User:Karmella Haynes/Notebook/BioBrick cloning/2013/01/05

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Line 48: Line 48:
* 72°C, 3 min.
* 72°C, 3 min.
* 4°C, ∞
* 4°C, ∞
 +
 +
'''Measure DNA Concentrations'''
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{| {{table}} border="1" cellspacing="3" <!-- Digest check rxn. table -->
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|- valign="top"
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| bgcolor=#cfcfcf | OD 260
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| bgcolor=#cfcfcf | 260/ 280
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| bgcolor=#cfcfcf | ng/μL
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|-
 +
| G1 V0120 || 0.108 || 1.801 || 108.375
 +
|-
 +
| G2 pSB1A3 || 0.101 || 1.849 || 100.553
 +
|-
 +
| G3 hPCD || 0.034 || 1.876 || 33.586
 +
|-
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| G4 BL01 || 0.113 || 1.828 || 112.79
 +
|}
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Line 88: Line 105:
* 72°C, 3 min.
* 72°C, 3 min.
* 4°C, ∞
* 4°C, ∞
 +
 +
 +
'''Measure DNA Concentrations'''
 +
{| {{table}} border="1" cellspacing="3" <!-- Digest check rxn. table -->
 +
|- valign="top"
 +
| 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
 +
|}
 +

Revision as of 18:37, 5 January 2013

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

01/05/13

  • Golden gate: PCR parts, complete protocol for Brady's construct
  • Gibson: PCR parts, complete protocol for Brady's construct



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:
1. V0120 = 3200
2. pSB1A3 = 2000
3. hPCD = 186
4. BL01 = 2520
Image:GelImage.jpg
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, ∞

Measure DNA Concentrations

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



Golden Gate Assembly

  • Try new protocol from Dave Savage
  1. hPCD + BL01 + V0120
  2. hPCD + BL01 + pSB1A3
  • Check the sequences for BsmBI sites!

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:
1. V0120 = 3200
2. pSB1A3 = 2000
3. hPCD = 186
4. BL01 = 2520
Image:GelImage.jpg
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, ∞


Measure DNA Concentrations

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




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