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hr tem  (JEOL)


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    Structured Review

    JEOL hr tem
    Development of GME method. SEM images of a) AuS@CuO substrate and b) AuS@CuO after GME in the presence of target analytes, <t>c)</t> <t>HR‐TEM</t> and TEM (inset) images of the AuNS on the AuS@CuO in the presence of target analytes, d) elemental mapping on the TEM image area, e) SERS enhancement in GME development, f) real‐time time monitoring of SERS signal changes at 1600 cm −1 and g) time‐resolved spectral evolution during GME, and h) SERS activity of GME for 4‐aminothiophenol and benzoic acid detection on the AuS and AuS@CuO substrate.
    Hr Tem, supplied by JEOL, used in various techniques. Bioz Stars score: 97/100, based on 9646 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/electron+microscope/JEM-2200FS+Transmission+Electron+Microscope/pmc13181542-333-19-24
    Average 97 stars, based on 9646 article reviews
    hr tem - by Bioz Stars, 2026-10
    97/100 stars

    Images

    1) Product Images from "Label‐Free SERS Fingerprinting of Neuroprotein Conformational Dynamics in Human Saliva"

    Article Title: Label‐Free SERS Fingerprinting of Neuroprotein Conformational Dynamics in Human Saliva

    Journal: Advanced Materials (Deerfield Beach, Fla.)

    doi: 10.1002/adma.202513500

    Development of GME method. SEM images of a) AuS@CuO substrate and b) AuS@CuO after GME in the presence of target analytes, c) HR‐TEM and TEM (inset) images of the AuNS on the AuS@CuO in the presence of target analytes, d) elemental mapping on the TEM image area, e) SERS enhancement in GME development, f) real‐time time monitoring of SERS signal changes at 1600 cm −1 and g) time‐resolved spectral evolution during GME, and h) SERS activity of GME for 4‐aminothiophenol and benzoic acid detection on the AuS and AuS@CuO substrate.
    Figure Legend Snippet: Development of GME method. SEM images of a) AuS@CuO substrate and b) AuS@CuO after GME in the presence of target analytes, c) HR‐TEM and TEM (inset) images of the AuNS on the AuS@CuO in the presence of target analytes, d) elemental mapping on the TEM image area, e) SERS enhancement in GME development, f) real‐time time monitoring of SERS signal changes at 1600 cm −1 and g) time‐resolved spectral evolution during GME, and h) SERS activity of GME for 4‐aminothiophenol and benzoic acid detection on the AuS and AuS@CuO substrate.

    Techniques Used: Activity Assay

    Material and optical characterization of GME in the presence of protein. a) SEM image of AuS@CuO after GME, b) HR‐TEM image of the AuS‐CuO‐AuNS interfaces area, c) schematic illustration of GME mechanism for protein detection, d) elemental mapping of the corresponding HR‐TEM image area, e) E‐field distribution of GME, f) UV–vis absorbance spectra of AuS@CuO before and after GME in both presence and absence of protein, g) SERS enhancement of GME method for protein detection (scale bar refers to SERS intensity), h) SERS performance of the GME method at various cyt c concentrations, i) signal uniformity test with 100 different points, j) reproducibility test with 5 independent test for each batch, k) stability test of GME at various storage time.
    Figure Legend Snippet: Material and optical characterization of GME in the presence of protein. a) SEM image of AuS@CuO after GME, b) HR‐TEM image of the AuS‐CuO‐AuNS interfaces area, c) schematic illustration of GME mechanism for protein detection, d) elemental mapping of the corresponding HR‐TEM image area, e) E‐field distribution of GME, f) UV–vis absorbance spectra of AuS@CuO before and after GME in both presence and absence of protein, g) SERS enhancement of GME method for protein detection (scale bar refers to SERS intensity), h) SERS performance of the GME method at various cyt c concentrations, i) signal uniformity test with 100 different points, j) reproducibility test with 5 independent test for each batch, k) stability test of GME at various storage time.

    Techniques Used:

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    Microscopy:

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    X-ray Spectroscopy:

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    Electron Microscopy:

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    Scanning Electron Microscopy:

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    Spectroscopy:

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    Transmission Electron Microscopy:

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    High-Resolution TEM:

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    Transmission Assay:

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    Silicon Carbide:

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    Sample Prep:

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    Suspension:

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    Scanning Transmission Electron Microscopy:

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    Silicon:

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    Cryo-TEM:

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    Förster Resonance Energy Transfer:

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    Synthesized:

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    Dynamic Light Scattering Assay:

    Article Title: Structural tuning of galactomannan-poly(ε-caprolactone) nanocapsule hybrid hydrogels mediated by 1,2,3,4-butanetetracarboxylic acid.
    Article Snippet: ith liquid nitrogen. Afterward, the grids were carefully moved to a cryo transfer and tomography holder (Fischione Model 2550, E.A. Fischione Instruments, Pittsburgh). To capture images, we employed a JEOL JEM2200FS electron microscope (JEOL, Freising, Germany) equipped with a cold field-emission electron gun. The microscope operated at an acceleration voltage of 200 kV, and the resulting images we

    In Vivo:

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    Article Snippet: ith liquid nitrogen. Afterward, the grids were carefully moved to a cryo transfer and tomography holder (Fischione Model 2550, E.A. Fischione Instruments, Pittsburgh). To capture images, we employed a JEOL JEM2200FS electron microscope (JEOL, Freising, Germany) equipped with a cold field-emission electron gun. The microscope operated at an acceleration voltage of 200 kV, and the resulting images we

    Generated:

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    Article Snippet: ith liquid nitrogen. Afterward, the grids were carefully moved to a cryo transfer and tomography holder (Fischione Model 2550, E.A. Fischione Instruments, Pittsburgh). To capture images, we employed a JEOL JEM2200FS electron microscope (JEOL, Freising, Germany) equipped with a cold field-emission electron gun. The microscope operated at an acceleration voltage of 200 kV, and the resulting images we

    Produced:

    Article Title: Structural tuning of galactomannan-poly(ε-caprolactone) nanocapsule hybrid hydrogels mediated by 1,2,3,4-butanetetracarboxylic acid.
    Article Snippet: ith liquid nitrogen. Afterward, the grids were carefully moved to a cryo transfer and tomography holder (Fischione Model 2550, E.A. Fischione Instruments, Pittsburgh). To capture images, we employed a JEOL JEM2200FS electron microscope (JEOL, Freising, Germany) equipped with a cold field-emission electron gun. The microscope operated at an acceleration voltage of 200 kV, and the resulting images we



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