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incucyte software analysis  (Sartorius AG)


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    Structured Review

    Sartorius AG incucyte software analysis

    Incucyte Software Analysis, supplied by Sartorius AG, used in various techniques. Bioz Stars score: 99/100, based on 16037 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/live+cell+analysis+instruments/Live+Cell+Analysis+Instruments/pmc13657218-36-0-4
    Average 99 stars, based on 16037 article reviews
    incucyte software analysis - by Bioz Stars, 2026-10
    99/100 stars

    Images

    1) Product Images from "Species-specific inflammatory responses of chondrocytes: Toward evidence-based model selection in OA research"

    Article Title: Species-specific inflammatory responses of chondrocytes: Toward evidence-based model selection in OA research

    Journal: iScience

    doi: 10.1016/j.isci.2026.117710


    Figure Legend Snippet:

    Techniques Used: Recombinant, Proliferation Assay, Qubit, RNA Sequencing, Software, Analysis

    Related Articles

    Titration:

    Article Title: Leishmania and phlebovirus seroprevalence in dogs in two non-endemic central European countries: Austria and Germany
    Article Snippet: included TCID 50 assay for viral titration confirmation. After 5 days for TOSV and 6 days for SFSV, photos of each well of the 96-well microplates were taken by using Incucyte SX5 Live-Cell Analysis (Sartorius, Göttingen, Germany) and results were analyzed to determine cytopathic effect (CPE) and neutralization titers. A sensitivity of 98.1% and specificity of 98.8% is calculated for CPE-based vir

    Sensitivity:

    Article Title: Leishmania and phlebovirus seroprevalence in dogs in two non-endemic central European countries: Austria and Germany
    Article Snippet: included TCID 50 assay for viral titration confirmation. After 5 days for TOSV and 6 days for SFSV, photos of each well of the 96-well microplates were taken by using Incucyte SX5 Live-Cell Analysis (Sartorius, Göttingen, Germany) and results were analyzed to determine cytopathic effect (CPE) and neutralization titers. A sensitivity of 98.1% and specificity of 98.8% is calculated for CPE-based vir

    Virus:

    Article Title: Leishmania and phlebovirus seroprevalence in dogs in two non-endemic central European countries: Austria and Germany
    Article Snippet: included TCID 50 assay for viral titration confirmation. After 5 days for TOSV and 6 days for SFSV, photos of each well of the 96-well microplates were taken by using Incucyte SX5 Live-Cell Analysis (Sartorius, Göttingen, Germany) and results were analyzed to determine cytopathic effect (CPE) and neutralization titers. A sensitivity of 98.1% and specificity of 98.8% is calculated for CPE-based vir

    Analysis:

    Article Title: Leishmania and phlebovirus seroprevalence in dogs in two non-endemic central European countries: Austria and Germany
    Article Snippet: included TCID 50 assay for viral titration confirmation. After 5 days for TOSV and 6 days for SFSV, photos of each well of the 96-well microplates were taken by using Incucyte SX5 Live-Cell Analysis (Sartorius, Göttingen, Germany) and results were analyzed to determine cytopathic effect (CPE) and neutralization titers. A sensitivity of 98.1% and specificity of 98.8% is calculated for CPE-based vir

    Neutralization:

    Article Title: Leishmania and phlebovirus seroprevalence in dogs in two non-endemic central European countries: Austria and Germany
    Article Snippet: included TCID 50 assay for viral titration confirmation. After 5 days for TOSV and 6 days for SFSV, photos of each well of the 96-well microplates were taken by using Incucyte SX5 Live-Cell Analysis (Sartorius, Göttingen, Germany) and results were analyzed to determine cytopathic effect (CPE) and neutralization titers. A sensitivity of 98.1% and specificity of 98.8% is calculated for CPE-based vir

    Software:

    Article Title: Leishmania and phlebovirus seroprevalence in dogs in two non-endemic central European countries: Austria and Germany
    Article Snippet: included TCID 50 assay for viral titration confirmation. After 5 days for TOSV and 6 days for SFSV, photos of each well of the 96-well microplates were taken by using Incucyte SX5 Live-Cell Analysis (Sartorius, Göttingen, Germany) and results were analyzed to determine cytopathic effect (CPE) and neutralization titers. A sensitivity of 98.1% and specificity of 98.8% is calculated for CPE-based vir

    Concentration Assay:

