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chemiscope6100 imaging system  (Clinx Science)


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    Structured Review

    Clinx Science chemiscope6100 imaging system
    Chemiscope6100 Imaging System, supplied by Clinx Science, used in various techniques. Bioz Stars score: 96/100, based on 3667 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/chemiluminescence+imaging+system/ChemiScope+6100+chemiluminescence+and+fluorescence+imaging+system/pmc13034767-64-6-9
    Average 96 stars, based on 3667 article reviews
    chemiscope6100 imaging system - by Bioz Stars, 2026-09
    96/100 stars

    Images

    Related Articles

    Imaging:

    Article Title: Saikosaponin D and paeoniflorin improve the HCC immune microenvironment via CLCF1/PD-L1 mediated crosstalk between CAFs and tumor cells.
    Article Snippet: .. Afterward, the membranes were cultivated with secondary antibodies (Table S1) at 37°C for 1.5 h. Finally, the membranes were visualized using ECL Plus super-sensitive luminescent liquid (P1050-100, Applygen, Beijing, China) and analyzed with a chemiluminescence imaging system (ChemiScope6100, CLINX, Shanghai, China). ..

    Article Title: DYRK1B Inhibition by AZ191 Sensitizes High-Grade Serous Ovarian Cancer to Niraparib Through Promoting Apoptosis and Ferroptosis
    Article Snippet: .. Protein bands were https://doi.org/10.3390/biomedicines14040939 visualized using ECL reagent, and grayscale value was detected with a chemiluminescence imaging system (ChemiScope 6100, Clinx Science Instruments Co., Ltd., Shanghai, China). ..

    Article Title: HE4 drives PD-L1 expression in myeloid cells via IFN-γR-JAK-STAT3 signaling to promote tumor immune evasion
    Article Snippet: .. Images were captured via a chemiluminescence imaging system (Clinx, Shanghai, China) for further analysis. ..

    Article Title: Prolactin Drives the Pathogenic Amplification of Atopic Dermatitis by Promoting CCL17 Secretion Through Activation of the PI3K/AKT Pathway.
    Article Snippet: Background: Atopic dermatitis (AD) is a chronic and relapsing inflammatory skin disorder driven by a combination of epidermal barrier dysfunction, immune dysregulation, and psychological stress.. Although neuroendocrine-immune interactions are known to contribute to the pathogenesis of AD, the key endocrine mediators and their molecular mechanisms require elucidation.. Prolactin (PRL), a stress-associated hormone with cytokine-like immunomodulatory properties, has not been fully characterized in the context of AD.

    Article Title: Mesenchymal stem cells inhibited chronic myeloid leukemia cells in vitro, correlating with oxidative stress.
    Article Snippet: After sealing with skim milk, membranes were incubated overnight at 4°C with primary antibodies, including anti-Nrf2 (Proteintech, 16396-1-AP, USA), anti-IκBα (Proteintech, 10268-1-AP, USA), and anti-GAPDH (Proteintech, 10494-1-AP, USA). .. Membranes were rinsed and incubated with a AR TIC LE IN PR ES S secondary IgG antibody (Proteintech, SA00001-2, USA) for 2 h. Protein bands were detected utilizing BeyoECL Plus (Ultra-sensitive ECL Chemiluminescence Kit) (Beyotime, P0018S, China) and chemiluminescence imaging system (Clinx, China). ..

    Article Title: Indazole derivative, and preparation method therefor and use thereof
    Article Snippet: After the membrane was transferred, the membrane was added in 1×QuickBlock blocking buffer (Beyotime) and incubated for 30 minutes at room temperature. .. After blocking, PVDF membranes were incubated with IRAK4 primary antibody (Abcam) overnight at 4°, the membranes were washed with TBST buffer (2.4 g Tris, 8.8 g NaCl, 1.5 mL Tween 20, pH adjusted to 7.4, constant volume to 1 L) for 30 minutes, incubated with secondary antibody (Abcam) for 2 hours at room temperature, finally incubated with Clarity Western ECL Substrate (BIO-RAD) for 5 minutes for luminescence development, chemiluminescence imaging system (Clinx, chemiScope 6200 Touch) was used for development and protein mapping photography. .. The protein map was analyzed by Clinx chemiluminescence analysis software for grayscale values.

    Article Title: Dual-targeting of mitochondrial and c-Myc G-quadruplexes by a photoactive coumarin-benzothiazolium conjugate inhibits triple-negative breast cancer cell growth.
    Article Snippet: Targeting G-quadruplexes (G4s) presents a promising strategy for cancer therapy, but early-generation ligands often lack tumor selectivity.. This study identified X-3, a novel photoactive coumarin-benzothiazolium conjugate, as a dual-targeted photosensitizer against triple-negative breast cancer (TNBC).. X-3 localized to both mitochondria and the nucleus, where it specifically bound to mitochondrial and c-Myc G4s with high affinity.

