Daniel:Notebook/PosSequencing/2017-7-14: Difference between revisions

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<gallery perrow=2 heights=300px widths=300px mode=packed-hover caption="10 pM template Concentration">
<gallery perrow=2 heights=300px widths=300px mode=packed-hover caption="10 pM template Concentration">
File:
File:EmPCR9-20170714.lif_10pM-Field1-SNAP_ch00.jpg|Field 1
File:
File:EmPCR9-20170714.lif_10pM-Field3-SNAP_ch00.jpg|Field 3
File:
File:EmPCR9-20170714.lif_10pM-Field7-SNAP_ch00.jpg|Field 7
File:
File:EmPCR9-20170714.lif_10pM-Field9-SNAP_ch00.jpg|Field 9
</gallery>
</gallery>


[[Category:PosSeq]] [[Category:20170712]]
[[Category:PosSeq]] [[Category:20170712]]

Latest revision as of 22:40, 14 July 2017

emPCR 9-Concentration Comparison (Started Wednesday)[edit]

Back to Calendar

Protocol-Part 3[edit]

  1. Dye hybridization
    1. Resuspend beads in 30 uL 2X SSC
    2. Mix 15 uL 4X SSC, 9 uL nfH2O, 3 uL 10 uM dcprobe6-A488, and 3 uL 10 uM dcprobe6-Cy5
    3. Incubate master mix in the dark at 80C for 5 minutes
    4. Add 10 uL master mix to each sample
    5. Incubate at 55C for 30 minutes in the dark
    6. Magnet pull down, remove supernatant and add 40 uL 2X SSC buffer
    7. Add 15 uL to a slide for analysis
    8. Seal coverslip with nail polish and wait approximately 30 minutes to dry

Results[edit]