    Article Title: Leishmania and phlebovirus seroprevalence in dogs in two non-endemic central European countries: Austria and Germany
    Article Snippet: included TCID 50 assay for viral titration confirmation. After 5 days for TOSV and 6 days for SFSV, photos of each well of the 96-well microplates were taken by using Incucyte SX5 Live-Cell Analysis (Sartorius, Göttingen, Germany) and results were analyzed to determine cytopathic effect (CPE) and neutralization titers. A sensitivity of 98.1% and specificity of 98.8% is calculated for CPE-based vir

    Staining:

    Article Title: Leishmania and phlebovirus seroprevalence in dogs in two non-endemic central European countries: Austria and Germany
    Article Snippet: included TCID 50 assay for viral titration confirmation. After 5 days for TOSV and 6 days for SFSV, photos of each well of the 96-well microplates were taken by using Incucyte SX5 Live-Cell Analysis (Sartorius, Göttingen, Germany) and results were analyzed to determine cytopathic effect (CPE) and neutralization titers. A sensitivity of 98.1% and specificity of 98.8% is calculated for CPE-based vir

    Oligomer Restriction:

    Article Title: Leishmania and phlebovirus seroprevalence in dogs in two non-endemic central European countries: Austria and Germany
    Article Snippet: included TCID 50 assay for viral titration confirmation. After 5 days for TOSV and 6 days for SFSV, photos of each well of the 96-well microplates were taken by using Incucyte SX5 Live-Cell Analysis (Sartorius, Göttingen, Germany) and results were analyzed to determine cytopathic effect (CPE) and neutralization titers. A sensitivity of 98.1% and specificity of 98.8% is calculated for CPE-based vir

    Infection:

    Article Title: Leishmania and phlebovirus seroprevalence in dogs in two non-endemic central European countries: Austria and Germany
    Article Snippet: included TCID 50 assay for viral titration confirmation. After 5 days for TOSV and 6 days for SFSV, photos of each well of the 96-well microplates were taken by using Incucyte SX5 Live-Cell Analysis (Sartorius, Göttingen, Germany) and results were analyzed to determine cytopathic effect (CPE) and neutralization titers. A sensitivity of 98.1% and specificity of 98.8% is calculated for CPE-based vir

    Live Cell Imaging:

    Article Title: Leishmania and phlebovirus seroprevalence in dogs in two non-endemic central European countries: Austria and Germany
    Article Snippet: included TCID 50 assay for viral titration confirmation. After 5 days for TOSV and 6 days for SFSV, photos of each well of the 96-well microplates were taken by using Incucyte SX5 Live-Cell Analysis (Sartorius, Göttingen, Germany) and results were analyzed to determine cytopathic effect (CPE) and neutralization titers. A sensitivity of 98.1% and specificity of 98.8% is calculated for CPE-based vir

    Imaging:

    Article Title: Leishmania and phlebovirus seroprevalence in dogs in two non-endemic central European countries: Austria and Germany
    Article Snippet: included TCID 50 assay for viral titration confirmation. After 5 days for TOSV and 6 days for SFSV, photos of each well of the 96-well microplates were taken by using Incucyte SX5 Live-Cell Analysis (Sartorius, Göttingen, Germany) and results were analyzed to determine cytopathic effect (CPE) and neutralization titers. A sensitivity of 98.1% and specificity of 98.8% is calculated for CPE-based vir

    Incubation:

    Article Title: Leishmania and phlebovirus seroprevalence in dogs in two non-endemic central European countries: Austria and Germany
    Article Snippet: included TCID 50 assay for viral titration confirmation. After 5 days for TOSV and 6 days for SFSV, photos of each well of the 96-well microplates were taken by using Incucyte SX5 Live-Cell Analysis (Sartorius, Göttingen, Germany) and results were analyzed to determine cytopathic effect (CPE) and neutralization titers. A sensitivity of 98.1% and specificity of 98.8% is calculated for CPE-based vir

    Fluorescence:

    Article Title: Leishmania and phlebovirus seroprevalence in dogs in two non-endemic central European countries: Austria and Germany
    Article Snippet: included TCID 50 assay for viral titration confirmation. After 5 days for TOSV and 6 days for SFSV, photos of each well of the 96-well microplates were taken by using Incucyte SX5 Live-Cell Analysis (Sartorius, Göttingen, Germany) and results were analyzed to determine cytopathic effect (CPE) and neutralization titers. A sensitivity of 98.1% and specificity of 98.8% is calculated for CPE-based vir



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    Image Search Results


    Journal: iScience

    Article Title: Species-specific inflammatory responses of chondrocytes: Toward evidence-based model selection in OA research

    doi: 10.1016/j.isci.2026.117710

    Figure Lengend Snippet:

    Article Snippet: IncuCyte software analysis , Sartorius , RRID:SCR_003935; https://www.sartorius.com/en/product.

