User:Karmella Haynes/Notebook/BioBrick cloning/2013/01/05: Difference between revisions

From OpenWetWare
Jump to navigationJump to search
(fix raw html notebook nav)
 
(22 intermediate revisions by one other user not shown)
Line 2: Line 2:
|-
|-
|style="background-color: #EEE"|[[Image:owwnotebook_icon.png|128px]]<span style="font-size:22px;">Karmella's BioBrick Cloning</span>
|style="background-color: #EEE"|[[Image:owwnotebook_icon.png|128px]]<span style="font-size:22px;">Karmella's BioBrick Cloning</span>
|style="background-color: #F2F2F2" align="center"|<html><img src="/images/9/94/Report.png" border="0" /></html> [[{{#sub:{{FULLPAGENAME}}|0|-11}}|Main project page]]<br />{{#if:{{#lnpreventry:{{FULLPAGENAME}}}}|<html><img src="/images/c/c3/Resultset_previous.png" border="0" /></html>[[{{#lnpreventry:{{FULLPAGENAME}}}}{{!}}Previous entry]]<html>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</html>}}{{#if:{{#lnnextentry:{{FULLPAGENAME}}}}|[[{{#lnnextentry:{{FULLPAGENAME}}}}{{!}}Next entry]]<html><img src="/images/5/5c/Resultset_next.png" border="0" /></html>}}
|style="background-color: #F2F2F2" align="center"|[[File:Report.png|frameless|link={{#sub:{{FULLPAGENAME}}|0|-11}}]][[{{#sub:{{FULLPAGENAME}}|0|-11}}|Main project page]]<br />{{#if:{{#lnpreventry:{{FULLPAGENAME}}}}|[[File:Resultset_previous.png|frameless|link={{#lnpreventry:{{FULLPAGENAME}}}}]][[{{#lnpreventry:{{FULLPAGENAME}}}}{{!}}Previous entry]]&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;}}{{#if:{{#lnnextentry:{{FULLPAGENAME}}}}|[[{{#lnnextentry:{{FULLPAGENAME}}}}{{!}}Next entry]][[File:Resultset_next.png|frameless|link={{#lnnextentry:{{FULLPAGENAME}}}}]]}}
|-
|-
| colspan="2"|
| colspan="2"|
Line 8: Line 8:
==01/05/13==
==01/05/13==
<!-- Precede finished items with a checkmark &#x2713; -->
<!-- Precede finished items with a checkmark &#x2713; -->
* Golden gate: PCR parts, complete protocol for Brady's construct
* Gibson: PCR parts, complete protocol for Brady's construct
* Gibson: PCR parts, complete protocol for Brady's construct
* Golden gate: PCR parts; waiting on BsmBI from NEB




Line 19: Line 19:


'''PCR'''
'''PCR'''
# V0120, Gib_BBS F / Gib_BBP R
# V0120, Gib_BBS F (Gib0001) / Gib_BBP R (Gib0002)
# pSB1A3, Gib_BBS F / Gib_BBP R
# pSB1A3, Gib_BBS F (Gib0001) / Gib_BBP R (Gib0002)
# hPCD, ## / ##
# hPCD, BBP-hPCD fwd (BL9) / hPCD-BL01 rev (BL7)
# BL01, ## / ##
# BL01, hPCD-BL01 fwd (BL8) / BL01-BBS rev (BL10)


