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文献和实验medium (MCDB-131 medium with 5 ml of 200 mM L-glutamine, 10% FBS and EGM-2 SingleQuots) at 37 °C, 5% CO2 . 5) Slowly change medium every 24 hours for the first 7 days, then every other day. EPC colonies can be identified after an average
Combined 3C-ChIP-Cloning (6C) Assay: A Tool to Unravel Protein-Mediated Genome Architecture
; Fisher BP333) T4 DNA ligase (400 U/µL) TE buffer (pH 8.0) Dilute 10X stock to 1X before use. Triton X-100 (20% v/v; VWR) Trypsin (1X; Invitrogen 25300) Equipment Aluminum foil Cell scraper Centrifuge
. 6. 10× Tango buffer (Thermo Scientifi c/Fermentas). 7. DTT (DL-Dithiothreitol; Cleland’s reagent). 8. 10 mM Adenosine 5′-triphosphate. 9. Ultrapure water (RNAse/DNAse-free). 10. Tris-EDTA (TE) buffer. 11. E. coli competent cells. Strains
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