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sspe case 2  (Thermo Fisher)


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    Structured Review

    Thermo Fisher sspe case 2
    Immunolabelling and immunoblotting of tau filaments from SSPE. a , b Immunoelectron microscopy of filaments from SSPE cases 1 ( a ) and 2 ( b ) using anti-tau antibody AT8. c Immunoblotting of sarkosyl-insoluble fractions using anti-tau antibodies: Tau N; AT8; RD3; Anti-4R; Tau354; T46. Lanes: 1, SSPE case 1; 2, SSPE case 2; 3, AD
    Sspe Case 2, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/sspe+case+2/pmc10161654-73-6-12?v=Thermo+Fisher
    Average 95 stars, based on 1 article reviews
    sspe case 2 - by Bioz Stars, 2026-08
    95/100 stars

    Images

    1) Product Images from "Identical tau filaments in subacute sclerosing panencephalitis and chronic traumatic encephalopathy"

    Article Title: Identical tau filaments in subacute sclerosing panencephalitis and chronic traumatic encephalopathy

    Journal: Acta Neuropathologica Communications

    doi: 10.1186/s40478-023-01565-2

    Immunolabelling and immunoblotting of tau filaments from SSPE. a , b Immunoelectron microscopy of filaments from SSPE cases 1 ( a ) and 2 ( b ) using anti-tau antibody AT8. c Immunoblotting of sarkosyl-insoluble fractions using anti-tau antibodies: Tau N; AT8; RD3; Anti-4R; Tau354; T46. Lanes: 1, SSPE case 1; 2, SSPE case 2; 3, AD
    Figure Legend Snippet: Immunolabelling and immunoblotting of tau filaments from SSPE. a , b Immunoelectron microscopy of filaments from SSPE cases 1 ( a ) and 2 ( b ) using anti-tau antibody AT8. c Immunoblotting of sarkosyl-insoluble fractions using anti-tau antibodies: Tau N; AT8; RD3; Anti-4R; Tau354; T46. Lanes: 1, SSPE case 1; 2, SSPE case 2; 3, AD

    Techniques Used: Western Blot, Immuno-Electron Microscopy

    Cryo-EM cross-sections and structures of tau filaments from SSPE. a Cross-sections through the cryo-EM reconstructions, perpendicular to the helical thickness and with a projected thickness of approximately one rung, are shown for SSPE cases 1 and 2. A majority of Type I and a minority of Type II tau filaments are each made of two copies of a single protofilament arranged in different ways (ultrastructural polymorphs). Resolutions and filament percentages: SSPE case 1: Type I CTE filament 2.3 Å, 92%; Type II CTE filament 5.1 Å, 8%. SSPE case 2: Type I CTE filament 3.0 Å, 91%; Type II CTE filament 3.5 Å, 9%. Scale bar, 5 nm. b Cryo-EM density maps (grey transparent) of SSPE Type I and Type II tau filaments and the atomic models coloured blue (Type I) and orange (Type II). c SSPE Type I (blue) and Type II (orange) filaments overlaid with CTE Type I (magenta) and CTE Type II (magenta) filaments. The filament core extends from tau residues K274/S305-R379
    Figure Legend Snippet: Cryo-EM cross-sections and structures of tau filaments from SSPE. a Cross-sections through the cryo-EM reconstructions, perpendicular to the helical thickness and with a projected thickness of approximately one rung, are shown for SSPE cases 1 and 2. A majority of Type I and a minority of Type II tau filaments are each made of two copies of a single protofilament arranged in different ways (ultrastructural polymorphs). Resolutions and filament percentages: SSPE case 1: Type I CTE filament 2.3 Å, 92%; Type II CTE filament 5.1 Å, 8%. SSPE case 2: Type I CTE filament 3.0 Å, 91%; Type II CTE filament 3.5 Å, 9%. Scale bar, 5 nm. b Cryo-EM density maps (grey transparent) of SSPE Type I and Type II tau filaments and the atomic models coloured blue (Type I) and orange (Type II). c SSPE Type I (blue) and Type II (orange) filaments overlaid with CTE Type I (magenta) and CTE Type II (magenta) filaments. The filament core extends from tau residues K274/S305-R379

