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jc 1 mitomp detection kit  (Dojindo Labs)


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    Structured Review

    Dojindo Labs jc 1 mitomp detection kit
    ( A ) Volcano plot of differentially expressed genes (DEGs) in MFC cells (Control versus DDP + Zn 2+ ). ( B ) KEGG pathway enrichment of DEGs. ( C ) Quantification of extracellular dsDNA. ( D <t>)</t> <t>JC-1</t> staining assessed by fluorescence microscopy and flow cytometry. ( E ) γ-H2AX immunofluorescence staining. Scale bar, 20 μm. ( F ) ASC speck colocalization with AIM2, Caspase-1, Caspase-8, and RIPK1. Scale bars, 5 μm (overview) and 1 μm (enlarged). ( G ) Western blot analysis of necroptosis markers (RIPK1, p-RIPK1, MLKL, and p-MLKL) and PANoptosis-related proteins (AIM2 and ZBP1). ( H ) Western blot analysis of apoptosis executors (Caspase-8, Caspase-3, and cleaved forms). ( I ) Western blot analysis of pyroptosis markers (Caspase-1, GSDMD, and cleaved forms). ( J ) Cell viability after DDP + Zn 2+ combined with VX-765, Ac-DEVD-CHO, or Nec-1. ( K ) PANoptosis-related proteins in si AIM2 cells. ( L and M ) cGAS activity (L) and expression (M) under Zn 2+ treatment. ( N ) Violin plot of cGAS expression. ( O ) Western blot analysis of STING pathway (STING, p-STING, TBK1, p-TBK1, IRF3, and p-IRF3). ( P ) CIBERSORT analysis of immune cell infiltration. ( Q ) BMDC maturation (CD80 + CD86 + ) after different treatments. ( R ) Schematic of the DDP + Zn 2+ –induced ICD. Data in (C), (J), and (L) are mean ± SD. Statistical analysis for (C), (J), (L), (N), and (P) used a two-tailed unpaired Student’s t test. (R) was created in BioRender. Fei, G. (2026) https://BioRender.com/8ri399r . * P < 0.05.
    Jc 1 Mitomp Detection Kit, supplied by Dojindo Labs, used in various techniques. Bioz Stars score: 96/100, based on 232 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/detection+kit/JC-1+MitoMP+Detection+Kit/pmc13626044-424-1-8
    Average 96 stars, based on 232 article reviews
    jc 1 mitomp detection kit - by Bioz Stars, 2026-10
    96/100 stars

    Images

    1) Product Images from "Chemo-metallo nanodrivers for spatiotemporally controlled in situ vaccination"

    Article Title: Chemo-metallo nanodrivers for spatiotemporally controlled in situ vaccination

    Journal: Science Advances

    doi: 10.1126/sciadv.aee4577

    ( A ) Volcano plot of differentially expressed genes (DEGs) in MFC cells (Control versus DDP + Zn 2+ ). ( B ) KEGG pathway enrichment of DEGs. ( C ) Quantification of extracellular dsDNA. ( D ) JC-1 staining assessed by fluorescence microscopy and flow cytometry. ( E ) γ-H2AX immunofluorescence staining. Scale bar, 20 μm. ( F ) ASC speck colocalization with AIM2, Caspase-1, Caspase-8, and RIPK1. Scale bars, 5 μm (overview) and 1 μm (enlarged). ( G ) Western blot analysis of necroptosis markers (RIPK1, p-RIPK1, MLKL, and p-MLKL) and PANoptosis-related proteins (AIM2 and ZBP1). ( H ) Western blot analysis of apoptosis executors (Caspase-8, Caspase-3, and cleaved forms). ( I ) Western blot analysis of pyroptosis markers (Caspase-1, GSDMD, and cleaved forms). ( J ) Cell viability after DDP + Zn 2+ combined with VX-765, Ac-DEVD-CHO, or Nec-1. ( K ) PANoptosis-related proteins in si AIM2 cells. ( L and M ) cGAS activity (L) and expression (M) under Zn 2+ treatment. ( N ) Violin plot of cGAS expression. ( O ) Western blot analysis of STING pathway (STING, p-STING, TBK1, p-TBK1, IRF3, and p-IRF3). ( P ) CIBERSORT analysis of immune cell infiltration. ( Q ) BMDC maturation (CD80 + CD86 + ) after different treatments. ( R ) Schematic of the DDP + Zn 2+ –induced ICD. Data in (C), (J), and (L) are mean ± SD. Statistical analysis for (C), (J), (L), (N), and (P) used a two-tailed unpaired Student’s t test. (R) was created in BioRender. Fei, G. (2026) https://BioRender.com/8ri399r . * P < 0.05.
    Figure Legend Snippet: ( A ) Volcano plot of differentially expressed genes (DEGs) in MFC cells (Control versus DDP + Zn 2+ ). ( B ) KEGG pathway enrichment of DEGs. ( C ) Quantification of extracellular dsDNA. ( D ) JC-1 staining assessed by fluorescence microscopy and flow cytometry. ( E ) γ-H2AX immunofluorescence staining. Scale bar, 20 μm. ( F ) ASC speck colocalization with AIM2, Caspase-1, Caspase-8, and RIPK1. Scale bars, 5 μm (overview) and 1 μm (enlarged). ( G ) Western blot analysis of necroptosis markers (RIPK1, p-RIPK1, MLKL, and p-MLKL) and PANoptosis-related proteins (AIM2 and ZBP1). ( H ) Western blot analysis of apoptosis executors (Caspase-8, Caspase-3, and cleaved forms). ( I ) Western blot analysis of pyroptosis markers (Caspase-1, GSDMD, and cleaved forms). ( J ) Cell viability after DDP + Zn 2+ combined with VX-765, Ac-DEVD-CHO, or Nec-1. ( K ) PANoptosis-related proteins in si AIM2 cells. ( L and M ) cGAS activity (L) and expression (M) under Zn 2+ treatment. ( N ) Violin plot of cGAS expression. ( O ) Western blot analysis of STING pathway (STING, p-STING, TBK1, p-TBK1, IRF3, and p-IRF3). ( P ) CIBERSORT analysis of immune cell infiltration. ( Q ) BMDC maturation (CD80 + CD86 + ) after different treatments. ( R ) Schematic of the DDP + Zn 2+ –induced ICD. Data in (C), (J), and (L) are mean ± SD. Statistical analysis for (C), (J), (L), (N), and (P) used a two-tailed unpaired Student’s t test. (R) was created in BioRender. Fei, G. (2026) https://BioRender.com/8ri399r . * P < 0.05.

