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macro cell count analysis software  (KEYENCE)

 
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    KEYENCE macro cell count analysis software
    Macro Cell Count Analysis Software, supplied by KEYENCE, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/macro+cell-count+software/macro+cell+count+analysis+software/pmc12209159-122-2-1
    Average 90 stars, based on 1 article reviews
    macro cell count analysis software - by Bioz Stars, 2026-08
    90/100 stars

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    macro cell count analysis software  (KEYENCE)
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    Macro Cell Count Analysis Software, supplied by KEYENCE, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/macro+cell-count+software/macro+cell+count+analysis+software/pmc12209159-122-2-1
    Average 90 stars, based on 1 article reviews
    macro cell count analysis software - by Bioz Stars, 2026-08
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    macro cell counting software  (KEYENCE)
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    ( A-C ) HEC-1-A cells were transfected with Xenopus β-catenin ΔEX3 and NT (non-targeting) or NT5E siRNA and cultured in 1% O 2 and 5% CO 2 for 48 hours. (A) Representative immunofluorescence images used in quantifying nuclear localization of myc-β-catenin ΔEX3 . Scale bar: 50 µm. Fluorescence intensity was determined with BZ-X800 Analyzer <t>Macro</t> <t>cell</t> count <t>software</t> (Keyence). ( B) Validation of CD73 knockdown and ( C ) nuclear fluorescence intensity of myc-β-catenin ΔEX3 . ( D-F ) Representative immunoblots of n = 2 independent experiments of cellular fractionations from NT5E WT and NT5E KO HEC-1-A cells. Cells were transfected with ( D ) Xenopus β-catenin ΔEX3 or patient-specific β-catenin mutants (E) S37F or (F) G34R. Graphs show densitometry for myc-β-catenin mutant expression for each cellular fraction normalized to myc-β-catenin mutant expression in the whole cell lysate (WCL). Cellular fraction markers: Rab11a (membrane), SP1 (nuclear), and H2AX (chromatin). ( G ) mRNA and ( H ) protein expression of differentially expressed cell-cell adhesion components in NT5E WT and NT5E KO HEC-1-A cells. Data represent the mean ± SEM. ****P < 0.0001, Mann-Whitney test; **P < 0.01, ***P < 0.005; Welch t-test.
    Macro Cell Counting Software, supplied by KEYENCE, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ( A-C ) HEC-1-A cells were transfected with Xenopus β-catenin ΔEX3 and NT (non-targeting) or NT5E siRNA and cultured in 1% O 2 and 5% CO 2 for 48 hours. (A) Representative immunofluorescence images used in quantifying nuclear localization of myc-β-catenin ΔEX3 . Scale bar: 50 µm. Fluorescence intensity was determined with BZ-X800 Analyzer <t>Macro</t> <t>cell</t> count <t>software</t> (Keyence). ( B) Validation of CD73 knockdown and ( C ) nuclear fluorescence intensity of myc-β-catenin ΔEX3 . ( D-F ) Representative immunoblots of n = 2 independent experiments of cellular fractionations from NT5E WT and NT5E KO HEC-1-A cells. Cells were transfected with ( D ) Xenopus β-catenin ΔEX3 or patient-specific β-catenin mutants (E) S37F or (F) G34R. Graphs show densitometry for myc-β-catenin mutant expression for each cellular fraction normalized to myc-β-catenin mutant expression in the whole cell lysate (WCL). Cellular fraction markers: Rab11a (membrane), SP1 (nuclear), and H2AX (chromatin). ( G ) mRNA and ( H ) protein expression of differentially expressed cell-cell adhesion components in NT5E WT and NT5E KO HEC-1-A cells. Data represent the mean ± SEM. ****P < 0.0001, Mann-Whitney test; **P < 0.01, ***P < 0.005; Welch t-test.
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    ( A-C ) HEC-1-A cells were transfected with Xenopus β-catenin ΔEX3 and NT (non-targeting) or NT5E siRNA and cultured in 1% O 2 and 5% CO 2 for 48 hours. (A) Representative immunofluorescence images used in quantifying nuclear localization of myc-β-catenin ΔEX3 . Scale bar: 50 µm. Fluorescence intensity was determined with BZ-X800 Analyzer <t>Macro</t> <t>cell</t> count <t>software</t> (Keyence). ( B) Validation of CD73 knockdown and ( C ) nuclear fluorescence intensity of myc-β-catenin ΔEX3 . ( D-F ) Representative immunoblots of n = 2 independent experiments of cellular fractionations from NT5E WT and NT5E KO HEC-1-A cells. Cells were transfected with ( D ) Xenopus β-catenin ΔEX3 or patient-specific β-catenin mutants (E) S37F or (F) G34R. Graphs show densitometry for myc-β-catenin mutant expression for each cellular fraction normalized to myc-β-catenin mutant expression in the whole cell lysate (WCL). Cellular fraction markers: Rab11a (membrane), SP1 (nuclear), and H2AX (chromatin). ( G ) mRNA and ( H ) protein expression of differentially expressed cell-cell adhesion components in NT5E WT and NT5E KO HEC-1-A cells. Data represent the mean ± SEM. ****P < 0.0001, Mann-Whitney test; **P < 0.01, ***P < 0.005; Welch t-test.
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    ( A-C ) HEC-1-A cells were transfected with Xenopus β-catenin ΔEX3 and NT (non-targeting) or NT5E siRNA and cultured in 1% O 2 and 5% CO 2 for 48 hours. (A) Representative immunofluorescence images used in quantifying nuclear localization of myc-β-catenin ΔEX3 . Scale bar: 50 µm. Fluorescence intensity was determined with BZ-X800 Analyzer <t>Macro</t> <t>cell</t> count <t>software</t> (Keyence). ( B) Validation of CD73 knockdown and ( C ) nuclear fluorescence intensity of myc-β-catenin ΔEX3 . ( D-F ) Representative immunoblots of n = 2 independent experiments of cellular fractionations from NT5E WT and NT5E KO HEC-1-A cells. Cells were transfected with ( D ) Xenopus β-catenin ΔEX3 or patient-specific β-catenin mutants (E) S37F or (F) G34R. Graphs show densitometry for myc-β-catenin mutant expression for each cellular fraction normalized to myc-β-catenin mutant expression in the whole cell lysate (WCL). Cellular fraction markers: Rab11a (membrane), SP1 (nuclear), and H2AX (chromatin). ( G ) mRNA and ( H ) protein expression of differentially expressed cell-cell adhesion components in NT5E WT and NT5E KO HEC-1-A cells. Data represent the mean ± SEM. ****P < 0.0001, Mann-Whitney test; **P < 0.01, ***P < 0.005; Welch t-test.
