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Human Tau OneStep ELISA Kit

Human Tau OneStep ELISA Kit

Catalog Number: S0C3159 Reactivity: Human Conjugation: Brand: Starter
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Regular price $500 USD
Regular price Sale price $500 USD
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Product Details

Product Specification


Antigen Tau
Immunogen Recombinant Protein
Antibody Type Recombinant mAb
Reactivity Hu
Predicted Reactivity Mk
Purification Protein A
Stability & Storage

12 months from date of receipt / reconstitution, 2 to 8°C as supplied.

Kit


Precision Intra-assay: 2.6%;
Inter-assay: 4.2%
Sample type Cell culture supernatant; Serum; EDTA Plasma, Heparin Plasma, Citrate Plasma, Cell culture extracts
Assay type Sandwich (quantitative)
Sensitivity 6.71 pg/mL
Range 31.25 pg/mL – 2000 pg/mL
Recovery Cell culture supernatant: 109%
Serum: 91%
EDTA Plasma: 91%
Heparin Plasma: 88%
Citrate Plasma: 88%
Cell culture extracts: 94%
Assay time 60 minutes
Species reactivity Hu

Background

Human Tau is a microtubule-associated protein predominantly expressed in neurons of the central nervous system, where its primary physiological function is to promote microtubule assembly and stability. Encoded by the MAPT gene, this protein is crucial for axonal transport and neuronal morphology due to its ability to bind and stabilize microtubules. Tau is characterized as an intrinsically disordered protein, exhibiting a high degree of conformational flexibility. Structurally, it features a projection domain at the N-terminus and a microtubule-binding domain at the C-terminus, which contains three or four conserved repeat sequences responsible for its interaction with tubulin. In a healthy neuron, tau dynamically regulates microtubule dynamics, but its normal function is tightly controlled by post-translational modifications, particularly phosphorylation. Hyperphosphorylation of tau is a hallmark pathological event, leading to its detachment from microtubules, which subsequently destabilizes the neuronal cytoskeleton and impairs axonal transport. The detached, hyperphosphorylated tau proteins have a high propensity to misfold and aggregate into paired helical filaments, which further assemble into larger insoluble neurofibrillary tangles. These tangles are one of the defining neuropathological lesions in Alzheimer's disease and a spectrum of other neurodegenerative disorders collectively known as tauopathies.

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ELISA