WB result of Tau (phospho T217) Recombinant Rabbit mAb
Blocking/Diluting buffer and concentration: 5% BSA/TBST
Primary antibody: Tau (phospho T217) Recombinant Rabbit mAb at 1/1000 dilution
Lane 1: old mouse brain lysate 20 µg
Lane 2: phosphatase treated old mouse brain 20 µg
Secondary antibody: Goat Anti-rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 46 kDa
Observed MW: 38-80 kDa
Product Details
Product Details
Product Specification
Host | Rabbit |
Antigen | Tau (phospho T217) |
Synonyms | Microtubule-associated protein tau; Neurofibrillary tangle protein; Paired helical filament-tau (PHF-tau); MAPTL; MTBT1; TAU; MAPT |
Immunogen | Synthetic Peptide |
Location | Cytoplasm, Cytoskeleton, Secreted, Cell membrane, Endoplasmic reticulum |
Accession | P10636-8 |
Clone Number | S-176-213 |
Antibody Type | Recombinant mAb |
Isotype | IgG |
Application | WB |
Reactivity | Hu, Ms, Rt |
Purification | Protein A |
Concentration | 0.5 mg/ml |
Conjugation | Unconjugated |
Physical Appearance | Liquid |
Storage Buffer | PBS, 40% Glycerol, 0.05% BSA, 0.03% Proclin 300 |
Stability & Storage | 12 months from date of receipt / reconstitution, -20 °C as supplied |
Dilution
application | dilution | species |
Dot Blot | 1:1000 | |
WB | 1:1000 | Ms, Rt |
Background
Tau (phospho T217) refers to a specific form of the Tau protein that has undergone phosphorylation at its 217th threonine residue. This modification has been recognized as a highly promising biomarker for Alzheimer's disease (AD) and other tauopathies. In healthy neurons, Tau protein stabilizes the cytoskeleton by binding to microtubules, and its function is tightly regulated by phosphorylation levels. However, under pathological conditions, hyperphosphorylation at sites such as T217 significantly impairs Tau's ability to bind to microtubules, leading to its misfolding, aggregation, and ultimately the formation of neurofibrillary tangles—one of the core pathological hallmarks of AD. Notably, phosphorylation at T217 is markedly elevated in the very early stages of the disease, even before symptoms appear, and its abnormal levels closely correlate with the distribution of tangles and cognitive decline. Due to its high specificity and sensitivity, detection methods such as cerebrospinal fluid assays and emerging positron emission tomography (PET) imaging are currently being utilized to measure Tau (phospho T217), aiming to achieve early and accurate diagnosis of AD as well as monitoring of disease progression.
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Picture
Western Blot
WB result of Tau (phospho T217) Recombinant Rabbit mAb
Blocking/Diluting buffer and concentration: 5% BSA/TBST
Primary antibody: Tau (phospho T217) Recombinant Rabbit mAb at 1/1000 dilution
Lane 1: rat brain lysate 20 µg
Lane 2: phosphatase treated rat brain 20 µg
Secondary antibody: Goat Anti-rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 46 kDa
Observed MW: 38-65 kDa
Dot Blot
Dot blot result of Tau (phospho T217) Recombinant Rabbit mAb
Lane 1: phospho Tau217 peptide
Lane 2: phospho Tau217 peptide (different sequence from lane 1 peptide)
Lane 3: non-phospho Tau217 peptide
Primary antibody: Tau (phospho T217) Recombinant Rabbit mAb at 1/1000 dilution
Secondary antibody: Goat Anti-rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
