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The PFOS values of all samples were detected, and for samples with PFOA levels below the detection limit (0.50 ng/mL) (n = 17, 5.5% of participants), we used a value of half the detection limit (0.25 ng/mL).
All samples were detected by Western blotting using an anti-His monoclonal antibody.
All samples were detected by DNA sequencing, and the two samples with controversial results were confirmed positive.
In order to distinguish positive and negative results of HBV infection by FP values, all samples were detected for HBV infection by ELISA method.
All samples were detected with the same parameters.
Note: N/A, not available because nearly all samples were detected to deviate significantly from the normal distribution.
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The d-dimer level of all samples was detected with an ACL TOP automatic coagulation analyzer (Beckman Coulter, Inc., AmericaBrea, CA, USA) using latex immunoturbidimetry.
The morphology and structure of all samples are detected by X-ray diffraction (XRD), scanning electron microscopy (SEM), high resolution transmission electron microscopy (HRTEM) and X-ray photoelectron spectroscopy (XPS).
HEV RNA in all samples was detected using a real-time RT-PCR assay targeting ORF3 [ 38].
During purification, all protein samples were detected and analyzed by SDS-PAGE coupled with Coomassie blue staining.
All reverse transcribed samples were detected by all three PCR reactions.
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