    Article Title: iPSC-derived exosomes promote diabetic wound healing by attenuating inflammatory responses.
    Article Snippet: AR TIC LE IN PR ES S ARTICLE IN PRESS (M21002S, Abmart, China) for 1 hour at room temperature. .. The blots were visualized using a chemiluminescence imaging system (ChemiScope 6100, Clinx, China) after SuperSignalTM West Pico Luminol/Enhancer Solution (34580, Thermo Fisher, USA) was added to the NC film. .. 2.8 Statistical analysis Statistical analysis was performed using GraphPad Prism software.

    Incubation:

    Article Title: Mesenchymal stem cells inhibited chronic myeloid leukemia cells in vitro, correlating with oxidative stress.
    Article Snippet: After sealing with skim milk, membranes were incubated overnight at 4°C with primary antibodies, including anti-Nrf2 (Proteintech, 16396-1-AP, USA), anti-IκBα (Proteintech, 10268-1-AP, USA), and anti-GAPDH (Proteintech, 10494-1-AP, USA). .. Membranes were rinsed and incubated with a AR TIC LE IN PR ES S secondary IgG antibody (Proteintech, SA00001-2, USA) for 2 h. Protein bands were detected utilizing BeyoECL Plus (Ultra-sensitive ECL Chemiluminescence Kit) (Beyotime, P0018S, China) and chemiluminescence imaging system (Clinx, China). ..

    Article Title: Indazole derivative, and preparation method therefor and use thereof
    Article Snippet: After the membrane was transferred, the membrane was added in 1×QuickBlock blocking buffer (Beyotime) and incubated for 30 minutes at room temperature. .. After blocking, PVDF membranes were incubated with IRAK4 primary antibody (Abcam) overnight at 4°, the membranes were washed with TBST buffer (2.4 g Tris, 8.8 g NaCl, 1.5 mL Tween 20, pH adjusted to 7.4, constant volume to 1 L) for 30 minutes, incubated with secondary antibody (Abcam) for 2 hours at room temperature, finally incubated with Clarity Western ECL Substrate (BIO-RAD) for 5 minutes for luminescence development, chemiluminescence imaging system (Clinx, chemiScope 6200 Touch) was used for development and protein mapping photography. .. The protein map was analyzed by Clinx chemiluminescence analysis software for grayscale values.

    Blocking Assay:

    Article Title: Indazole derivative, and preparation method therefor and use thereof
    Article Snippet: After the membrane was transferred, the membrane was added in 1×QuickBlock blocking buffer (Beyotime) and incubated for 30 minutes at room temperature. .. After blocking, PVDF membranes were incubated with IRAK4 primary antibody (Abcam) overnight at 4°, the membranes were washed with TBST buffer (2.4 g Tris, 8.8 g NaCl, 1.5 mL Tween 20, pH adjusted to 7.4, constant volume to 1 L) for 30 minutes, incubated with secondary antibody (Abcam) for 2 hours at room temperature, finally incubated with Clarity Western ECL Substrate (BIO-RAD) for 5 minutes for luminescence development, chemiluminescence imaging system (Clinx, chemiScope 6200 Touch) was used for development and protein mapping photography. .. The protein map was analyzed by Clinx chemiluminescence analysis software for grayscale values.

    Western Blot:

    Article Title: Indazole derivative, and preparation method therefor and use thereof
    Article Snippet: After the membrane was transferred, the membrane was added in 1×QuickBlock blocking buffer (Beyotime) and incubated for 30 minutes at room temperature. .. After blocking, PVDF membranes were incubated with IRAK4 primary antibody (Abcam) overnight at 4°, the membranes were washed with TBST buffer (2.4 g Tris, 8.8 g NaCl, 1.5 mL Tween 20, pH adjusted to 7.4, constant volume to 1 L) for 30 minutes, incubated with secondary antibody (Abcam) for 2 hours at room temperature, finally incubated with Clarity Western ECL Substrate (BIO-RAD) for 5 minutes for luminescence development, chemiluminescence imaging system (Clinx, chemiScope 6200 Touch) was used for development and protein mapping photography. .. The protein map was analyzed by Clinx chemiluminescence analysis software for grayscale values.



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    Servicebio Inc fluorescence chemiluminescence imaging system
    Gel-HMSN/GOx-LArg@IL promotes vascular neurogenesis and cell migration. A) Optical images of vascular formation by HUVECs subjected to different treatments. Scale bar: 200 μm. B) Cell migration experiments of HUVECs in different treatment groups. Scale bar: 200 μm. C) Immunofluorescence staining of β 3 -tubulin expression in BMSC cells of different treatment groups. Scale bar: 200 μm. D) Quantitative analysis of vascular length. E) Quantitative analysis of cell migration rate. F) Quantitative analysis of <t>fluorescence</t> intensity. Data are represented as mean ± SD (n = 3). Statistical analysis was performed using one-way analysis of variance (ANOVA) followed by Tukey's test ∗ p < 0.05. ∗∗ p < 0.01. ∗∗∗ p < 0.001. ∗∗∗∗ p < 0.0001.
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    Image Search Results


