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        FOOTPRINTING WITH DNASE1

        互联网

        1606

        1)probe: same as used for gelshift), isolated by isotacelectrophoresis w/out EtOH ppt which can enature dsDNA

        2)probe mix/rxn: volumes x # samples

        1μl probe (0.1©0.5ng or 10©20kcpm)
          0.15μl 20mM EDTA
          0.4μl 10μg/μl dIdC or dAdT (from gel shift assay)
          0.5μl H2O

        3)DNAse mix: made up near end of binding incubations. DNAse l(Worthington DPFF,Cat#LS0006330, lot #58A047,5mg) is 1mg/ml in150mM NaCl, 50% glycerol, store at ©20℃.

        Try 3 different [s] ofDNAse mix (A,B,C)
          1,2 & 3μl stock DNAse1
          2 μl 1M MgCl2
          ©> 100μl H2O

        4)binding rxn: components titrated & optimized by gel shiftassays

        2μl probe mix
          Xμl extract
          ©>18μl NEB (see nucprp.ptc)
          30' RT

        5)DNAse rxn: add 2μl DNAse mix to binding rxn

        inc 1' RT
          stop w/ 100μl DNAse stop mix:

                            stock/50ml
        6M Urea         18g
        0.4M NaCl            6.6ml  3M
        1% SDS              5ml   10%
        20mM EDTA            4ml   250mM
        10mM Tris 8          0.5ml  1M
        0.8M NH4OAc          5ml   8M
        10μg/ml glycogen     50μl  10mg/ml

        5)P/CHCl3 ext

        6)EtOH ppt

        7)PAGE: Resuspend carefully in 8μl sequencing sample buffer (5'vortex, 5' 60℃, 1' vortex, 2' 90℃, spin, transfer to new tube,count cpm). Load equal counts on 6% or gradient sequencing gel.

        Notes: If extract inhibits DNAse, add 0.1©0.3μl extra DNAse mixto binding rxns.

        DNAse requires Mg, some factors are inactivatedby it! Remember μg/KB x 0.66 = picomole thus 1ng of 300bp probe =2 femptomole.

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