Daniel:Notebook/ComboLock/2016-9-28: Difference between revisions

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>Djacobse
>Djacobse
 
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| align="center" align="center" |  
| align="center" align="center" |  
|style="font-weight:bold" align="center" align="center" | 50
|style="font-weight:bold" align="center" align="center" | 50
|}
<li>Add amplicons according to following table</li>
{| class="wikitable" <hiddentext>generated with [[:de:Wikipedia:Helferlein/VBA-Macro for EXCEL tableconversion]] V1.8</hiddentext>
|- style="background-color:#CCC0DA;font-size:12pt;font-weight:bold" align="center"
| width="65" height="45" | Sample
| width="65" | PCAmp1
| width="65" | PCAmp3
| width="65" | LatchX2
| width="65" | LatchX3
|- style="font-size:12pt"
| height="15" align="center" | AmpliconX1
| align="center" | X
| align="center"  valign="bottom" | &nbsp;
| align="center" valign="bottom" | X
| align="center"  valign="bottom" | &nbsp;
|- style="background-color:#D9D9D9;font-size:12pt" align="center"
| height="15" | AmpliconX3
| align="center" | &nbsp;
| X
| align="center" | &nbsp;
| X


|}
|}
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|- style="font-size:12pt"
|- style="font-size:12pt"
| height="15"  valign="bottom" | C4-C2 Amplicon
| height="15"  valign="bottom" | C4-C2 Amplicon
| align="center" align="center" valign="bottom" | &nbsp;
| align="center" align="center" valign="bottom" | 557.1


|}
|}
==Protocol (Part 2)==
<ol start="4">
<li>Size Select</li>
<ol type="A">
<li>For sample lanes, mix 32 uL sample, 28 uL 6X loading dye and 100 uL TBE (160 uL total)</li>
<li>For ladder lanes, mix 4 uL 25bp ladder, 6 uL 6X loading dye and 30 uL TBE (40 uL total)</li>
<li>Add 20 uL to each lane (2 gels total, 1 per sample)</li>
<li>Run gel for 25 minutes at 250V</li>
<li>While running, prepare tubes by puncturing a 0.5 mL tube with a 0.22 gauge needle and putting inside a 1.5 mL tube</li>
<li>Stain gel for 3 minutes with 3 uL SYBR gold</li>
<li>Image in gel doc</li>
<li>Extract bands at 104 bp and put into tubes; 2 lanes per tube (4 tubes total, 2 per sample)</li>
<li>Image in gel doc post-extraction</li>
<gallery perrow=2 heights=300px widths=300px>
File:2016-09-28-PCAmp4Prod-SizeSelect.png|Before Image
File:2016-09-28-PCAmp4Prod-SizeSelect-After.png|After Image
</gallery>
<li>Centrifuge tubes at 12000rpm for 1.5 minutes</li>
<li>Discard 0.5 mL tube and resuspend in 500 uL TE buffer</li>
<li>Incubate at 37C overnight with vigorous shaking; continued [[Daniel:Notebook/ComboLock/2016-9-29|tomorrow]]</li>
</ol></ol>
[[Category:ComboLock]] [[Category:20160928]]

Latest revision as of 17:31, 29 September 2016

Positive Control Amplicon Production (PCAmp4)[edit]

Back to Calendar

Protocol[edit]

  1. Phosphorylation
    1. In a 0.2 mL tube, add ingredients according to table
    2. Reagent Stock Conc Final Conc./Amount uL added
      AmpLigase Reaction Buffer 10X 1X 2
      ATP 10 mM 1 mM 2
      PCAmp2 100 uM 1 nmol total 10
      T4 DNA Kinase 10 U/uL 10 U 1
      nfH2O NA NA 5
      Total     20
    3. Incubate at 37C for 30 min
  2. Ligation
    1. Set up 2 reactions with the following reagents (DO NOT ADD LIGASE YET)
    2. Reagent Stock Conc Final Conc./Amount uL added
      AmpLigase Reaction Buffer 10X 1X 4
      Latch Oligo 100 uM 500 umol 5
      5' Amplicon Oligo 100 uM 500 umol 5
      Amp Ligase 5 U/uL 5 U 1
      Phosphate Reaction NA NA 10
      nfH2O NA NA 25
      Total     50
    3. Heat reaction to 95C for 5 min
    4. Lower temp to 55C
    5. Add 1 uL Amp Ligase to each reaction without removing from thermocycler; swirl with pipette tip 5 times to mix
    6. Incubate at 55C for 2 hours
    7. Heat to 95 C to denature dsDNA
    8. Purify with ssDNA column
  3. ssDNA Column
    1. Add 100 uL Binding Buffer to the sample; mix well
    2. Transfer to IIC Column and centrifuge at 14000 rpm for 1 minute; SAVE THE FLOW THROUGH
    3. Add 150 uL 100% EtOH to flow through; mix well
    4. Transfer to IC Column and centrifuge at 14000 rpm for 1 minute; discard flow through
    5. Add 400 uL Prep Buffer and centrifuge at 14000 rpm for 1 minute; discard flow through
    6. Add 700 uL Wash Buffer and centrifuge at 14000 rpm for 1 minute; discard flow through
    7. Add 400 uL Wash Buffer and centrifuge at 14000 rpm for 1 minute; discard flow through
    8. Centrifuge empty column at 14000 rpm for 2 minutes
    9. Transfer to empty 1.5mL centrifuge tube (low bind)
    10. Add 30 uL nfH2O and centrifuge at 14000 rpm for 1 minute

    Nanodrop Results[edit]

    Sample ng/uL ssDNA
    C4-C2 Amplicon 557.1

    Protocol (Part 2)[edit]

    1. Size Select
      1. For sample lanes, mix 32 uL sample, 28 uL 6X loading dye and 100 uL TBE (160 uL total)
      2. For ladder lanes, mix 4 uL 25bp ladder, 6 uL 6X loading dye and 30 uL TBE (40 uL total)
      3. Add 20 uL to each lane (2 gels total, 1 per sample)
      4. Run gel for 25 minutes at 250V
      5. While running, prepare tubes by puncturing a 0.5 mL tube with a 0.22 gauge needle and putting inside a 1.5 mL tube
      6. Stain gel for 3 minutes with 3 uL SYBR gold
      7. Image in gel doc
      8. Extract bands at 104 bp and put into tubes; 2 lanes per tube (4 tubes total, 2 per sample)
      9. Image in gel doc post-extraction
      10. Centrifuge tubes at 12000rpm for 1.5 minutes
      11. Discard 0.5 mL tube and resuspend in 500 uL TE buffer
      12. Incubate at 37C overnight with vigorous shaking; continued tomorrow