{| {{table}} border="1" cellspacing="3" <!-- Digest check rxn. table -->
{| {{table}} border="1" cellspacing="3" <!-- Digest check rxn. table -->
Line 28: Line 28:
| bgcolor=#cfcfcf | Reagent
| bgcolor=#cfcfcf | Reagent
| bgcolor=#cfcfcf | Volume  
| bgcolor=#cfcfcf | Volume  
| rowspan="7" | <u>Expected:</u><br>1. V0120 = size<br>2. pSB1A3 = size<br>3. hPCD = size<br>4. BL01 = size
| rowspan="7" | <u>Expected:</u><br>G1. V0120 = 3200<br>G2. pSB1A3 = 2000<br>G3. hPCD = 186<br>G4. BL01 = 2520
| rowspan="7" | <!-- [[Image:GelImage.jpg|400px|Hover name]]<br>15 μL/lane; 1% agarose; [http://openwetware.org/wiki/Image:KAH_Fermentas_GeneRuler_1kbplus.jpg Ladder] -->
| rowspan="7" | [[Image:KAH010513_gel1.jpg|300px|PCR gel]]<br>10 μL/lane; 1% agarose; [http://openwetware.org/wiki/Image:KAH_Fermentas_GeneRuler_1kbplus.jpg Ladder]
|-
|-
| DNA(plasmid) || 0.5 μL
| DNA(plasmid) || 0.5 μL
Line 39: Line 39:
| 2x GoTaq mix || 25.0
| 2x GoTaq mix || 25.0
|-
|-
| dH<sub>2</sub>O || ##
| dH<sub>2</sub>O || 22.5
|-
|-
| &nbsp; || 50 μL  
| &nbsp; || 50 μL  
Line 48: Line 48:
* 72°C, 3 min.
* 72°C, 3 min.
* 4°C, ∞
* 4°C, ∞
'''Purification'''
* Cleaned remaining 40 μL of PCR using the Zymo DNA Clean & Concentrator kit
* Eluted samples with 20 μL dH<sub>2</sub>O
'''DNA Concentrations'''
{| {{table}} border="1" cellspacing="3" <!-- Digest check rxn. table -->
|- valign="top"
| bgcolor=#cfcfcf | Sample
| bgcolor=#cfcfcf | OD 260
| bgcolor=#cfcfcf | 260/ 280
| bgcolor=#cfcfcf | ng/μL
|-
| G1 V0120 || 0.108 || 1.801 || 108.375
|-
| G2 pSB1A3 || 0.101 || 1.849 || 100.553
|-
| G3 hPCD || 0.034 || 1.876 || 33.586
|-
| G4 BL01 || 0.113 || 1.828 || 112.79
|}
'''Reaction set-up'''
* Use 0.2 - 0.5 pmol, per NEB's suggestion, [http://www.neb.com/nebecomm/products/protocol819.asp]
* pmols = ng x 1000 / bp x 650 daltons; ng = (pmols x bp x 650 daltons) / 1000
* Total volume of DNA = 5.0 μL max
1. hPCD + BL01 + V0120
* vector V0120, 0.1 pmol = 208 ng = 1.9 μL (use 1.4 μL)
* 2:1 insert hPCD, 0.2 pmol = 24 ng = 0.7 μL
* 2:1 insert BL01, 0.2 pmol = 328 ng = 2.9 μL
2. hPCD + BL01 + V0120
* vector pSB1A3, 0.1 pmol = 130 ng = 1.3 μL
* 2:1 insert hPCD, 0.2 pmol = 24 ng = 0.7 μL (use 0.8 μL)
* 2:1 insert BL01, 0.2 pmol = 328 ng = 2.9 μL
Gibson reactions:
# hPCD + BL01 + V0120
# V0120
# hPCD + BL01 + pSB1A3
# pSB1A3
{| {{table}} border="1" cellspacing="3" <!-- Digest check rxn. table -->
|- valign="top"
| bgcolor=#cfcfcf | Reagent
| 1 || 2 || 3 || 4
|-
| Vector || 1.4 || 1.4 || 1.3 || 1.3
|-
| Ins 1 || 0.7 || --- || 0.8 || ---
|-
| Ins 2 || 2.9 || --- || 2.9 || ---
|-
| dH<sub>2</sub>O || --- || 3.6 || --- || 3.7
|-
| &nbsp; || 5.0 μL || 5.0 μL || 5.0 μL || 5.0 μL
|}
* Add each to one aliquot of 15.0 Gibson mix (Rene); total = 20.0 μL
* Thermal cycler: 50°C,60 min.; 4°C, ∞
'''Transformation'''
* (1) Transform: add '''2.0 μL''' to 40 μL DH5α-Turbo; ice/5 min.; plate on warm 100 μg/mL amp. agar
* (2) NEB also suggests diluting 5.0 μL of the Gibson reaction into 15.0 μL dH<sub>2</sub>O (20.0 total vol.), and using 2.0 μL diluted DNA, [http://www.neb.com/nebecomm/products/protocol820.asp]
* Test both methods (8 plates total)
** Plates 1-4, method 1
** Plates 5-8, method 2




Line 56: Line 129:
# hPCD + BL01 + pSB1A3
# hPCD + BL01 + pSB1A3


* Check the sequences for BsmBI sites!
 
