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Anti-Tau (phospho T181) antibody [EPR23506-107] (ab254409) is a rabbit monoclonal antibody that is used to detect Tau in Western Blot, IP, IHC-P, IHC-Fr, ELISA, Dot Blot. Suitable for Human, Mouse, Rat samples.



- Using biophysical QC, antibody identity is confirmed at a molecular level for unrivalled batch-batch consistency


Images

Immunoprecipitation - Anti-Tau (phospho T181) antibody [EPR23506-107] (AB254409), expandable thumbnail
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Tau (phospho T181) antibody [EPR23506-107] (AB254409), expandable thumbnail
  • Immunohistochemistry (Frozen sections) - Anti-Tau (phospho T181) antibody [EPR23506-107] (AB254409), expandable thumbnail
  • Immunoprecipitation - Anti-Tau (phospho T181) antibody [EPR23506-107] (AB254409), expandable thumbnail
  • Western blot - Anti-Tau (phospho T181) antibody [EPR23506-107] (AB254409), expandable thumbnail

Publications

Key facts

Isotype
IgG
Host species
Rabbit
Storage buffer

Preservative: 0.01% Sodium azide
Constituents: 59.94% PBS, 40% Glycerol (glycerin, glycerine), 0.05% BSA

Form
Liquid
Clonality
Monoclonal

Immunogen

  • The exact immunogen used to generate this antibody is proprietary information.

Reactivity data

Select an application
Product promiseTestedExpectedPredictedNot recommended
ICC/IFIPI-ELISADotWBIHC-FrIHC-PAP
Human
Not recommended
Expected
Expected
Expected
Not recommended
Expected
Not recommended
Tested
Mouse
Not recommended
Tested
Expected
Expected
Tested
Tested
Tested
Expected
Rat
Not recommended
Tested
Expected
Expected
Tested
Tested
Tested
Expected
Synthetic peptide - Mouse
Not recommended
Not recommended
Tested
Tested
Not recommended
Not recommended
Not recommended
Not recommended

Not recommended
Not recommended

Species
Mouse
Dilution info
-
Notes

Perform heat-mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.

Species
Human
Dilution info
-
Notes

-

Species
Rat
Dilution info
-
Notes

-

Species
Synthetic peptide - Mouse
Dilution info
-
Notes

-

Tested
Tested

Species
Mouse
Dilution info
1/30
Notes

-

Species
Rat
Dilution info
1/30
Notes

-

Expected
Expected

Species
Human
Dilution info
Use at an assay dependent concentration.
Notes

-

Not recommended
Not recommended

Species
Synthetic peptide - Mouse
Dilution info
-
Notes

-

Tested
Tested

Species
Synthetic peptide - Mouse
Dilution info
-
Notes

Use at 62.5 ng /mL.

Expected
Expected

Species
Mouse, Rat, Human
Dilution info
Use at an assay dependent concentration.
Notes

-

Tested
Tested

Species
Synthetic peptide - Mouse
Dilution info
1/1000
Notes

-

Expected
Expected

Species
Mouse, Rat, Human
Dilution info
Use at an assay dependent concentration.
Notes

-

Tested
Tested

Species
Mouse
Dilution info
1/1000
Notes

-

Species
Rat
Dilution info
1/1000
Notes

-

Not recommended
Not recommended

Species
Human, Synthetic peptide - Mouse
Dilution info
-
Notes

-

Tested
Tested

Species
Mouse
Dilution info
1/50
Notes

Heat mediated antigen retrieval using sodium citrate buffer (10mM citrate pH 6.0 + 0.05% Tween-20).

Species
Rat
Dilution info
1/50
Notes

Heat mediated antigen retrieval using sodium citrate buffer (10mM citrate pH 6.0 + 0.05% Tween-20).

Expected
Expected

Species
Human
Dilution info
Use at an assay dependent concentration.
Notes

-

Not recommended
Not recommended

Species
Synthetic peptide - Mouse
Dilution info
-
Notes

-

Tested
Tested

Species
Mouse
Dilution info
1/5000
Notes

Perform heat-mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.

Species
Rat
Dilution info
1/5000
Notes

Perform heat-mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.

Not recommended
Not recommended

Species
Human
Dilution info
-
Notes

Perform heat-mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.

