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About PHF-Tau and Other Neuroscience Antibodies

What is Tau protein? What is PHF-tau?

Paired helical filament (PHF) is a major component of the neurofibrillary tangles involved in the pathology of Alzheimer’s disease. PHFs are composed of the microtubule-associated protein tau in a hyper-phosphorylated state (ref1). Tau protein is produced by a single gene expressed predominantly in neurons. The Tau gene undergoes complex alternative splicing, yielding six different isoforms of tau in the adult brain. Following translation, the tau protein can be further modified by phosphorylation at several different sites (refs2,3).

phf tau about#1

See complete product listing below!

Anti-PHF-tau Monoclonal Antibodies

Identification of hyperphosphorylated tau regions and the development of assays for early Alzheimer's diagnosis relies on phosphorylation-dependent monoclonal antibodies that recognize disease-specific phosphorylation patterns. Anti-PHF-tau antibody clone AT8 has been shown to detect PHF-tau doubly phosphorylated at Ser202 and Thr205, serines 199 and 202, and serines 205 and 208 (ref4). Anti-PHF-tau antibody AT8 has been used extensively to bind PHF-tau in neurofibrillary tangles in samples from Alzheimer's patients (refs4-7). Anti-PHF-tau antibody clones AT100, AT180, and AT270 have also been used successfully to stain neurofibrillary tangles containing PHF-tau (ref7). Clone AT180 recognizes PHF-tau phosphorylated at Thr231. Clone AT270 recognizes PHF-tau phosphorylated at Thr181. Use of these antibodies has demonstrated a significant increase in phosphorylation at these sites in Alzheimer's disease (ref3). Clone AT100 recognizes PHF-tau phosphorylated at Ser212 and Thr214.

Thermo Scientific Pierce Tau & PHF-tau Antibodie
Product Clone # Specificity Format Price
MN1020 AT8 PHF-tau (Ser202/Thr205)a Purified ¥85,000
MN1020B AT8 PHF-tau (Ser202/Thr205)a Biotin-labeled ¥85,000
MN1040 AT180 PHF-tau (Thr231) Purified ¥85,000
MN1040B AT180 PHF-tau (Thr231) Biotin-labeled ¥85,000
MN1050 AT270 PHF-tau (Thr181) Purified ¥88,000
MN1060 AT100 PHF-tau (Ser212/Thr214) Purified ¥88,000
MN1000 HT7 Tau Purified ¥43,000
MN1000B HT7 Tau Biotin-labeled ¥43,000
MN1010 BT2 Tau Purified ¥43,000
MN1010B BT2 Tau Biotin-labeled ¥43,000
PN1000 Sheep polyclonal Tau Purified ¥62,000

a AT8 was shown to be cross-reactive to doubly phosphorylated motifs containing either serine 199 and 202 or serine 205 and 208 (ref4).

Other Antibodies for Neuroscience
Product Clone # Specificity Format Price
MN1150 10H3 Beta Amyloid Purified ¥65,000
MN1150B 10H3 Beta Amyloid Biotin-labeled ¥65,000
MN1160 MID-N3, H14 γ-γ Enolase Purified ¥58,000
MN1080 NM4 GAP-43, B-50 Purified ¥65,000
MN1090 NM2 GAP-43, B-50 Purified ¥65,000
MN1180 MIG-G2 GFAP: Glial Fibrillary Acidic Protein Purified ¥65,000
MN1190 MIG-N18 Neurofilament (Ser) Purified ¥28,000
MN1250 2B10 Rab3a Purified ¥55,000
MN1280 11D2 SNAP25 Purified ¥55,000
MN1270 15C2 Synapsin Purified ¥55,000
MN1260 5C8 Synapsin Purified ¥55,000
MN1290 9B6 Synapsin Purified ¥55,000
MN1170 MIG-T4, NFT200 Tangles Purified ¥62,000

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参考文献

  1. Goedert, M. (1996). Tau protein and the neurofibrillary pathology of Alzheimer’s disease. Ann. N. Y. Acad. Sci. 777: 121-131.
  2. Kosik, K.S. (1990). Tau protein and neurodegeneration. Mol. Neurobiol. 4(3-4): 171-179.
  3. Goedert, M., et al. (1994). Epitope mapping of monoclonal antibodies to the paired helical filaments of Alzheimer’s disease: identification of phosphorylation sites in tau protein. Biochem. J. 301(Pt 3): 871-877.
  4. Porzig, R., et al. (2007). Epitope mapping of mAbs AT8 and Tau5 directed against hyperphosphorylated regions of the human tau protein. Biochem. Biophys. Res. Commun. 358(2): 644-649.
  5. Arima, K., et al. (2000). NACP/alpha-synuclein and tau constitute two distinctive subsets of filaments in the same neuronal inclusions in brains from a family of parkinsonism and dementia with Lewy bodies: double-immunolabeling fluorescence and electron microscope studies. Acta Neuropathol. 100(2): 115-121.
  6. Uchihara, T., et al. (2001). Evolution from pretangle neurons to neurofibrillary tangles monitored by thiazen red combined with Gallyas method and double immunofluorescence. Acta Neuropathol. 101(6): 535-539.
  7. Spillantini, M. G., et al. (1996). Comparison of the neurofibrillary pathology in Alzheimer’s disease and familial presenile dementia with tangles. Acta Neuropathol. 92(1): 42-48.