* Check the sequences for BsmBI docking sites (CGTCTC)
** hPCD - none
** BL01: hPCD-mCherry-SP1AB - none
** V0120 - <font color="red">5 sites</font>
** pSB1A3 - none
 


'''PCR'''
'''PCR'''
# V0120, gg_BBS F / gg_BBP R
# V0120, gg_BBS F (gg0001) / gg_BBP R (gg0002)
# pSB1A3, gg_BBS F / gg_BBP R
# pSB1A3, gg_BBS F (gg0001) / gg_BBP R (gg0002)
# hPCD, gg_BBP-hPCD F / gg_hPCD-BL01 R
# hPCD, gg_BBP-hPCD F (gg0003) / gg_hPCD-BL01 R (gg0004)
# BL01, gg_BL01 F / gg_BL01-BBS R
# BL01, gg_BL01 F (gg0004) / gg_BL01-BBS R (gg0005)


{| {{table}} border="1" cellspacing="3" <!-- Digest check rxn. table -->
{| {{table}} border="1" cellspacing="3" <!-- Digest check rxn. table -->
Line 68: Line 147:
| bgcolor=#cfcfcf | Reagent
| bgcolor=#cfcfcf | Reagent
| bgcolor=#cfcfcf | Volume  
| bgcolor=#cfcfcf | Volume  
| rowspan="7" | <u>Expected:</u><br>1. V0120 = size<br>2. pSB1A3 = size<br>3. hPCD = size<br>4. BL01 = size
| rowspan="7" | <u>Expected:</u><br>gg1. V0120 = 3200<br>gg2. pSB1A3 = 2000<br>gg3. hPCD = 186<br>gg4. BL01 = 2520
| rowspan="7" | <!-- [[Image:GelImage.jpg|400px|Hover name]]<br>15 μL/lane; 1% agarose; [http://openwetware.org/wiki/Image:KAH_Fermentas_GeneRuler_1kbplus.jpg Ladder] -->
| rowspan="7" | [[Image:KAH010513_gel1.jpg|300px|PCR gel]]<br>10 μL/lane; 1% agarose; [http://openwetware.org/wiki/Image:KAH_Fermentas_GeneRuler_1kbplus.jpg Ladder]
|-
|-
| DNA(plasmid) || 0.5 μL
| DNA(plasmid) || 0.5 μL
Line 79: Line 158:
| 2x GoTaq mix || 25.0
| 2x GoTaq mix || 25.0
|-
|-
| dH<sub>2</sub>O || ##
| dH<sub>2</sub>O || 22.5
|-
|-
| &nbsp; || 50 μL  
| &nbsp; || 50 μL  
Line 88: Line 167:
* 72°C, 3 min.
* 72°C, 3 min.
* 4°C, ∞
* 4°C, ∞
'''Purification'''
* Cleaned remaining 40 μL of PCR using the Zymo DNA Clean & Concentrator kit
* Eluted samples with 20 μL dH<sub>2</sub>O
'''DNA Concentrations'''
{| {{table}} border="1" cellspacing="3" <!-- Digest check rxn. table -->
|- valign="top"
| bgcolor=#cfcfcf | Sample
| bgcolor=#cfcfcf | OD 260
| bgcolor=#cfcfcf | 260/ 280
| bgcolor=#cfcfcf | ng/μL
|-
| gg1 V0120 || 0.099 || 1.834 || 98.549
|-
| gg2 pSB1A3 || 0.068 || 1.758 || 67.725
|-
| gg3 hPCD || 0.022 || 1.72 || 22.485
|-
| gg4 BL01 || 0.056 || 1.707 || 55.883
|}




Latest revision as of 22:20, 26 September 2017

Karmella's BioBrick Cloning Main project page
Previous entry      Next entry

01/05/13

  • Gibson: PCR parts, complete protocol for Brady's construct
  • Golden gate: PCR parts; waiting on BsmBI from NEB


Gibson Assembly

  1. hPCD + BL01 + V0120
  2. hPCD + BL01 + pSB1A3


PCR

  1. V0120, Gib_BBS F (Gib0001) / Gib_BBP R (Gib0002)
  2. pSB1A3, Gib_BBS F (Gib0001) / Gib_BBP R (Gib0002)
  3. hPCD, BBP-hPCD fwd (BL9) / hPCD-BL01 rev (BL7)
  4. BL01, hPCD-BL01 fwd (BL8) / BL01-BBS rev (BL10)
Reagent Volume Expected:
G1. V0120 = 3200
G2. pSB1A3 = 2000
G3. hPCD = 186
G4. BL01 = 2520 		PCR gel
10 μL/lane; 1% agarose; Ladder
DNA(plasmid) 0.5 μL
10 μM primer 1 1.0
10 μM primer 2 1.0
2x GoTaq mix 25.0
dH2O 22.5
  50 μL
  • 95°C, 3 min.
  • [95°C, 30 sec.; 57°C, 30 sec.; 72°C, 2 min.] x 30
  • 72°C, 3 min.
  • 4°C, ∞


