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Tau 2.0 kit

Manufactured by Quanterix

The Tau 2.0 kit is a lab equipment product from Quanterix. It is designed for the quantitative measurement of tau protein, a biomarker associated with various neurological conditions. The kit provides the necessary reagents and materials for performing this analysis.

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3 protocols using tau 2.0 kit

1

Quantification of Plasma Neurodegeneration Biomarkers

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Non-fasting blood samples were collected for all participants. Blood was
collected into plastic dipotassium ethylene diaminetetraacetic acid tubes, and
processed according to standard procedures, with plasma aliquoted and frozen at
−80°C. Frozen plasma aliquots were shipped on dry ice to the
University of Gothenburg (Sweden) for batch analysis. Plasma p-tau181concentration was measured using an in-house single molecule array method on an
HD-X analyzer (Quanterix), as previously described in detail.11 (link) The lower limit of
quantification (LLoQ) was 1.0 pg/mL, with a dynamic range of 1.0 to 128.0 pg/mL.
An in-house Simoa method was used to measure plasma NfL concentration
(Quanterix), as described by Gisslén et al.44 (link) The LLoQ was 1.9 pg/mL, with a dynamic
range of 1.9 to 1800 pg/mL. Plasma T-tau concentration was measured using Tau
2.0 kit and the HD-1 analyzer (Quanterix) with an LLoQ of 0.061 pg/mL and a
dynamic range of 0.061 to 360 pg/mL. The measurements were performed in one
round of experiments, using one batch of reagents. Intra-assay coefficients of
variation were below 10% for all the biomarkers.
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2

Plasma NfL and T-tau Biomarker Measurements

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Non-fasting blood samples were collected for all participants. Blood was collected into plastic dipotassium EDTA tubes, and processed according to standard procedures, with plasma aliquoted and frozen at −80°C. Frozen plasma aliquots were shipped on dry ice to the University of Gothenburg (Sweden) for batch analysis. Plasma NfL concentration was measured using an ultrasensitive in-house Simoa method on an HD-1 Analyzer (Quanterix, Billerica, Massachusetts), as previously described in detail (Gisslen et al., 2016 (link)). This in-house Simoa assay is very similar to commercial Simoa methods (only minor variations) and this same method was previously found to have a high correlation (r = .89) with CSF NfL in a sample of patients with HIV infections (Gisslen et al., 2016 (link)). The LLOQ was 1.9 pg/mL, with a dynamic range of 1.9-1800 pg/mL. T-tau concentrations were measured using the commercially available Tau 2.0 kit and the HD-1 Analyzer (Quanterix, Billerica, Massachusetts) with an LLOQ of 0.061 pg/mL and a dynamic range of 0.061-360 pg/mL. The measurements were performed by board-certified laboratory technicians who were blinded to clinical data. All samples were detectable with an average coefficient of variation (CV) of 4%.
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3

Neurological Biomarker Quantification

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Following blood processing as described above, 0.5 mL plasma aliquots were stored at − 80 °C until shipment on dry ice to the University of Gothenburg for analysis. Plasma NfL and total tau levels were measured using the single molecule array (Simoa) HD-1 Analyzer (Quanterix, Billerica, MA, USA). For T-tau, the commercially available Tau 2.0 kit was used according to the manufacturer’s instructions (Quanterix). For NfL, a previously described in-house Simoa assay was used [44 (link)]. Calibrators were run in duplicate, and obvious outlier calibrator replicates were masked before curve fitting. Samples were run in singlicate with 4-fold dilution. Two quality control samples were run in duplicate at the beginning and end of each run.
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