    Macro Cell Count Software, supplied by KEYENCE, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ( A-C ) HEC-1-A cells were transfected with Xenopus β-catenin ΔEX3 and NT (non-targeting) or NT5E siRNA and cultured in 1% O 2 and 5% CO 2 for 48 hours. (A) Representative immunofluorescence images used in quantifying nuclear localization of myc-β-catenin ΔEX3 . Scale bar: 50 µm. Fluorescence intensity was determined with BZ-X800 Analyzer <t>Macro</t> <t>cell</t> count <t>software</t> (Keyence). ( B) Validation of CD73 knockdown and ( C ) nuclear fluorescence intensity of myc-β-catenin ΔEX3 . ( D-F ) Representative immunoblots of n = 2 independent experiments of cellular fractionations from NT5E WT and NT5E KO HEC-1-A cells. Cells were transfected with ( D ) Xenopus β-catenin ΔEX3 or patient-specific β-catenin mutants (E) S37F or (F) G34R. Graphs show densitometry for myc-β-catenin mutant expression for each cellular fraction normalized to myc-β-catenin mutant expression in the whole cell lysate (WCL). Cellular fraction markers: Rab11a (membrane), SP1 (nuclear), and H2AX (chromatin). ( G ) mRNA and ( H ) protein expression of differentially expressed cell-cell adhesion components in NT5E WT and NT5E KO HEC-1-A cells. Data represent the mean ± SEM. ****P < 0.0001, Mann-Whitney test; **P < 0.01, ***P < 0.005; Welch t-test.
    Measurement Software Program Hybrid Cell Count And Macro Cell Count, supplied by KEYENCE, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Average 90 stars, based on 1 article reviews
    measurement software program hybrid cell count and macro cell count - by Bioz Stars, 2026-08
    90/100 stars
    		  Buy from Supplier
    macro cell count software  (KEYENCE)
    90
    KEYENCE macro cell count software
    ( A-C ) HEC-1-A cells were transfected with Xenopus β-catenin ΔEX3 and NT (non-targeting) or NT5E siRNA and cultured in 1% O 2 and 5% CO 2 for 48 hours. (A) Representative immunofluorescence images used in quantifying nuclear localization of myc-β-catenin ΔEX3 . Scale bar: 50 µm. Fluorescence intensity was determined with BZ-X800 Analyzer <t>Macro</t> <t>cell</t> count <t>software</t> (Keyence). ( B) Validation of CD73 knockdown and ( C ) nuclear fluorescence intensity of myc-β-catenin ΔEX3 . ( D-F ) Representative immunoblots of n = 2 independent experiments of cellular fractionations from NT5E WT and NT5E KO HEC-1-A cells. Cells were transfected with ( D ) Xenopus β-catenin ΔEX3 or patient-specific β-catenin mutants (E) S37F or (F) G34R. Graphs show densitometry for myc-β-catenin mutant expression for each cellular fraction normalized to myc-β-catenin mutant expression in the whole cell lysate (WCL). Cellular fraction markers: Rab11a (membrane), SP1 (nuclear), and H2AX (chromatin). ( G ) mRNA and ( H ) protein expression of differentially expressed cell-cell adhesion components in NT5E WT and NT5E KO HEC-1-A cells. Data represent the mean ± SEM. ****P < 0.0001, Mann-Whitney test; **P < 0.01, ***P < 0.005; Welch t-test.
    Macro Cell Count Software, supplied by KEYENCE, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/macro+cell-count+software/macro+cell+count+analysis+software/pm32694970-156-13-22
    Average 90 stars, based on 1 article reviews
    macro cell count software - by Bioz Stars, 2026-08
    90/100 stars
    		  Buy from Supplier
    measurement software programs hybrid cell count and macro cell count  (KEYENCE)
    90
    KEYENCE measurement software programs hybrid cell count and macro cell count
    ( A-C ) HEC-1-A cells were transfected with Xenopus β-catenin ΔEX3 and NT (non-targeting) or NT5E siRNA and cultured in 1% O 2 and 5% CO 2 for 48 hours. (A) Representative immunofluorescence images used in quantifying nuclear localization of myc-β-catenin ΔEX3 . Scale bar: 50 µm. Fluorescence intensity was determined with BZ-X800 Analyzer <t>Macro</t> <t>cell</t> count <t>software</t> (Keyence). ( B) Validation of CD73 knockdown and ( C ) nuclear fluorescence intensity of myc-β-catenin ΔEX3 . ( D-F ) Representative immunoblots of n = 2 independent experiments of cellular fractionations from NT5E WT and NT5E KO HEC-1-A cells. Cells were transfected with ( D ) Xenopus β-catenin ΔEX3 or patient-specific β-catenin mutants (E) S37F or (F) G34R. Graphs show densitometry for myc-β-catenin mutant expression for each cellular fraction normalized to myc-β-catenin mutant expression in the whole cell lysate (WCL). Cellular fraction markers: Rab11a (membrane), SP1 (nuclear), and H2AX (chromatin). ( G ) mRNA and ( H ) protein expression of differentially expressed cell-cell adhesion components in NT5E WT and NT5E KO HEC-1-A cells. Data represent the mean ± SEM. ****P < 0.0001, Mann-Whitney test; **P < 0.01, ***P < 0.005; Welch t-test.
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    Average 90 stars, based on 1 article reviews
    measurement software programs hybrid cell count and macro cell count - by Bioz Stars, 2026-08
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    bz-9000 analyser macro cell count software  (KEYENCE)
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    ( A-C ) HEC-1-A cells were transfected with Xenopus β-catenin ΔEX3 and NT (non-targeting) or NT5E siRNA and cultured in 1% O 2 and 5% CO 2 for 48 hours. (A) Representative immunofluorescence images used in quantifying nuclear localization of myc-β-catenin ΔEX3 . Scale bar: 50 µm. Fluorescence intensity was determined with BZ-X800 Analyzer <t>Macro</t> <t>cell</t> count <t>software</t> (Keyence). ( B) Validation of CD73 knockdown and ( C ) nuclear fluorescence intensity of myc-β-catenin ΔEX3 . ( D-F ) Representative immunoblots of n = 2 independent experiments of cellular fractionations from NT5E WT and NT5E KO HEC-1-A cells. Cells were transfected with ( D ) Xenopus β-catenin ΔEX3 or patient-specific β-catenin mutants (E) S37F or (F) G34R. Graphs show densitometry for myc-β-catenin mutant expression for each cellular fraction normalized to myc-β-catenin mutant expression in the whole cell lysate (WCL). Cellular fraction markers: Rab11a (membrane), SP1 (nuclear), and H2AX (chromatin). ( G ) mRNA and ( H ) protein expression of differentially expressed cell-cell adhesion components in NT5E WT and NT5E KO HEC-1-A cells. Data represent the mean ± SEM. ****P < 0.0001, Mann-Whitney test; **P < 0.01, ***P < 0.005; Welch t-test.
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    Image Search Results


