Rabbit Recombinant Monoclonal TAU phospho T217 antibody. Carrier free. Suitable for I-ELISA, ICC/IF, WB and reacts with Human, Rat samples. Immunogen corresponding to Synthetic Peptide within Human TAU_HUMAN phospho T217.
IgG
Rabbit
pH: 7.4
Constituents: 100% PBS
Liquid
Monoclonal
I-ELISA | ICC/IF | WB | |
---|---|---|---|
Human | Tested | Expected | Tested |
Rat | Expected | Tested | Expected |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 1 µg/mL | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Rat | Dilution info Use at an assay dependent concentration. | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Rat | Dilution info 1/250 | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info Use at an assay dependent concentration. | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 1/1000 | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Rat | Dilution info Use at an assay dependent concentration. | 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.
Microtubule-associated protein tau, Neurofibrillary tangle protein, Paired helical filament-tau, PHF-tau, TAU, MTBT1, MAPT, MAPTL
Rabbit Recombinant Monoclonal TAU phospho T217 antibody. Carrier free. Suitable for I-ELISA, ICC/IF, WB and reacts with Human, Rat samples. Immunogen corresponding to Synthetic Peptide within Human TAU_HUMAN phospho T217.
IgG
Rabbit
pH: 7.4
Constituents: 100% PBS
Liquid
Monoclonal
Yes
HL1276
Affinity purification Protein A
Blue Ice
1-2 weeks
+4°C
+4°C
Upon delivery aliquot
Avoid freeze / thaw cycle
This product is a recombinant monoclonal antibody, which offers several advantages including:
For more information, read more on recombinant antibodies.
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. The carrier-free buffer and high concentration allow for increased conjugation efficiency.
This conjugation-ready format is designed for use with fluorochromes, metal isotopes, oligonucleotides, and enzymes, which makes them ideal for antibody labelling, functional and cell-based assays, flow-based assays (e.g. mass cytometry) and Multiplex Imaging applications.
Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with 1 minute hands-on-time and 100% antibody recovery: available for fluorescent dyes, HRP, biotin and gold.
This supplementary information is collated from multiple sources and compiled automatically.
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.
We have tested this species and application combination and it works. It is covered by our product promise.
We have not tested this specific species and application combination in-house, but expect it will work. It is covered by our product promise.
This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
We do not recommend this combination. It is not covered by our product promise.
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All lanes: Western blot - Anti-Tau (phospho T217) antibody [HL1276] (ab308355) at 1/1000 dilution
Lane 1: Untreated (–) SK-N-SH whole cell extract at 30 µg
Lane 2: Treated (+) SK-N-SH whole cell extract at 30 µg
All lanes: HRP-conjugated anti-rabbit IgG antibody
Predicted band size: 78 kDa
For immunofluorescence analysis, DIV9 rat E18 primary cortical neuron cells were fixed in 4% paraformaldehyde at room temperature for 15 minutes and permeabilized for detection of Tau (phospho T217) protein using ab308355 at 1/250 dilution (green). Nuclei (blue) is stained with fluoroshield with DAPI. Tau, an axon marker counterstain (red) diluted at 1/500
For immunofluorescence analysis, DIV10 rat E18 primary hippocampal neuron cells were fixed in 4% paraformaldehyde at room temperature for 15 minutes and permeabilized for detection of Tau (phospho T217) protein using ab308355 at 1/250 dilution (green). Nuclei (blue) is stained with fluoroshield with DAPI. Tau, an axon marker counterstain (red) diluted at 1/500
Indirect ELISA analysis was performed by coating the plate with Tau peptide and Tau (phospho T217) peptide (1000-15.63 ng/mL). Coated peptides were probed with Tau (phospho T217) antibody [HL1276] (ab308355) (1 μg/mL). Goat anti-rabbit IgG antibody (HRP) (1/10000) was used to detect the bound primary antibody.
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