Species
Synthetic peptide - Mouse
Dilution info
-
Notes

-

Tested
Tested

Species
Human
Dilution info
-
Notes

Antibody concentration range - 6.67, 3.33, 1.67, 0.83, 0.42, 0 nM/mL

Expected
Expected

Species
Mouse, Rat
Dilution info
Use at an assay dependent concentration.
Notes

-

Not recommended
Not recommended

Species
Synthetic peptide - Mouse
Dilution info
-
Notes

-

Target data

Function

The protein expressed by the MAPT gene promotes microtubule assembly and stability and might be involved in establishing and maintaining neuronal polarity. Its C-terminus binds axonal microtubules, and the N-terminus binds neural plasma membrane components, suggesting that tau functions as a linker protein between the two. Axonal polarity is predetermined by MAPT localization within the neuronal cell's domain defined by the centrosome. The short isoforms allow cytoskeleton plasticity, whereas the longer isoforms may preferentially play a role in its stabilization. This supplementary information is collated from multiple sources and compiled automatically.

Additional Targets

MAPT phospho T181

Alternative names

Recommended products

Anti-Tau (phospho T181) antibody [EPR23506-107] (ab254409) is a rabbit monoclonal antibody that is used to detect Tau in Western Blot, IP, IHC-P, IHC-Fr, ELISA, Dot Blot. Suitable for Human, Mouse, Rat samples.



- Using biophysical QC, antibody identity is confirmed at a molecular level for unrivalled batch-batch consistency

Key facts

Isotype
IgG
Form
Liquid
Clonality
Monoclonal
Immunogen
  • The exact immunogen used to generate this antibody is proprietary information.
Clone number
EPR23506-107
Purification technique
Affinity purification Protein A
Specificity

The specificity of this antibody refers to P10636-8.

Dissociation constant
6.41 x 10-11 M
Concentration
Loading...

Storage

Shipped at conditions
Blue Ice
Appropriate short-term storage duration
1-2 weeks
Appropriate short-term storage conditions
+4°C
Appropriate long-term storage conditions
-20°C
Aliquoting information
Upon delivery aliquot
Storage information
Avoid freeze / thaw cycle

Notes

What is this antibody validated in?


Anti-Tau (phospho T181) antibody [EPR23506-107] (ab254409) is a rabbit recombinant monoclonal antibody and is validated for use in Western Blot (WB), Immunoprecipitation (IP), Immunohistochemistry (IHC-P), Immunohistochemistry (IHC-Fr), ELISA, Dot Blot in Human, Mouse, Rat samples.

What is the molecular weight of Tau?


Anti-Tau (phospho T181) [EPR23506-107] (ab254409) specifically detects a band for Tau (UniProt: P10636) at a molecular weight of 78kDa.

Trial sizes available!


Test your antibody or perform pre-screening before committing to a larger quantity. Sold in 10µl. Discover our selection of trial-size antibodies.

Other related products


We have a range of other formats of antibody clone [EPR23506-107] also available for your convenience:
ab254409, Carrier free - Anti-Tau (phospho T181) antibody [EPR23506-107] - BSA and Azide free ab277644, Alexa Fluor® 488 - Alexa Fluor® 488 Anti-Tau (phospho T181) antibody [EPR23506-107] ab309969, Alexa Fluor® 647 - Alexa Fluor® 647 Anti-Tau (phospho T181) antibody [EPR23506-107] ab309970, Biotin - Biotin Anti-Tau (phospho T181) antibody [EPR23506-107] ab314403



Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.

What are the advantages of a recombinant monoclonal antibody?
This product is a recombinant monoclonal antibody, which offers several advantages including:

  • - High batch-to-batch consistency and reproducibility
  • - Improved sensitivity and specificity
  • - Long-term security of supply
  • - Animal-free batch production

For more information, read more on recombinant antibodies.

Supplementary info

This supplementary information is collated from multiple sources and compiled automatically.
Activity summary

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.

Biological function summary

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.

Pathways

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.

Associated diseases and disorders

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.

Product promise

We are dedicated to supporting your work with high quality reagents and we are here for you every step of the way should you need us.

In the unlikely event of one of our products not working as expected, you are covered by our product promise.

Full details and terms and conditions can be found here:
Terms & Conditions.

11 product images

  • Immunoprecipitation - Anti-Tau (phospho T181) antibody [EPR23506-107] (ab254409), expandable thumbnail

    Immunoprecipitation - Anti-Tau (phospho T181) antibody [EPR23506-107] (ab254409)

    Tau (phospho T181) was immunoprecipitated from 0.35 mg of mouse brain tissue lysate with ab254409 at 1/30 dilution. Western blot was performed from the immunoprecipitate using ab254409 at 1/1000 dilution. VeriBlot for IP Detection Reagent (HRP)(VeriBlot for IP Detection Reagent (HRP) ab131366), was used as secondary antibody at 1/5000 dilution.

    Lane 1: Mouse brain tissue lysate 10μg (Input).
    Lane 2: ab254409 IP in mouse brain tissue lysate.
    Lane 3: Rabbit monoclonal IgG (Rabbit IgG, monoclonal [EPR25A] - Isotype Control ab172730) instead of ab254409 in mouse brain tissue lysate.

