Matt:LabNotes/2016-4-11

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Revision as of 00:39, 13 April 2016 by >Mzcai
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  1. Wash with nf-H2O twice
  2. Prepare Ampligase mix on ice
    • Preheat H2O + Padlock probes to 85C and then snap cool before adding Ampligase buffer and enzyme
  • Combine B11 and B12: 100ul at ~200nM
    • B12 looked to have some very fine PA gel still in there (not filtered enough?)
Component Volume
DEPC-H2O 47
Ampligase Buffer 10
Batch 11 & 12 Padlock Probes ~200nM]] 33
Ampligase 10
Total 100
  1. Add mix to sample and incubate for 30min at 37C
  2. Move sample to 60C and oven slowly decreases to 55C and held for ~24hr

Day 2

  1. Wash with 1X PBS once
  2. Add 1uM FISSEQ_ppRCA (1ul 200uM FISSEQ_ppRCA + 199ul 2X SSC + 30% formamide) and incubate 1hr at 55C
    • Preheated to 70C before adding
  3. Wash with 2X SSC once, 1X SSC once, and 1X PBS once
  4. Add RCA mix and incubate 15hr at 30C
Component Volume
H2O 174
10X Phi29 Buffer 20
25mM dNTP 2
4mM aa-dUTP 2
Phi 29 (low conc) 2
Total 200