    ( A-C ) HEC-1-A cells were transfected with Xenopus β-catenin ΔEX3 and NT (non-targeting) or NT5E siRNA and cultured in 1% O 2 and 5% CO 2 for 48 hours. (A) Representative immunofluorescence images used in quantifying nuclear localization of myc-β-catenin ΔEX3 . Scale bar: 50 µm. Fluorescence intensity was determined with BZ-X800 Analyzer Macro cell count software (Keyence). ( B) Validation of CD73 knockdown and ( C ) nuclear fluorescence intensity of myc-β-catenin ΔEX3 . ( D-F ) Representative immunoblots of n = 2 independent experiments of cellular fractionations from NT5E WT and NT5E KO HEC-1-A cells. Cells were transfected with ( D ) Xenopus β-catenin ΔEX3 or patient-specific β-catenin mutants (E) S37F or (F) G34R. Graphs show densitometry for myc-β-catenin mutant expression for each cellular fraction normalized to myc-β-catenin mutant expression in the whole cell lysate (WCL). Cellular fraction markers: Rab11a (membrane), SP1 (nuclear), and H2AX (chromatin). ( G ) mRNA and ( H ) protein expression of differentially expressed cell-cell adhesion components in NT5E WT and NT5E KO HEC-1-A cells. Data represent the mean ± SEM. ****P < 0.0001, Mann-Whitney test; **P < 0.01, ***P < 0.005; Welch t-test.

