“…The phosphate-modified crystals SC-5p and EC-5p were moved into the buffer using a cryoloop (Hampton Research) and washed in buffer (0.030 M sodium dimethyl arsonate, 0.055 M MgCl 2 , 0.050 M NaCl, 0.025 M HEPES (pH = 6)) for 10 min to remove the excess DNA strands. 42 After washing, the crystals were transferred to chemical ligation wells containing an equal mixture of EDC crosslinking agent and buffer. The ligation reaction was left to stand for 24 hours.…”
Porous DNA crystals with high intrinsic biocompatibility were designed to be used as scaffold materials, loaded with fluorescent guest molecules (fluorescent proteins/rare earth complexes) to detect anti-cancer drugs.
“…The phosphate-modified crystals SC-5p and EC-5p were moved into the buffer using a cryoloop (Hampton Research) and washed in buffer (0.030 M sodium dimethyl arsonate, 0.055 M MgCl 2 , 0.050 M NaCl, 0.025 M HEPES (pH = 6)) for 10 min to remove the excess DNA strands. 42 After washing, the crystals were transferred to chemical ligation wells containing an equal mixture of EDC crosslinking agent and buffer. The ligation reaction was left to stand for 24 hours.…”
Porous DNA crystals with high intrinsic biocompatibility were designed to be used as scaffold materials, loaded with fluorescent guest molecules (fluorescent proteins/rare earth complexes) to detect anti-cancer drugs.
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