Tau Antibody,StressMarq Biosciences Inc.,SPC-806D

Rabbit Anti-Human Truncated Tau dGAE (297-391) Polyclonal

Host

Rabbit

Reactivity

Human, Mouse, Rat

Application

WB

Conjugate

APC, ATTO 390, ATTO 488, ATTO 594, Biotin, FITC, HRP, PerCP, RPE, Unconjugated

Platform ID

BAB402594691

StressMarq Biosciences Inc.

Headquarters

118-1537 Hillside Avenue, Victoria, British Columbia, V8T 4Y2, CANADA

Contact

Tel: +1 250-294-9065
Fax: +1 250-294-9025

Product Specifications
Scientific Background
Synonyms

Specifications

NameTau Antibody
Cat. No.SPC-806D
Accession NumberP10636
Gene ID (Entrez)4137
HostRabbit
RRIDAB_3716851)
ReactivityHuman, Mouse, Rat
ConjugationAPC, ATTO 390, ATTO 488, ATTO 594, Biotin, FITC, HRP, PerCP, RPE, Unconjugated
ApplicationWB
Working DilutionsWB (1:1000); optimal dilutions for assays should be determined by the user.
ClonalityPolyclonal
Concentration1mg/mL
ImmunogenRecombinant Human Tau AA297-391 (dGAE) Fibril (SPR-461)
PurityProtein A
ShippingBlue Ice or 4ºC
FormulationPBS pH 7.4, 50% glycerol, 0.09% sodium azide *Storage buffer may change when conjugated
Storage-20ºC, Conjugated antibodies should be stored according to the product label

Scientific Background

Tau is a microtubule-associated protein encoded by the MAPT gene and plays a vital role in stabilizing neuronal microtubules. In Alzheimer’s disease (AD) and related tauopathies, tau undergoes pathological modifications that lead to its aggregation into paired helical filaments (PHFs), forming neurofibrillary tangles—a hallmark of AD. A truncated tau fragment comprising residues 297–391, known as Tau dGAE, represents a minimal core region capable of self-assembling into PHF-like fibrils in vitro without the need for cofactors or templates. This 95-amino acid segment has been identified in the core of PHFs extracted from AD brain tissue and forms filaments that closely mimic those observed in human pathology. Tau dGAE is a powerful model for studying the molecular mechanisms of tau aggregation, seeding, and propagation. Its ability to recapitulate key structural features of pathological tau makes it an essential tool for developing aggregation inhibitors, imaging agents, and immunotherapies targeting tau fibrils. By isolating the aggregation-prone core of tau, researchers can dissect the structural transitions and biochemical interactions that drive neurodegeneration, making Tau dGAE a critical focus in Alzheimer’s disease research and therapeutic development.

Synonyms

Tau, MAPT, Microtubule-associated protein tau, Microtubule associated protein tau, Microtubule associated protein tau isoform 4, TAU_HUMAN, TAU, MAPTL, MTBT1, MTBT2, RNPTAU, PHF-tau, PHF tau, Paired helical filament tau, Paired helical filament-tau, Neurofibrillary tangle protein, DDPAC, FTDP 17, MSTD, PPND, PPP1R103, Protein phosphatase 1 regulatory subunit 103, G protein beta1/gamma2 subunit interacting factor 1, AI413597, AW045860, FLJ31424, MGC134287, MGC138549, MGC156663, dGAE tau fibril, Truncated Tau Fragment (AA297-391), 95-amino acid tau protein fragment, Truncated Tau Protein

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