    Techniques: Recombinant, Proliferation Assay, Qubit, RNA Sequencing, Software, Analysis

    (A) DND1 (purple) and NANOS3 (pink) residues interacting with the N3-DRE. Filled shading, residues substituted with alanine for functional analysis. (B) DND1–NANOS3 co-expression constructs with indicated mutations (top) or truncations (bottom). (C) Schematic of assays performed with cells expressing constructs from (B). (D) Assay results for DND1–NANOS3 constructs with DND1 point mutants: ( 1 ) IncuCyte growth assays; ( 2 ) expression of N3-DRE-containing RNAs; ( 3 ) protein levels of N3-DRE-containing targets (CDK1, EHMT2, and CNOT6; immunoblots in Fig. S5 ). (E) As in (D), with NANOS3 point mutations. (F) DND1 K196A loses selectivity for the N3-DRE G3 nucleotide in vitro . Error bars, K d confidence interval from MST data fitting. (G) As in (D), with DND1 or NANOS3 truncations. (H) Effects of DND1/NANOS3 mutations or deletions on RNA turnover. Left, median fold changes in k deg for each N3-DRE class, normalized to the corresponding No motif group. Middle, median fold changes in k syn . Right, median fold changes in transcript half-life. Corresponding violin plots and CDFs are shown in Figures S5F and S5G . (I) Summary of the functional impact of RNA-binding residue mutations and IDR deletion. Statistics (D-F): Cell growth: Scale bar, 400 μm (bottom right image only). CDFs: n, number of genes; ML, median log 2 -fold change; δ, Cliff’s delta; p , two-sided Wilcoxon rank-sum test. Protein quantification: Error bars indicate S.D. Two-sided Student’s t -test ( n = 3 independent experiments). Exact p -values are provided in Source Data. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001. See also Figure S5 and Table S1 .

    Journal: Molecular cell

    Article Title: DND1–NANOS3 shapes the PGC transcriptome via a heptanucleotide sequence in mRNA 3′-UTRs

    doi: 10.1016/j.molcel.2026.09.010

    Figure Lengend Snippet: (A) DND1 (purple) and NANOS3 (pink) residues interacting with the N3-DRE. Filled shading, residues substituted with alanine for functional analysis. (B) DND1–NANOS3 co-expression constructs with indicated mutations (top) or truncations (bottom). (C) Schematic of assays performed with cells expressing constructs from (B). (D) Assay results for DND1–NANOS3 constructs with DND1 point mutants: ( 1 ) IncuCyte growth assays; ( 2 ) expression of N3-DRE-containing RNAs; ( 3 ) protein levels of N3-DRE-containing targets (CDK1, EHMT2, and CNOT6; immunoblots in Fig. S5 ). (E) As in (D), with NANOS3 point mutations. (F) DND1 K196A loses selectivity for the N3-DRE G3 nucleotide in vitro . Error bars, K d confidence interval from MST data fitting. (G) As in (D), with DND1 or NANOS3 truncations. (H) Effects of DND1/NANOS3 mutations or deletions on RNA turnover. Left, median fold changes in k deg for each N3-DRE class, normalized to the corresponding No motif group. Middle, median fold changes in k syn . Right, median fold changes in transcript half-life. Corresponding violin plots and CDFs are shown in Figures S5F and S5G . (I) Summary of the functional impact of RNA-binding residue mutations and IDR deletion. Statistics (D-F): Cell growth: Scale bar, 400 μm (bottom right image only). CDFs: n, number of genes; ML, median log 2 -fold change; δ, Cliff’s delta; p , two-sided Wilcoxon rank-sum test. Protein quantification: Error bars indicate S.D. Two-sided Student’s t -test ( n = 3 independent experiments). Exact p -values are provided in Source Data. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001. See also Figure S5 and Table S1 .

    Article Snippet: Cell proliferation was monitored using the IncuCyte S3 Live-Cell Analysis System (Sartorius) by measuring confluence over time.

    Techniques: RNA Binding Assay, Functional Assay, Analysis, Expressing, Construct, Western Blot, In Vitro, Residue