    Gel-HMSN/GOx-LArg@IL promotes vascular neurogenesis and cell migration. A) Optical images of vascular formation by HUVECs subjected to different treatments. Scale bar: 200 μm. B) Cell migration experiments of HUVECs in different treatment groups. Scale bar: 200 μm. C) Immunofluorescence staining of β 3 -tubulin expression in BMSC cells of different treatment groups. Scale bar: 200 μm. D) Quantitative analysis of vascular length. E) Quantitative analysis of cell migration rate. F) Quantitative analysis of fluorescence intensity. Data are represented as mean ± SD (n = 3). Statistical analysis was performed using one-way analysis of variance (ANOVA) followed by Tukey's test ∗ p < 0.05. ∗∗ p < 0.01. ∗∗∗ p < 0.001. ∗∗∗∗ p < 0.0001.

    Journal: Materials Today Bio

    Article Title: Multidimensional nano-ion composite hydrogel based on enzymatic blood glucose control, gas therapy and ion liquid permeation for repairing diabetic wounds

    doi: 10.1016/j.mtbio.2026.103213

    Figure Lengend Snippet: Gel-HMSN/GOx-LArg@IL promotes vascular neurogenesis and cell migration. A) Optical images of vascular formation by HUVECs subjected to different treatments. Scale bar: 200 μm. B) Cell migration experiments of HUVECs in different treatment groups. Scale bar: 200 μm. C) Immunofluorescence staining of β 3 -tubulin expression in BMSC cells of different treatment groups. Scale bar: 200 μm. D) Quantitative analysis of vascular length. E) Quantitative analysis of cell migration rate. F) Quantitative analysis of fluorescence intensity. Data are represented as mean ± SD (n = 3). Statistical analysis was performed using one-way analysis of variance (ANOVA) followed by Tukey's test ∗ p < 0.05. ∗∗ p < 0.01. ∗∗∗ p < 0.001. ∗∗∗∗ p < 0.0001.

    Article Snippet: Protein bands were visualized using a chemiluminescent substrate and imaged with a fluorescence & chemiluminescence imaging system (Servicebio).

    Techniques: Migration, Immunofluorescence, Staining, Expressing, Fluorescence

    Skin immunofluorescence staining and immunohistochemical analysis were performed in different treatment groups. A) Immunofluorescence staining images of NF200. β 3 -Tubulin. PGP9.5. CD31. VEGF and IL-6 in skin wounds on the 14th day after treatment. Scale = 400 μm. B) Immunohistochemical images of FGF2 on day 14 in wound tissue. Scale = 400 μm. C) Images of the immunohistochemistry of AGEs. Scale bar = 400 μm. D) Fluorescence intensity of NF200. E) Fluorescence intensity of β 3 Tubulin. F) Fluorescence intensity of PGP9.5. G) CD31-labeled micro vessel density. H) Fluorescence intensity of VEGF. I) Fluorescence intensity of IL-6. J) Integrated option density (IOD) of FGF2. K) IOD of AGEs. Data are represented as mean ± SD (n = 3). Statistical analysis was performed using one-way analysis of variance (ANOVA) followed by Tukey's test ∗ p < 0.05. ∗∗ p < 0.01. ∗∗∗ p < 0.001. ∗∗∗∗ p < 0.0001.

    Journal: Materials Today Bio

    Article Title: Multidimensional nano-ion composite hydrogel based on enzymatic blood glucose control, gas therapy and ion liquid permeation for repairing diabetic wounds

    doi: 10.1016/j.mtbio.2026.103213

    Figure Lengend Snippet: Skin immunofluorescence staining and immunohistochemical analysis were performed in different treatment groups. A) Immunofluorescence staining images of NF200. β 3 -Tubulin. PGP9.5. CD31. VEGF and IL-6 in skin wounds on the 14th day after treatment. Scale = 400 μm. B) Immunohistochemical images of FGF2 on day 14 in wound tissue. Scale = 400 μm. C) Images of the immunohistochemistry of AGEs. Scale bar = 400 μm. D) Fluorescence intensity of NF200. E) Fluorescence intensity of β 3 Tubulin. F) Fluorescence intensity of PGP9.5. G) CD31-labeled micro vessel density. H) Fluorescence intensity of VEGF. I) Fluorescence intensity of IL-6. J) Integrated option density (IOD) of FGF2. K) IOD of AGEs. Data are represented as mean ± SD (n = 3). Statistical analysis was performed using one-way analysis of variance (ANOVA) followed by Tukey's test ∗ p < 0.05. ∗∗ p < 0.01. ∗∗∗ p < 0.001. ∗∗∗∗ p < 0.0001.

    Article Snippet: Protein bands were visualized using a chemiluminescent substrate and imaged with a fluorescence & chemiluminescence imaging system (Servicebio).

    Techniques: Immunofluorescence, Staining, Immunohistochemical staining, Immunohistochemistry, Fluorescence, Labeling