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Innotest phospho tau 181p kit

Manufactured by Fujirebio
Sourced in Belgium, United States

The Innotest Phospho-Tau(181P) kit is a laboratory assay used to quantitatively determine the concentration of phosphorylated tau protein at threonine 181 (P-tau181) in human cerebrospinal fluid (CSF) samples. The kit utilizes an enzyme-linked immunosorbent assay (ELISA) technique.

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2 protocols using innotest phospho tau 181p kit

1

Quantifying Neurological Biomarkers in Plasma

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Plasma samples were analyzed using the Neurology 4-Plex “A” kit on the Simoa HD-1 analyser (Quanterix, Billerica, MA, USA) at University College London and Mayo Clinic, following manufacturer instructions. The Simoa platform is an ultrasensitive digital ELISA as previously described42 (link). The Neurology 4-Plex “A” kit allows the simultaneous quantification of total tau (t-tau), NfL, GFAP and UCHL143 . For each sample, measurements were performed in duplicates, and average values with a coefficient of variation (CV) below 20% were considered. CSF t-tau and phosphorylated tau181 (p-tau181) were quantified with conventional ELISA using, respectively, the Innotest hTau Ag assay and the Innotest Phospho-Tau(181P) kit (Fujirebio Europe N.V., Gent, Belgium).
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2

Multiplex Biomarker Quantification in CSF

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For AD core biomarkers, we used the V-PLEX Aβ Peptide Panel 1 (6E10) Kit (K15200E) and the V-PLEX Human Total Tau Kit (K151LAE) (Mesoscale Diagnostics LLC, Rockville, MD, USA), as well as the INNOTEST PHOSPHO TAU(181P) kit (81581, Fujirebio, Ghent, Belgium). For inflammation-associated proteins, detailed information is provided in Additional file 1.
In the initial evaluative step, all inflammatory markers were classified as detectable, undetectable, or borderline. The last group contained markers at detection limits for which test results suggested that addition of a known dose of protein to the sample could be used to improve the assay signal (spike-in concept). A full record of this test phase is provided in Additional file 1.
CSF samples saved strictly for research purposes had been snap-frozen in liquid nitrogen and stored in a biobank at −80 °C. Prior to assay, samples were thawed on ice and divided into aliquots (total of two freeze-thaw cycles). All further sample processing was conducted on ice until samples were applied to the assays. Samples and calibrators were run in duplicates, and samples with a coefficient of variation (CV) > 20% were repeated. To normalize for interrun variance, a pooled and aliquoted CSF sample was run as an internal standard on each assay plate.
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