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xenocs xsact software  (Xenocs Inc)


Bioz Verified Symbol Xenocs Inc is a verified supplier
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    Xenocs Inc xenocs xsact software
    Xenocs Xsact Software, supplied by Xenocs Inc, used in various techniques. Bioz Stars score: 96/100, based on 210 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/data+analysis/XSACT+Pro/pmc10517254-485-4-4
    Average 96 stars, based on 210 article reviews
    xenocs xsact software - by Bioz Stars, 2026-09
    96/100 stars

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    Software:

    Article Title: Revisiting the anisotropic complex refractive indices of sodium nitrate for interpretation of the reflectance spectra of pressed pellets
    Article Snippet: .. Data were acquired at four detector positions, each with an exposure time of 300 s. Initial data analysis was completed using the Xenocs XSACT software package. ..

    Article Title: Bioelectronic skin-conducting polymer interface: Assessing the role of nanopores and appendages
    Article Snippet: .. Azimuthal integration of the 2D patterns provided the 1D diffraction curves, which were corrected for background scattering and normalized to the direct beam, using the Xenocs XSACT software (version 2.6). ..

    Article Title: Polar solvent strategy enables scalable synthesis of perovskite nanocrystal scintillators for fast X-ray imaging.
    Article Snippet: The measuring time was set to 7,200 s. Frames were taken with a Dectris Eiger2 4M detector, and data processing steps, including background correction (electronic noise), cosmic radiation elimination, and 2D to 1D integration, were performed subsequently. .. The data were viewed and analyzed using the grazing incidence module of the Xenocs XSACT software. .. The CsPbBr3 PL spectra were excited using a 150 W Xe lamp and collected using a FluoroMax+ fluorescence spectrometer (Horiba Scientific).



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    Image Search Results


    Cytokine expression profile after AAV gene therapy in NHPs Quantification of vitreous cytokines in NHP1 (A) and NHP2 (B) using the LegendPlex NHP Inflammation Panel with levels expressed as fold-change (log 2) in mean fluorescence intensity (MFI) relative to baseline. RE, right eyes; LE, left eye. (C and D) Single-cell transcriptomic analysis of cytokine gene expression among retinal cell types in NHP1 and NHP2, respectively.

    Journal: Molecular Therapy Advances

    Article Title: Single-cell and spatial transcriptomic analyses of gene therapy-associated retinal inflammation in non-human primates

    doi: 10.1016/j.omta.2026.201726

    Figure Lengend Snippet: Cytokine expression profile after AAV gene therapy in NHPs Quantification of vitreous cytokines in NHP1 (A) and NHP2 (B) using the LegendPlex NHP Inflammation Panel with levels expressed as fold-change (log 2) in mean fluorescence intensity (MFI) relative to baseline. RE, right eyes; LE, left eye. (C and D) Single-cell transcriptomic analysis of cytokine gene expression among retinal cell types in NHP1 and NHP2, respectively.

    Article Snippet: Data were analyzed in the LEGENDplex Data Analysis Software (Qognit, BioLegend).

    Techniques: Expressing, Fluorescence, Single Cell, Gene Expression