hr tem (JEOL)
97
Structured Review
JEOL
hr tem

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, 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
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
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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