    Journal: bioRxiv

    Article Title: CD73 restrains mutant β-catenin oncogenic activity in endometrial carcinomas

    doi: 10.1101/2024.11.18.624183

    Figure Lengend Snippet: ( A-C ) HEC-1-A cells were transfected with Xenopus β-catenin ΔEX3 and NT (non-targeting) or NT5E siRNA and cultured in 1% O 2 and 5% CO 2 for 48 hours. (A) Representative immunofluorescence images used in quantifying nuclear localization of myc-β-catenin ΔEX3 . Scale bar: 50 µm. Fluorescence intensity was determined with BZ-X800 Analyzer Macro cell count software (Keyence). ( B) Validation of CD73 knockdown and ( C ) nuclear fluorescence intensity of myc-β-catenin ΔEX3 . ( D-F ) Representative immunoblots of n = 2 independent experiments of cellular fractionations from NT5E WT and NT5E KO HEC-1-A cells. Cells were transfected with ( D ) Xenopus β-catenin ΔEX3 or patient-specific β-catenin mutants (E) S37F or (F) G34R. Graphs show densitometry for myc-β-catenin mutant expression for each cellular fraction normalized to myc-β-catenin mutant expression in the whole cell lysate (WCL). Cellular fraction markers: Rab11a (membrane), SP1 (nuclear), and H2AX (chromatin). ( G ) mRNA and ( H ) protein expression of differentially expressed cell-cell adhesion components in NT5E WT and NT5E KO HEC-1-A cells. Data represent the mean ± SEM. ****P < 0.0001, Mann-Whitney test; **P < 0.01, ***P < 0.005; Welch t-test.

    Article Snippet: Relative intensity for each image was measured using Keyence macro cell counting software.

    Techniques: Transfection, Cell Culture, Immunofluorescence, Fluorescence, Cell Counting, Software, Knockdown, Western Blot, Mutagenesis, Expressing, Membrane, MANN-WHITNEY