    Techniques Used: Cryo-EM Sample Prep



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    Thermo Fisher sspe case 2
    Immunolabelling and immunoblotting of tau filaments from SSPE. a , b Immunoelectron microscopy of filaments from SSPE cases 1 ( a ) and 2 ( b ) using anti-tau antibody AT8. c Immunoblotting of sarkosyl-insoluble fractions using anti-tau antibodies: Tau N; AT8; RD3; Anti-4R; Tau354; T46. Lanes: 1, SSPE case 1; 2, SSPE case 2; 3, AD
    Sspe Case 2, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/sspe+case+2/pmc10161654-73-6-12?v=Thermo+Fisher
    Average 95 stars, based on 1 article reviews
    sspe case 2 - by Bioz Stars, 2026-08
    95/100 stars
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    Immunolabelling and immunoblotting of tau filaments from SSPE. a , b Immunoelectron microscopy of filaments from SSPE cases 1 ( a ) and 2 ( b ) using anti-tau antibody AT8. c Immunoblotting of sarkosyl-insoluble fractions using anti-tau antibodies: Tau N; AT8; RD3; Anti-4R; Tau354; T46. Lanes: 1, SSPE case 1; 2, SSPE case 2; 3, AD

    Journal: Acta Neuropathologica Communications

    Article Title: Identical tau filaments in subacute sclerosing panencephalitis and chronic traumatic encephalopathy

    doi: 10.1186/s40478-023-01565-2

    Figure Lengend Snippet: Immunolabelling and immunoblotting of tau filaments from SSPE. a , b Immunoelectron microscopy of filaments from SSPE cases 1 ( a ) and 2 ( b ) using anti-tau antibody AT8. c Immunoblotting of sarkosyl-insoluble fractions using anti-tau antibodies: Tau N; AT8; RD3; Anti-4R; Tau354; T46. Lanes: 1, SSPE case 1; 2, SSPE case 2; 3, AD

    Article Snippet: Lanes: 1, SSPE case 1; 2, SSPE case 2; 3, AD By cryo-EM, we show that the CTE fold of assembled tau is characteristic of SSPE cases 1 and 2 (Fig. ; Additional file : Figure S1).

    Techniques: Western Blot, Immuno-Electron Microscopy

    Cryo-EM cross-sections and structures of tau filaments from SSPE. a Cross-sections through the cryo-EM reconstructions, perpendicular to the helical thickness and with a projected thickness of approximately one rung, are shown for SSPE cases 1 and 2. A majority of Type I and a minority of Type II tau filaments are each made of two copies of a single protofilament arranged in different ways (ultrastructural polymorphs). Resolutions and filament percentages: SSPE case 1: Type I CTE filament 2.3 Å, 92%; Type II CTE filament 5.1 Å, 8%. SSPE case 2: Type I CTE filament 3.0 Å, 91%; Type II CTE filament 3.5 Å, 9%. Scale bar, 5 nm. b Cryo-EM density maps (grey transparent) of SSPE Type I and Type II tau filaments and the atomic models coloured blue (Type I) and orange (Type II). c SSPE Type I (blue) and Type II (orange) filaments overlaid with CTE Type I (magenta) and CTE Type II (magenta) filaments. The filament core extends from tau residues K274/S305-R379

    Journal: Acta Neuropathologica Communications

    Article Title: Identical tau filaments in subacute sclerosing panencephalitis and chronic traumatic encephalopathy

    doi: 10.1186/s40478-023-01565-2

    Figure Lengend Snippet: Cryo-EM cross-sections and structures of tau filaments from SSPE. a Cross-sections through the cryo-EM reconstructions, perpendicular to the helical thickness and with a projected thickness of approximately one rung, are shown for SSPE cases 1 and 2. A majority of Type I and a minority of Type II tau filaments are each made of two copies of a single protofilament arranged in different ways (ultrastructural polymorphs). Resolutions and filament percentages: SSPE case 1: Type I CTE filament 2.3 Å, 92%; Type II CTE filament 5.1 Å, 8%. SSPE case 2: Type I CTE filament 3.0 Å, 91%; Type II CTE filament 3.5 Å, 9%. Scale bar, 5 nm. b Cryo-EM density maps (grey transparent) of SSPE Type I and Type II tau filaments and the atomic models coloured blue (Type I) and orange (Type II). c SSPE Type I (blue) and Type II (orange) filaments overlaid with CTE Type I (magenta) and CTE Type II (magenta) filaments. The filament core extends from tau residues K274/S305-R379

    Article Snippet: Lanes: 1, SSPE case 1; 2, SSPE case 2; 3, AD By cryo-EM, we show that the CTE fold of assembled tau is characteristic of SSPE cases 1 and 2 (Fig. ; Additional file : Figure S1).

    Techniques: Cryo-EM Sample Prep