Human Tau (4R isoforms) ELISA Kit is a single-wash 90-min Simplestep used to quantify Human Tau (4R isoforms) with a sensitivity of 3.128 pg/ml. The assay uses a simple mix-wash-read protocol with just one incubation and one wash step.
- Colorimetric Sandwich ELISA - 450 nm readout : works on any standard plate reader
- Design your own immunoassay: we also offer the conjugation-ready antibody pair
Application | Reactivity | Dilution info | Notes |
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Application sELISA | Reactivity Reacts | Dilution info - | Notes - |
Promotes microtubule assembly and stability, and might be involved in the establishment and maintenance of neuronal polarity (PubMed:21985311). The C-terminus binds axonal microtubules while the N-terminus binds neural plasma membrane components, suggesting that tau functions as a linker protein between both (PubMed:21985311, PubMed:32961270). Axonal polarity is predetermined by TAU/MAPT localization (in the neuronal cell) in the domain of the cell body defined by the centrosome. The short isoforms allow plasticity of the cytoskeleton whereas the longer isoforms may preferentially play a role in its stabilization.
MAPT, MAPT
MAPTL, MTBT1, TAU, MAPT, Microtubule-associated protein tau, Neurofibrillary tangle protein, Paired helical filament-tau, PHF-tau
Human Tau (4R isoforms) ELISA Kit is a single-wash 90-min Simplestep used to quantify Human Tau (4R isoforms) with a sensitivity of 3.128 pg/ml. The assay uses a simple mix-wash-read protocol with just one incubation and one wash step.
- Colorimetric Sandwich ELISA - 450 nm readout : works on any standard plate reader
- Design your own immunoassay: we also offer the conjugation-ready antibody pair
Sample | n | mean | SD | C.V. |
---|---|---|---|---|
Sample Extract | n 8 | mean - | SD - | C.V. 5.5 |
Sample | n | mean | SD | C.V. |
---|---|---|---|---|
Sample Extract | n 3 | mean - | SD - | C.V. 5.1 |
Sample type | Average % | Range |
---|---|---|
Sample type Cell culture extracts | Average % = 117 | Range 109 - 123 % |
Sample type Tissue Extracts | Average % = 111 | Range 106 - 119 % |
Human Tau (4R isoforms) SimpleStep ELISA® kit (ab303750) is a single-wash 90 min sandwich ELISA designed for the quantitative measurement of Human Tau (4R isoforms) protein in cell extract and tissue extracts. Quantitate Human Tau (4R isoforms) with 3.128 pg/ml sensitivity.
SimpleStep ELISA® technology employs capture antibodies conjugated to an affinity tag that is recognized by the monoclonal antibody used to coat our SimpleStep ELISA® plates. This approach to sandwich ELISA allows the formation of the antibody-analyte sandwich complex in a single step, significantly reducing assay time. See the SimpleStep ELISA® protocol summary in the image section for further details. Our SimpleStep ELISA® technology provides several benefits:
-Single-wash protocol reduces assay time to 90 minutes or less
-High sensitivity, specificity and reproducibility from superior antibodies
-Fully validated in biological samples
-96-wells plate breakable into 12 x 8 wells strips
A 384-well SimpleStep ELISA® microplate (Pre-coated 384 well Microplate SimpleStep ELISA® ab203359) is available to use as an alternative to the 96-well microplate provided with SimpleStep ELISA® kits.
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Tau also known as microtubule-associated protein Tau (MAPT) plays an important role in stabilizing microtubules in neuronal cells. Tau is primarily found in the central nervous system but also exists in peripheral neurons. Human Tau protein comes in six isoforms due to alternative splicing with molecular weights ranging from 48 kDa to 67 kDa. This protein predominantly locates in the axons of neurons where it maintains the stability of microtubule tracks necessary for axonal transport.
Tau is involved in the assembly and stabilization of microtubules essential for maintaining neuronal structure. It interacts with microtubule-binding domains (MBD) to bind and bundle microtubules facilitating intracellular transport. Tau forms a part of the neuronal cytoskeleton complex working closely with other cytoskeletal proteins to preserve the proper axonal transport and function. Abnormally phosphorylated Tau often termed phospho-Tau disrupts this complex affecting microtubule stability.
Tau has critical involvement in several signaling cascades such as the microtubule-binding and transport pathways. Glycogen synthase kinase 3 beta (GSK3β) and cyclin-dependent kinase 5 (CDK5) frequently phosphorylate Tau controlling its interaction with microtubules. Phosphorylated Tau accumulates leading to the formation of neurofibrillary tangles often observed in neurodegenerative conditions. Additionally Tau interacts with GAPDH impacting cellular energy regulation through potential pathway cross-talk involving oxidative stress responses.
Tau is closely associated with Alzheimer's disease and frontotemporal dementia. In Alzheimer's disease hyperphosphorylated Tau aggregates into paired helical filaments forming neurofibrillary tangles while similar aggregates are observed in frontotemporal dementia. In these conditions Tau links to amyloid precursor protein (APP) where misregulated phosphorylation-driven interactions contribute to neurodegeneration. Identifying phospho-Tau and its altered interactions with related proteins aids in understanding and potentially treating these disorders.
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Example of Human Tau (4R isoforms) standard curve in 1X Cell Extraction Buffer PTR.
Example of Human Tau (4R isoforms) standard curve. Background-subtracted data values (mean +/- SD) are graphed.
Interpolated concentrations of Tau (4R isoforms) in mouse and rat brain tissue extracts.
The concentration of Tau (4R isoforms) was measured in 1.0 – 0.125 mg/mL of mouse brain tissue extracts and in 1.25 – 0.31 mg/mL of rat brain tissue extracts in duplicates. The interpolated dilution factor corrected values are plotted in pg of Tau per μg of extract (mean +/- SD). Sample dilutions are made in 1X Cell Extraction Buffer PTR.
Interpolated concentrations of Human Tau (4R isoforms) in brain tissue (cortex) extract, brain tissue (stem) extract, and SH-SY5Y cell extract.
Interpolated concentration of native Tau (4R isoforms) was measured in duplicate at different sample concentrations. Undiluted samples are as follows: Human brain tissue (cortex) extract 2 μg/mL, Human brain tissue (stem) extract 10 μg/mL, and SH-SY5Y cell extract 15 μg/mL. The interpolated dilution factor corrected values are plotted (mean +/- SD, n=2). Sample dilutions are made in 1X Cell Extraction Buffer PTR.
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