    Blocking and dilution buffer and concentration: 5% NFDM/TBST.
    Exposure time: 5.5 seconds.

    All lanes: Immunoprecipitation - Anti-Tau (phospho T181) antibody [EPR23506-107] (ab254409)

    Predicted band size: 47 kDa, 78 kDa

    Observed band size: 50-70 kDa

  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Tau (phospho T181) antibody [EPR23506-107] (ab254409), expandable thumbnail

    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Tau (phospho T181) antibody [EPR23506-107] (ab254409)

    Immunohistochemical analysis of paraffin-embedded mouse cerebrum tissue labeling Tau (phospho T181) with ab254409 at 1/5000 dilution, followed by Rabbit specific IHC polymer detection kit HRP/DAB (Rabbit specific IHC polymer detection kit HRP/DAB ab209101). Positive staining on mouse cerebrum without alkaline phosphatase treatment (image A). No signal was detected when tissues were treated with alkaline phosphatase (image B). Counter stained with hematoxylin.

    Secondary antibody only control: Used PBS instead of primary antibody, secondary antibody is Rabbit specific IHC polymer detection kit HRP/DAB (Rabbit specific IHC polymer detection kit HRP/DAB ab209101).

    Heat mediated antigen retrieval using Antigen Retrieval Buffer (100X Tris-EDTA Buffer, pH 9.0) ab93684 (Tris/EDTA buffer, pH 9.0).

  • Immunohistochemistry (Frozen sections) - Anti-Tau (phospho T181) antibody [EPR23506-107] (ab254409), expandable thumbnail

    Immunohistochemistry (Frozen sections) - Anti-Tau (phospho T181) antibody [EPR23506-107] (ab254409)

    Immunohistochemical analysis of frozen section of 4% PFA-fixed, 0.2% Triton X-100 permeabilized mouse cerebrum tissue labeling Tau (phospho T181) with ab254409 at 1/50 dilution, followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) at 1/1000 dilution (Green). Positive staining on mouse cerebrum without alkaline phosphatase treatment (image A). No signal was detected when tissues were treated with alkaline phosphatase (image B). The nuclear counterstain is DAPI (Blue).

    Secondary antibody only control: Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) at 1/1000 dilution.

  • Immunoprecipitation - Anti-Tau (phospho T181) antibody [EPR23506-107] (ab254409), expandable thumbnail

    Immunoprecipitation - Anti-Tau (phospho T181) antibody [EPR23506-107] (ab254409)

    Tau (phospho T181) was immunoprecipitated from 0.35 mg of rat brain tissue lysate with ab254409 at 1/30 dilution. Western blot was performed from the immunoprecipitate using ab254409 at 1/1000 dilution. VeriBlot for IP Detection Reagent (HRP)(VeriBlot for IP Detection Reagent (HRP) ab131366), was used as secondary antibody at 1/5000 dilution.

    Lane 1: Rat brain tissue lysate 10μg (Input).
    Lane 2: ab254409 IP in rat brain tissue lysate.
    Lane 3: Rabbit monoclonal IgG (Rabbit IgG, monoclonal [EPR25A] - Isotype Control ab172730) instead of ab254409 in rat brain tissue lysate.

    Blocking and dilution buffer and concentration: 5% NFDM/TBST.
    Exposure time: 10 seconds.

    All lanes: Immunoprecipitation - Anti-Tau (phospho T181) antibody [EPR23506-107] (ab254409)

    Predicted band size: 47 kDa, 78 kDa

    Observed band size: 50-70 kDa

  • Western blot - Anti-Tau (phospho T181) antibody [EPR23506-107] (ab254409), expandable thumbnail

    Western blot - Anti-Tau (phospho T181) antibody [EPR23506-107] (ab254409)

    Blocking and dilution buffer: 5% NFDM/TBST.

    Exposure time: 3 minutes.

    The molecular weight observed is consistent with what has been described in the literature (PMID: 21437732).

    This blot was developed using a higher sensitivity ECL substrate.

    All lanes: Western blot - Anti-Tau (phospho T181) antibody [EPR23506-107] (ab254409) at 1/1000 dilution

    Lane 1: Mouse brain tissue lysate at 20 µg

    Lane 2: Mouse brain tissue lysate (phosphatase treated membrane) at 20 µg

    Secondary

    All lanes: Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/100000 dilution

    Predicted band size: 47 kDa, 78 kDa

    Observed band size: 50-70 kDa

  • Western blot - Anti-Tau (phospho T181) antibody [EPR23506-107] (ab254409), expandable thumbnail

    Western blot - Anti-Tau (phospho T181) antibody [EPR23506-107] (ab254409)

    Blocking and dilution buffer: 5% NFDM/TBST.

    Exposure time: 3 minutes.

