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Chromatin prepared using the two methods was prepared from cultured CD4+ lymphocytes, and immunoprecipitated with anti-H3K4me3 antibody.
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These four purification methods were prepared by using specific ligands (RAC and RAC-ovalbumin) and commercial ligands (protein G and protein A), respectively.
The perovskite liquid solution used in the anti-solvent and spray methods were prepared by dissolving 158 mg of MAI and 420 mg of PbI2 powders in 1 ml of dimethyl sulfoxide (DMSO).
All antigens used in these methods were prepared from whole adult worms.
Whole-cell cDNA libraries from messenger RNA molecules (Materials and Methods) were prepared in two human cell lines: the myelogenous leukemia cell line K562 and cervical cancer HeLa cells.
Each calibration method was prepared following its own procedure (c.f. Figure 1, panels A and C).
A set of standards to test the linearity of the method was prepared using myoglobin digest and peptide standards.
Prior to sample testing a positive control for the isolation method was prepared from a sample of fresh homogenised faeces previously determined to be negative for the presence of Salmonella by direct and enrichment culturing methods [ 47, 53, 54].
Future validation of these methods is preparing planned on a prospective study.
The samples used the BET method were prepared under the condition of γ = 0.97.
The experimental results of the proposed method are prepared in this section to show the (2, 4 -threshold SIS scheme.
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