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high content imaging station scanr  (Evident Corporation)

 
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    Evident Corporation high content imaging station scanr
    High Content Imaging Station Scanr, supplied by Evident Corporation, 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/scanr+high+content+imaging+system/scanR+High-Content+Screening+Station+for+Life+Science/pm40269950-312-9-13
    Average 95 stars, based on 1 article reviews
    high content imaging station scanr - by Bioz Stars, 2026-09
    95/100 stars

    Images

    Related Articles

    Immunofluorescence:

    Article Title: Biallelic PARP1 Mutations Associated with Childhood-Onset Neurodegeneration
    Article Snippet: .. Numbers of γH2AX foci per cell and poly/mono ADP-ribose immunofluorescence were quantified using an Olympus ScanR high-content imaging system with ScanR Image Acquisition and Analysis Software. ..

    Imaging:

    Article Title: Biallelic PARP1 Mutations Associated with Childhood-Onset Neurodegeneration
    Article Snippet: .. Numbers of γH2AX foci per cell and poly/mono ADP-ribose immunofluorescence were quantified using an Olympus ScanR high-content imaging system with ScanR Image Acquisition and Analysis Software. ..

    Article Title: Small molecules blocking histone reader domains
    Article Snippet: Cells were washed 3 times and DNA was counterstained with DAPI (Sigma). .. Images were acquired on ScanR high-content imaging system (Olympus) and analysed using ScanR software. .. Relative fluorescence intensity TONSL was quantified relative to cells depleted for TONSL using the specific siRNAs (O'Donnell et al. 2010 Mol Cel 40:619, synthesized by Sigma) for 30 h at 100 nM concentration.

    Software:

    Article Title: Biallelic PARP1 Mutations Associated with Childhood-Onset Neurodegeneration
    Article Snippet: .. Numbers of γH2AX foci per cell and poly/mono ADP-ribose immunofluorescence were quantified using an Olympus ScanR high-content imaging system with ScanR Image Acquisition and Analysis Software. ..

    Article Title: Small molecules blocking histone reader domains
    Article Snippet: Cells were washed 3 times and DNA was counterstained with DAPI (Sigma). .. Images were acquired on ScanR high-content imaging system (Olympus) and analysed using ScanR software. .. Relative fluorescence intensity TONSL was quantified relative to cells depleted for TONSL using the specific siRNAs (O'Donnell et al. 2010 Mol Cel 40:619, synthesized by Sigma) for 30 h at 100 nM concentration.



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    (A) , representative single-cell galleries ( top ) and quantification ( bottom ) of <t>nuclear</t> <t>ADP-ribose</t> levels before and after treatment of cells with H 2 O 2 , from <t>scanR</t> high-content imaging. Quantified data are the mean (+/-1SD) ADP-ribose fluorescence from five independent experiments, with >1000 cells scored per sample per experiment. (B) , Quantification of endogenous ADP-ribose levels in S phase cells following, where indicated, incubation with PARG inhibitor (+PARGi) for 60 min to preserve nascent poly (ADP-ribose). Data were quantified as described above, from three independent experiments. Only significant differences are shown (*p≤0.05; ***p≤0.001), determined by 2-way ANOVA with Sidak’s multiple comparisons test.
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    (A) , representative single-cell galleries ( top ) and quantification ( bottom ) of <t>nuclear</t> <t>ADP-ribose</t> levels before and after treatment of cells with H 2 O 2 , from <t>scanR</t> high-content imaging. Quantified data are the mean (+/-1SD) ADP-ribose fluorescence from five independent experiments, with >1000 cells scored per sample per experiment. (B) , Quantification of endogenous ADP-ribose levels in S phase cells following, where indicated, incubation with PARG inhibitor (+PARGi) for 60 min to preserve nascent poly (ADP-ribose). Data were quantified as described above, from three independent experiments. Only significant differences are shown (*p≤0.05; ***p≤0.001), determined by 2-way ANOVA with Sidak’s multiple comparisons test.
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    Image Search Results


    (A) , representative single-cell galleries ( top ) and quantification ( bottom ) of nuclear ADP-ribose levels before and after treatment of cells with H 2 O 2 , from scanR high-content imaging. Quantified data are the mean (+/-1SD) ADP-ribose fluorescence from five independent experiments, with >1000 cells scored per sample per experiment. (B) , Quantification of endogenous ADP-ribose levels in S phase cells following, where indicated, incubation with PARG inhibitor (+PARGi) for 60 min to preserve nascent poly (ADP-ribose). Data were quantified as described above, from three independent experiments. Only significant differences are shown (*p≤0.05; ***p≤0.001), determined by 2-way ANOVA with Sidak’s multiple comparisons test.

    Journal: medRxiv

    Article Title: Biallelic PARP1 Mutations Associated with Childhood-Onset Neurodegeneration

    doi: 10.1101/2023.06.09.23291078

    Figure Lengend Snippet: (A) , representative single-cell galleries ( top ) and quantification ( bottom ) of nuclear ADP-ribose levels before and after treatment of cells with H 2 O 2 , from scanR high-content imaging. Quantified data are the mean (+/-1SD) ADP-ribose fluorescence from five independent experiments, with >1000 cells scored per sample per experiment. (B) , Quantification of endogenous ADP-ribose levels in S phase cells following, where indicated, incubation with PARG inhibitor (+PARGi) for 60 min to preserve nascent poly (ADP-ribose). Data were quantified as described above, from three independent experiments. Only significant differences are shown (*p≤0.05; ***p≤0.001), determined by 2-way ANOVA with Sidak’s multiple comparisons test.

    Article Snippet: Numbers of γH2AX foci per cell and poly/mono ADP-ribose immunofluorescence were quantified using an Olympus ScanR high-content imaging system with ScanR Image Acquisition and Analysis Software.

    Techniques: Imaging, Fluorescence, Incubation