    The molecular weight observed is consistent with what has been described in the literature (PMID: 21437732).

    This blot was developed using a higher sensitivity ECL substrate.

    All lanes: Western blot - Anti-Tau (phospho T181) antibody [EPR23506-107] (ab254409) at 1/1000 dilution

    Lane 1: Rat brain tissue lysate at 20 µg

    Lane 2: Rat brain tissue lysate (phosphatase treated membrane) at 20 µg

    Secondary

    All lanes: Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/100000 dilution

    Predicted band size: 47 kDa, 78 kDa

    Observed band size: 50-70 kDa

  • Immunohistochemistry (Frozen sections) - Anti-Tau (phospho T181) antibody [EPR23506-107] (ab254409), expandable thumbnail

    Immunohistochemistry (Frozen sections) - Anti-Tau (phospho T181) antibody [EPR23506-107] (ab254409)

    Immunohistochemical analysis of frozen section of 4% PFA-fixed, 0.2% Triton X-100 permeabilized rat cerebrum tissue labeling Tau (phospho T181) with ab254409 at 1/50 dilution, followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) at 1/1000 dilution (Green). Positive staining on rat cerebrum without alkaline phosphatase treatment (image A). Nearly no signal was detected when tissues were treated with alkaline phosphatase (image B). The nuclear counterstain is DAPI (Blue).

    Secondary antibody only control: Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) at 1/1000 dilution.

  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Tau (phospho T181) antibody [EPR23506-107] (ab254409), expandable thumbnail

    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Tau (phospho T181) antibody [EPR23506-107] (ab254409)

    Immunohistochemical analysis of paraffin-embedded rat cerebrum tissue labeling Tau (phospho T181) with ab254409 at 1/5000 dilution, followed by Rabbit specific IHC polymer detection kit HRP/DAB (Rabbit specific IHC polymer detection kit HRP/DAB ab209101). Positive staining on rat cerebrum without alkaline phosphatase treatment (image A, PMID: 30279741). No signal was detected when tissues were treated with alkaline phosphatase (image B). Counter stained with hematoxylin.

    Secondary antibody only control: Used PBS instead of primary antibody, secondary antibody is Rabbit specific IHC polymer detection kit HRP/DAB (Rabbit specific IHC polymer detection kit HRP/DAB ab209101).

    Heat mediated antigen retrieval using Antigen Retrieval Buffer (100X Tris-EDTA Buffer, pH 9.0) ab93684 (Tris/EDTA buffer, pH 9.0).

  • Indirect ELISA - Anti-Tau (phospho T181) antibody [EPR23506-107] (ab254409), expandable thumbnail

    Indirect ELISA - Anti-Tau (phospho T181) antibody [EPR23506-107] (ab254409)

    Antigen: Mouse Tau non-phospho peptide,Mouse Tau (phospho T181) peptide.

    Antigen concentration: 1000 ng/mL.

    ab254409 used at 0 - 2000 ng/mL.

    Secondary antibody: Alkaline Phosphatase-conjugated AffiniPure Goat Anti-Rabbit IgG (H+L) at 1/2500 dilution.

  • Dot Blot - Anti-Tau (phospho T181) antibody [EPR23506-107] (ab254409), expandable thumbnail

    Dot Blot - Anti-Tau (phospho T181) antibody [EPR23506-107] (ab254409)

    Dot blot analysis of Tau (phospho T181) labeled with ab254409 at 1/1000 dilution.

    Lane 1: Tau (phospho T181) peptide (aa 177-190).
    Lane 2: Tau non-phospho peptide (aa 174-190).

    Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/100000 dilution was used as secondary antibody.

    Blocking and dilution buffer: 5% NFDM/TBST.

    Exposure time: 3 minutes.

  • Affinity Purification - Anti-Tau (phospho T181) antibody [EPR23506-107] (ab254409), expandable thumbnail

    Affinity Purification - Anti-Tau (phospho T181) antibody [EPR23506-107] (ab254409)

    Biotinylated Human Tau phospho T181 [0.5 μg/ml] was loaded to SA biosensor on Fortebio RED96e Machine, then associate with recombinant Anti-Tau (phospho T181) antibody [EPR23506-107] in serial concentration points [6.67, 3.33, 1.67, 0.83, 0.42 nM/mL] by 2-fold dilution, next to dissociate in blank testing buffer [0.1% BSA in PBST (0.05%Tween-20)]. Calculated signals had already subtracted blank control, curve fitting using 1:1 binding model. Non-phospho Tau protein's association and dissociation were also showed in graph. KD (M) value of Anti-Tau (phospho T181) antibody [EPR23506-107] is 6.41E-11

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Product protocols

For this product, it's our understanding that no specific protocols are required. You can:

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