重組人 Tau dGAE (297-391) 模擬AD前體原纖維 (無(wú)肝素輔助聚集)-自主發(fā)布-資訊-生物在線

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重組人 Tau dGAE (297-391) 模擬AD前體原纖維 (無(wú)肝素輔助聚集)

作者:欣博盛生物科技有限公司 暫無(wú)發(fā)布時(shí)間 (訪問(wèn)量:33839)

重組人 Tau dGAE (297-391) 模擬AD前體原纖維 (無(wú)肝素輔助聚集) Catalog No. SPR-502

 

產(chǎn)品詳情:

Product Name Tau dGAE (297-391) 模擬AD前體原纖維
Description

重組人 Tau dGAE (297-391) 模擬AD前體原纖維 (無(wú)肝素輔助聚集)

Applications WBSDS PAGEIn vitro Assay
Concentration 2 mg/ml 或 5 mg/ml
Conjugates 無(wú)標(biāo)簽
 
Nature 重組的
Species
Expression System 大腸桿菌 (E. coli)
Amino Acid Sequence IKHVPGGGSVQIVYKPVDLSKVTSKCGSLGNIHHKPGGGQVEVKSEKLDFKDRVQSKIGSLDNITHVPGGGNKKIETHKLTFRENAKAKTDHGAE
Purity >95%
Protein Length 野生型tau全長(zhǎng)蛋白 2N4R 的片段 (297 - 391aa)

 

Properties:

Storage Buffer 10mM PB pH 7.4, 10mM DTT, 200mM MgCl2
Storage Temperature -80ºC
Shipping Temperature 干冰. 運(yùn)輸: 該產(chǎn)品會(huì)與其他同訂單產(chǎn)品分開(kāi)發(fā)貨.
Purification 離子交換層析純化
Protein Size 10.165 kDa
Cite This Product Human Recombinant Tau dGAE (297-391) AD-mimic Pre-formed Fibrils (StressMarq Biosciences Inc., Victoria BC CANADA, Catalog # SPR-502)

Certificate Of Analysis

經(jīng)SDS-PAGE & Nanodrop分析驗(yàn)證蛋白純度 >95%.
Other Relevant Information 為達(dá)到最佳效果請(qǐng)?jiān)谑褂们俺曁幚? 請(qǐng)參考官網(wǎng)上神經(jīng)退行性疾病相關(guān)蛋白操作指南或產(chǎn)品說(shuō)明書. 單體來(lái)源是目錄號(hào)# SPR-316.

 

Biological Description:

Alternative NamesTau aggregate, Tau PFFs, Tau PFF, Tau protein aggregate, Tau protein, microtubule-associated protein Tau, MAPT, MAP, microtubule-associated protein, Truncated Tau Protein Aggregate, Paired Helical Filament-Tau, Phf-Tau, Neurofibrillary Tangle Protein, dGAE Tau Protein, Tau dGAEResearch AreasMT 相關(guān)蛋白, 神經(jīng)元標(biāo)記物, 神經(jīng)纖維纏結(jié)&Tau, 神經(jīng)退行性疾病, 細(xì)胞標(biāo)記物, 軸突標(biāo)記物, 微管, 神經(jīng)生物學(xué), 阿爾茨海默病, 細(xì)胞信號(hào)傳導(dǎo), 細(xì)胞骨架Swiss ProtP10636-8Scientific BackgroundFilamentous tau inclusions are a hallmark of many neurodegenerative diseases, including Alzheimer’s disease (AD) and Chronic Traumatic Encephalopathy (CTE), collectively called tauopathies. Advances in Cryo-EM have revealed that tau filaments isolated from individuals with a particular neurodegenerative disease share a distinct tau fold – i.e. an AD-isolated Tau filaments’ fold is distinct from a CTE-isolated Tau filaments’ fold (1-3). Utilizing Tau filaments with the correct disease-specific fold is an important goal towards better mimicking specific human diseases in cellular and in vivo models. Recent Cryo-EM studies have demonstrated that recombinantly generated Tau dGAE monomers will form the disease-isolated AD or CTE Tau filament folds under highly specific conditions in vitro (4, 5). StressMarq’s catalog# SPR-502 Tau dGAE (297-391) AD-mimic PFFs are purified and fibrilized under these exact published conditions that replicate the disease-isolated AD-fold (200 rpm at 37oC in 10 mM PB 10 mM DTT pH 7.4 200 mM MgCl2 for 48 hours).References1. Goedert, Eisenberg and Crowther. 2017. Propagation of Tau Aggregates and Neurodegeneration. Annu Rev Neurosci. 
2. Fitzpatrick et al. 2017. Cryo-EM structures of tau filaments from Alzheimer’s disease. Nature. 
3. Falcon et al. 2019. Novel tau filament fold in chronic traumatic encephalopathy encloses hydrophobic molecules. Nature. 
4. Lovestam et al. 2022. Assembly of Recombinant Tau into Filaments Identical to those of Alzheimer’s disease and Chronic Traumatic Encephalopathy. eLife. 
5. Lovestam et al. 2023. Disease-specific Tau Filaments Assemble via Polymorphic Intermediates. bioRxiv. 

 

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