Purification

  • Cleaned remaining 40 μL of PCR using the Zymo DNA Clean & Concentrator kit
  • Eluted samples with 20 μL dH2O


DNA Concentrations

Sample OD 260 260/ 280 ng/μL
G1 V0120 0.108 1.801 108.375
G2 pSB1A3 0.101 1.849 100.553
G3 hPCD 0.034 1.876 33.586
G4 BL01 0.113 1.828 112.79


Reaction set-up

  • Use 0.2 - 0.5 pmol, per NEB's suggestion, [1]
  • pmols = ng x 1000 / bp x 650 daltons; ng = (pmols x bp x 650 daltons) / 1000
  • Total volume of DNA = 5.0 μL max

1. hPCD + BL01 + V0120

  • vector V0120, 0.1 pmol = 208 ng = 1.9 μL (use 1.4 μL)
  • 2:1 insert hPCD, 0.2 pmol = 24 ng = 0.7 μL
  • 2:1 insert BL01, 0.2 pmol = 328 ng = 2.9 μL

2. hPCD + BL01 + V0120

  • vector pSB1A3, 0.1 pmol = 130 ng = 1.3 μL
  • 2:1 insert hPCD, 0.2 pmol = 24 ng = 0.7 μL (use 0.8 μL)
  • 2:1 insert BL01, 0.2 pmol = 328 ng = 2.9 μL


Gibson reactions:

  1. hPCD + BL01 + V0120
  2. V0120
  3. hPCD + BL01 + pSB1A3
  4. pSB1A3
Reagent 1 2 3 4
Vector 1.4 1.4 1.3 1.3
Ins 1 0.7 --- 0.8 ---
Ins 2 2.9 --- 2.9 ---
dH2O --- 3.6 --- 3.7
  5.0 μL 5.0 μL 5.0 μL 5.0 μL
  • Add each to one aliquot of 15.0 Gibson mix (Rene); total = 20.0 μL
  • Thermal cycler: 50°C,60 min.; 4°C, ∞


Transformation

  • (1) Transform: add 2.0 μL to 40 μL DH5α-Turbo; ice/5 min.; plate on warm 100 μg/mL amp. agar
  • (2) NEB also suggests diluting 5.0 μL of the Gibson reaction into 15.0 μL dH2O (20.0 total vol.), and using 2.0 μL diluted DNA, [2]
  • Test both methods (8 plates total)
    • Plates 1-4, method 1
    • Plates 5-8, method 2


Golden Gate Assembly

  • Try new protocol from Dave Savage
  1. hPCD + BL01 + V0120
  2. hPCD + BL01 + pSB1A3


  • Check the sequences for BsmBI docking sites (CGTCTC)
    • hPCD - none
    • BL01: hPCD-mCherry-SP1AB - none
    • V0120 - 5 sites
    • pSB1A3 - none


PCR

  1. V0120, gg_BBS F (gg0001) / gg_BBP R (gg0002)
  2. pSB1A3, gg_BBS F (gg0001) / gg_BBP R (gg0002)
  3. hPCD, gg_BBP-hPCD F (gg0003) / gg_hPCD-BL01 R (gg0004)
  4. BL01, gg_BL01 F (gg0004) / gg_BL01-BBS R (gg0005)
Reagent Volume Expected:
gg1. V0120 = 3200
gg2. pSB1A3 = 2000
gg3. hPCD = 186
gg4. BL01 = 2520 		PCR gel
10 μL/lane; 1% agarose; Ladder
DNA(plasmid) 0.5 μL
10 μM primer 1 1.0
10 μM primer 2 1.0
2x GoTaq mix 25.0
dH2O 22.5
  50 μL
  • 95°C, 3 min.
  • [95°C, 30 sec.; 57°C, 30 sec.; 72°C, 2 min.] x 30
  • 72°C, 3 min.
  • 4°C, ∞


Purification

  • Cleaned remaining 40 μL of PCR using the Zymo DNA Clean & Concentrator kit
  • Eluted samples with 20 μL dH2O


DNA Concentrations

Sample OD 260 260/ 280 ng/μL
gg1 V0120 0.099 1.834 98.549
gg2 pSB1A3 0.068 1.758 67.725
gg3 hPCD 0.022 1.72 22.485
gg4 BL01 0.056 1.707 55.883




Retrieved from "https://openwetware.org/mediawiki/index.php?title=User:Karmella_Haynes/Notebook/BioBrick_cloning/2013/01/05&oldid=1011724"