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heidelberg engineering inbuilt image processing software
Inbuilt Image Processing Software, supplied by heidelberg engineering, 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/inbuilt+software/inbuilt+image+processing+software/pm29490343-79-7-14
Average 90 stars, based on 1 article reviews
inbuilt image processing software - by Bioz Stars, 2026-09
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Article Title: Sampling the Visual Field Based on Individual Retinal Nerve Fiber Layer Thickness Profile.
Article Snippet: .. Downloaded From: https://iovs.arvojournals.org/ on 08/06/2018 The inbuilt image processing software of the OCT device (Heidelberg Engineering GmBH) was used to segment the RNFL thickness and this was subsequently manually crosschecked and corrected where necessary by one of the authors (SBG). ..



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Effects of structurally different arsenicals on apoptotic cell death. ( A ) TUNEL assay of skin sections from vehicle- or treated mice revealed abundant TUNEL-positive (green) cells in DPCA and DPCYA-treated skin, indicating robust cell death (Yellow arrows) at 24 and 72 h. Scale bar-50 µm. ( B ) Histogram showing quantitative analysis of TUNEL-positive green cells. Keyence <t>Microscope</t> inbuilt software (Model <t>BZ-X710,</t> KEYENCE, Osaka, Japan) was used for quantitative analysis of TUNEL-positive cells. Multiple microphotographs captured at 10X magnification was used for quantitative analysis. ( C ) Western blot analysis shows augmented expression of cleaved caspase 3 in arsenical-challenged mice. β-actin was used as an endogenous control. (D) Histogram representing densitometry analysis of western blots band intensity. (Also see supplementary fig. S4, S5 and S6 for full images of immunoblots). *P < 0.05, **P < 0.01,***P < 0.001, ****P < 0.0001 showing significance compared to vehicle treated controls. ns, non-significant. N = 3/group.
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Effects of structurally different arsenicals on apoptotic cell death. ( A ) TUNEL assay of skin sections from vehicle- or treated mice revealed abundant TUNEL-positive (green) cells in DPCA and DPCYA-treated skin, indicating robust cell death (Yellow arrows) at 24 and 72 h. Scale bar-50 µm. ( B ) Histogram showing quantitative analysis of TUNEL-positive green cells. Keyence <t>Microscope</t> inbuilt software (Model <t>BZ-X710,</t> KEYENCE, Osaka, Japan) was used for quantitative analysis of TUNEL-positive cells. Multiple microphotographs captured at 10X magnification was used for quantitative analysis. ( C ) Western blot analysis shows augmented expression of cleaved caspase 3 in arsenical-challenged mice. β-actin was used as an endogenous control. (D) Histogram representing densitometry analysis of western blots band intensity. (Also see supplementary fig. S4, S5 and S6 for full images of immunoblots). *P < 0.05, **P < 0.01,***P < 0.001, ****P < 0.0001 showing significance compared to vehicle treated controls. ns, non-significant. N = 3/group.
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Effects of structurally different arsenicals on apoptotic cell death. ( A ) TUNEL assay of skin sections from vehicle- or treated mice revealed abundant TUNEL-positive (green) cells in DPCA and DPCYA-treated skin, indicating robust cell death (Yellow arrows) at 24 and 72 h. Scale bar-50 µm. ( B ) Histogram showing quantitative analysis of TUNEL-positive green cells. Keyence <t>Microscope</t> inbuilt software (Model <t>BZ-X710,</t> KEYENCE, Osaka, Japan) was used for quantitative analysis of TUNEL-positive cells. Multiple microphotographs captured at 10X magnification was used for quantitative analysis. ( C ) Western blot analysis shows augmented expression of cleaved caspase 3 in arsenical-challenged mice. β-actin was used as an endogenous control. (D) Histogram representing densitometry analysis of western blots band intensity. (Also see supplementary fig. S4, S5 and S6 for full images of immunoblots). *P < 0.05, **P < 0.01,***P < 0.001, ****P < 0.0001 showing significance compared to vehicle treated controls. ns, non-significant. N = 3/group.
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Effects of structurally different arsenicals on apoptotic cell death. ( A ) TUNEL assay of skin sections from vehicle- or treated mice revealed abundant TUNEL-positive (green) cells in DPCA and DPCYA-treated skin, indicating robust cell death (Yellow arrows) at 24 and 72 h. Scale bar-50 µm. ( B ) Histogram showing quantitative analysis of TUNEL-positive green cells. Keyence <t>Microscope</t> inbuilt software (Model <t>BZ-X710,</t> KEYENCE, Osaka, Japan) was used for quantitative analysis of TUNEL-positive cells. Multiple microphotographs captured at 10X magnification was used for quantitative analysis. ( C ) Western blot analysis shows augmented expression of cleaved caspase 3 in arsenical-challenged mice. β-actin was used as an endogenous control. (D) Histogram representing densitometry analysis of western blots band intensity. (Also see supplementary fig. S4, S5 and S6 for full images of immunoblots). *P < 0.05, **P < 0.01,***P < 0.001, ****P < 0.0001 showing significance compared to vehicle treated controls. ns, non-significant. N = 3/group.
