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文献和实验【精华】vol 687 Chapter 3 采用Splinkerette-PCR技术对前病毒基因组插入位点进行分离
of methods used to uncover insertion sites have previouslybeen described, including genomic DNA library screening(15), ligation-mediated PCR (6), inverse PCR (16), VISAtechnique (17), T-linker PCR (18), and single nucleotidepolymorphism-based mapping (19
Combined 3C-ChIP-Cloning (6C) Assay: A Tool to Unravel Protein-Mediated Genome Architecture
analysis. Restriction enzyme buffer (10X) Dilute the 10X stock to 1.14X for Steps 12 and 13. RNase A, DNase-free (10 mg/mL; Sigma R6513) SDS (Sodium dodecyl sulfate; 20% w/v; Fisher BP166) Sodium acetate (3 M, pH 5.2
. 2 ml 1 M KCl 1 ml 1 M Tris-HCl, pH 7.6 1 ml 1 M MgCl2 0.1 ml 1 M DTT ddH2 O to 10 ml RNase T1 : 100 U/ul in 50 mM Tris-HCl, pH 7.6 100 μl RNase T1 (Sigma R-8251) (100,000 U/0.2 ml) 25 μl 1 M Tris-HCl, pH 7.6 375 μl ddH2 O 500 μl 10
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