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Water molecules were cleaned off from the protein crystal structure before docking.
These DNA molecules were cleaned up with Qiagen's QIAquick PCR Purification Kit.
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For single molecule imaging, cover slips were cleaned with a plasma cleaner (Solaris Model 950, Gatan) with an H2/O2mixture for 2 min, then coated with poly-L-lysine.
The target and substrates were cleaned by a neutral molecule source (NMS).
Pens were cleaned weekly.
Data were cleaned.
were cleaned before each assay.
There are no significant differences between FTIR spectra in Figure 2d, c due to the presence of extra DEG molecules; after the coated Gd2O3 was cleaned up by dialysis and centrifuge, unreacted DEG has been removed.
Before docking, the protein crystal structure was cleaned by removing the water molecules.
RNA was cleaned with RNA Clean-up kit (Macherey-Nagel).
Excess adaptor molecules were removed by reaction clean-up (QIAquick PCR Purification Kit, QIAGEN, Valencia CA), followed by preparative gel electrophoresis (1.5 V/cm, 18 h) on a 1% SeaKem GTG Agarose gel in 1X TAE buffer (gel size = 23 cm width ×40 cm length, gel volume = 600 ml, well size = 7.2 mm width, 1.5 mm thickness).
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