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Effects of structurally different arsenicals on apoptotic cell death. ( A ) TUNEL assay of skin sections from vehicle- or treated mice revealed abundant TUNEL-positive (green) cells in DPCA and DPCYA-treated skin, indicating robust cell death (Yellow arrows) at 24 and 72 h. Scale bar-50 µm. ( B ) Histogram showing quantitative analysis of TUNEL-positive green cells. Keyence <t>Microscope</t> inbuilt software (Model <t>BZ-X710,</t> KEYENCE, Osaka, Japan) was used for quantitative analysis of TUNEL-positive cells. Multiple microphotographs captured at 10X magnification was used for quantitative analysis. ( C ) Western blot analysis shows augmented expression of cleaved caspase 3 in arsenical-challenged mice. β-actin was used as an endogenous control. (D) Histogram representing densitometry analysis of western blots band intensity. (Also see supplementary fig. S4, S5 and S6 for full images of immunoblots). *P < 0.05, **P < 0.01,***P < 0.001, ****P < 0.0001 showing significance compared to vehicle treated controls. ns, non-significant. N = 3/group.
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Effects of structurally different arsenicals on apoptotic cell death. ( A ) TUNEL assay of skin sections from vehicle- or treated mice revealed abundant TUNEL-positive (green) cells in DPCA and DPCYA-treated skin, indicating robust cell death (Yellow arrows) at 24 and 72 h. Scale bar-50 µm. ( B ) Histogram showing quantitative analysis of TUNEL-positive green cells. Keyence <t>Microscope</t> inbuilt software (Model <t>BZ-X710,</t> KEYENCE, Osaka, Japan) was used for quantitative analysis of TUNEL-positive cells. Multiple microphotographs captured at 10X magnification was used for quantitative analysis. ( C ) Western blot analysis shows augmented expression of cleaved caspase 3 in arsenical-challenged mice. β-actin was used as an endogenous control. (D) Histogram representing densitometry analysis of western blots band intensity. (Also see supplementary fig. S4, S5 and S6 for full images of immunoblots). *P < 0.05, **P < 0.01,***P < 0.001, ****P < 0.0001 showing significance compared to vehicle treated controls. ns, non-significant. N = 3/group.
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Effects of structurally different arsenicals on apoptotic cell death. ( A ) TUNEL assay of skin sections from vehicle- or treated mice revealed abundant TUNEL-positive (green) cells in DPCA and DPCYA-treated skin, indicating robust cell death (Yellow arrows) at 24 and 72 h. Scale bar-50 µm. ( B ) Histogram showing quantitative analysis of TUNEL-positive green cells. Keyence <t>Microscope</t> inbuilt software (Model <t>BZ-X710,</t> KEYENCE, Osaka, Japan) was used for quantitative analysis of TUNEL-positive cells. Multiple microphotographs captured at 10X magnification was used for quantitative analysis. ( C ) Western blot analysis shows augmented expression of cleaved caspase 3 in arsenical-challenged mice. β-actin was used as an endogenous control. (D) Histogram representing densitometry analysis of western blots band intensity. (Also see supplementary fig. S4, S5 and S6 for full images of immunoblots). *P < 0.05, **P < 0.01,***P < 0.001, ****P < 0.0001 showing significance compared to vehicle treated controls. ns, non-significant. N = 3/group.
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Effects of structurally different arsenicals on apoptotic cell death. ( A ) TUNEL assay of skin sections from vehicle- or treated mice revealed abundant TUNEL-positive (green) cells in DPCA and DPCYA-treated skin, indicating robust cell death (Yellow arrows) at 24 and 72 h. Scale bar-50 µm. ( B ) Histogram showing quantitative analysis of TUNEL-positive green cells. Keyence <t>Microscope</t> inbuilt software (Model <t>BZ-X710,</t> KEYENCE, Osaka, Japan) was used for quantitative analysis of TUNEL-positive cells. Multiple microphotographs captured at 10X magnification was used for quantitative analysis. ( C ) Western blot analysis shows augmented expression of cleaved caspase 3 in arsenical-challenged mice. β-actin was used as an endogenous control. (D) Histogram representing densitometry analysis of western blots band intensity. (Also see supplementary fig. S4, S5 and S6 for full images of immunoblots). *P < 0.05, **P < 0.01,***P < 0.001, ****P < 0.0001 showing significance compared to vehicle treated controls. ns, non-significant. N = 3/group.
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Effects of structurally different arsenicals on apoptotic cell death. ( A ) TUNEL assay of skin sections from vehicle- or treated mice revealed abundant TUNEL-positive (green) cells in DPCA and DPCYA-treated skin, indicating robust cell death (Yellow arrows) at 24 and 72 h. Scale bar-50 µm. ( B ) Histogram showing quantitative analysis of TUNEL-positive green cells. Keyence Microscope inbuilt software (Model BZ-X710, KEYENCE, Osaka, Japan) was used for quantitative analysis of TUNEL-positive cells. Multiple microphotographs captured at 10X magnification was used for quantitative analysis. ( C ) Western blot analysis shows augmented expression of cleaved caspase 3 in arsenical-challenged mice. β-actin was used as an endogenous control. (D) Histogram representing densitometry analysis of western blots band intensity. (Also see supplementary fig. S4, S5 and S6 for full images of immunoblots). *P < 0.05, **P < 0.01,***P < 0.001, ****P < 0.0001 showing significance compared to vehicle treated controls. ns, non-significant. N = 3/group.

