
Line 58: Line 61:
 
ilvE GGGG  CCCC
 
ilvE GGGG  CCCC
 
CAT CGGT  ACCG
 
CAT CGGT  ACCG
TyrB CGCA  TGCG
+
TyrB CGCA  TGCG<br>
 +
 
 
   RI  / START    <BsaI    NheI    BsaI>    / FINISH  PstI
 
   RI  / START    <BsaI    NheI    BsaI>    / FINISH  PstI
 
AATTC  GTCC  A GAGACC GCTAGC GGTCTC A  CGAG  CTGCA
 
AATTC  GTCC  A GAGACC GCTAGC GGTCTC A  CGAG  CTGCA
 
     G  CAGG  T CTCTGG CGATCG CCAGAG T  GCTC  G
 
     G  CAGG  T CTCTGG CGATCG CCAGAG T  GCTC  G
 
               /                                    /
 
               /                                    /

Revision as of 20:10, 27 July 2011

July 23, 2011 New Oligos to Order
START_TOP (67 nt)

AATTCGGTCTCAGACGTTGACGGCTAGCTCAGTCCTAGGTACAGTGCTAGCGTGGAGAGACGCTGCA

START_Bot (59 nt)

GCGTCTCTCCACGCTAGCACTGTACCTAGGACTGAGCTAGCCGTCAACGTCTGAGACCG

FINISH_Top (40 nt)

AATTCCGTCTCAGTGGGCATCAGTCGAGAGAGACCCTGCA

FINISH_Bot (32 nt)

GGGTCTCTCTCGACTGATGCCCACTGAGACGG

NewHPPVec_Top (36 nt) AATTCGTCCAGAGACCGCTAGCGGTCTCACGAGCTGCA

NewHPPVec_Bot (32 nt) GCTCGTGAGACCGCTAGCGGTCTCTGGACG

New START Half Edge 1. Use BsaI to free up new START word (GTCC) on 5’ end that allows ligation to new HPP vector. 2. Use BsmBI to free up half-edge word (GTGG) on 3’ end that allows ligation to any Gene1 half-edge. 3. In between these is a J23100 promoter. 4. Flanked by EcoRI and PstI sticky ends for cloning.

RI   BsaI>   /START         J23100                    /Half   <BsmBI PstI

AATTC GGTCTC A GTCC TTGACGGCTAGCTCAGTCCTAGGTACAGTGCTAGC GTGG A GAGACG CTGCA

   G CCAGAG T CAGG AACTGCCGATCGAGTCAGGATCCATGTCACGATCG CACC T CTCTGC G
                  /                                        /



New FINISH Half Edge 1. Use BsmBI to free up half-edge word (GTGG) on 5’ end that allows ligation to any Gene2 half-edge. 2. Use BsaI to free up new FINISH word (CGAG) on 3’ end that allows ligation to new tr5f4HPP vector. 3. In between these is a 8 nt spacer. 4. Flanked by EcoRI and PstI sticky ends for cloning.

RI   BsmBI>   /Half  Spacer   /FINISH   <BsaI  PstI

AATTC CGTCTC A GTGG GCATCAGT CGAG A GAGACC CTGCA

   G GCAGAG T  CACC  CGTAGTCA   GCTC  T CTCTGG G
                                           /                                 /

New HPP Vector 1. Use BsaI to free up a new START word and a new FINISH word that are different from any of the Gene words (listed below). 2. NheI site in the middle for cloning in any XbaI/SpeI BioBrick fragment, such as the ccdB Death Gene or a reporter expression cassette. 3. Flanked by EcoRI and PstI sticky ends.

Specific Words Used So Far START GTCC GGAC FINISH CGAG CTCG Half-Edge GTGG CCAC GFP GGGT ACCC RFP CTGC GCAG LacZ CCTG CAGG AspC CGTC GACG PyrE GGCG CGCC ilvE GGGG CCCC CAT CGGT ACCG TyrB CGCA TGCG

 RI   / START    <BsaI    NheI     BsaI>     / FINISH  PstI

AATTC GTCC A GAGACC GCTAGC GGTCTC A CGAG CTGCA

   G  CAGG  T CTCTGG CGATCG CCAGAG T  GCTC  G
             /                                     /