Journal: Scientific Reports

Article Title: Common molecular profile of multiple structurally distinct warfare arsenicals in causing cutaneous chemical vesicant injury

doi: 10.1038/s41598-024-83513-1

Figure Lengend Snippet: Effects of structurally different arsenicals on apoptotic cell death. ( A ) TUNEL assay of skin sections from vehicle- or treated mice revealed abundant TUNEL-positive (green) cells in DPCA and DPCYA-treated skin, indicating robust cell death (Yellow arrows) at 24 and 72 h. Scale bar-50 µm. ( B ) Histogram showing quantitative analysis of TUNEL-positive green cells. Keyence Microscope inbuilt software (Model BZ-X710, KEYENCE, Osaka, Japan) was used for quantitative analysis of TUNEL-positive cells. Multiple microphotographs captured at 10X magnification was used for quantitative analysis. ( C ) Western blot analysis shows augmented expression of cleaved caspase 3 in arsenical-challenged mice. β-actin was used as an endogenous control. (D) Histogram representing densitometry analysis of western blots band intensity. (Also see supplementary fig. S4, S5 and S6 for full images of immunoblots). *P < 0.05, **P < 0.01,***P < 0.001, ****P < 0.0001 showing significance compared to vehicle treated controls. ns, non-significant. N = 3/group.

Article Snippet: Keyence Microscope inbuilt software (Model BZ-X710, KEYENCE, Osaka, Japan) was used for quantitative analysis of TUNEL-positive cells.

Techniques: TUNEL Assay, Microscopy, Software, Western Blot, Expressing, Control