    Techniques Used: Control, Staining, Fluorescence, Microscopy, Flow Cytometry, Immunofluorescence, Western Blot, Analysis, Activity Assay, Expressing, Immune Cell, Two Tailed Test

    ( A ) Fluorescence images of ZHDG internalization in MFC cells. ( B ) Quantification of the intracellular ZHDG fluorescence intensity. ( C ) Viability of MFC cells across treatment groups. ( D ) Annexin V–FITC/PI staining (fluorescence and flow cytometry). ( E ) TEM images of ultrastructural damage in MFC cells. ( F ) Relative LDH release. ( G ) Intracellular ATP levels. ( H ) Immunofluorescence analysis of CRT exposure and HMGB1 release. ( I ) Zinpyr-1 staining in different treatment groups. ( J ) Quantification of JC-1 aggregates and monomers. ( K ) JC-1 staining (flow cytometry). ( L ) Extracellular dsDNA release. ( M ) Western blot analysis of necroptosis markers (RIPK1, p-RIPK1, MLKL, and p-MLKL) and AIM2. ( N ) Western blot analysis of pyroptosis markers (Caspase-1, GSDMD, and cleaved forms). ( O ) Western blot analysis of apoptosis executors (Caspase-8, Caspase-3, and cleaved forms). ( P ) Western blot analysis of PANoptosis-related proteins in si AIM2 MFC cells treated with ZHDG + NIR. ( Q ) Schematic of ZHDG under NIR photoactivation inducing AIM2-PANoptosome formation and ICD. Data in (B), (C), (F), (G), and (L) are mean ± SD. Statistical analysis for (B), (C), (F), (G), and (L) was performed using a two-tailed unpaired Student’s t test. (Q) was created in BioRender. Fei, G. (2026) https://BioRender.com/wcbo7ma .
    Figure Legend Snippet: ( A ) Fluorescence images of ZHDG internalization in MFC cells. ( B ) Quantification of the intracellular ZHDG fluorescence intensity. ( C ) Viability of MFC cells across treatment groups. ( D ) Annexin V–FITC/PI staining (fluorescence and flow cytometry). ( E ) TEM images of ultrastructural damage in MFC cells. ( F ) Relative LDH release. ( G ) Intracellular ATP levels. ( H ) Immunofluorescence analysis of CRT exposure and HMGB1 release. ( I ) Zinpyr-1 staining in different treatment groups. ( J ) Quantification of JC-1 aggregates and monomers. ( K ) JC-1 staining (flow cytometry). ( L ) Extracellular dsDNA release. ( M ) Western blot analysis of necroptosis markers (RIPK1, p-RIPK1, MLKL, and p-MLKL) and AIM2. ( N ) Western blot analysis of pyroptosis markers (Caspase-1, GSDMD, and cleaved forms). ( O ) Western blot analysis of apoptosis executors (Caspase-8, Caspase-3, and cleaved forms). ( P ) Western blot analysis of PANoptosis-related proteins in si AIM2 MFC cells treated with ZHDG + NIR. ( Q ) Schematic of ZHDG under NIR photoactivation inducing AIM2-PANoptosome formation and ICD. Data in (B), (C), (F), (G), and (L) are mean ± SD. Statistical analysis for (B), (C), (F), (G), and (L) was performed using a two-tailed unpaired Student’s t test. (Q) was created in BioRender. Fei, G. (2026) https://BioRender.com/wcbo7ma .

    Techniques Used: Fluorescence, Staining, Flow Cytometry, Immunofluorescence, Analysis, Western Blot, Two Tailed Test

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    ( A ) Representative images of EdU staining at 14–15 hpf. Orange: EdU-positive nuclei indicating cell proliferation. Blue: DAPI. No EdU signal was detected in the atrial siphon primordium (white dashed outline). Scale bar: 10 μm. n = 10. ( B ) Representative images of <t>TUNEL</t> staining at 15 hpf. ( B1 ) Positive control: DNase I pretreatment (20 U/ml, 10 min) induced DNA fragmentation. ( B2 ) Negative control: staining performed without terminal deoxynucleotidyl transferase (TdT) enzyme. ( B3 ) Experimental group: no detectable TUNEL signal in the atrial siphon primordium (white dashed outline). Scale bar: 10 μm. n = 10.
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    Vector Laboratories immpress hrp antirabbit igg peroxidase polymer detection kit
    ( A ) Representative images of EdU staining at 14–15 hpf. Orange: EdU-positive nuclei indicating cell proliferation. Blue: DAPI. No EdU signal was detected in the atrial siphon primordium (white dashed outline). Scale bar: 10 μm. n = 10. ( B ) Representative images of <t>TUNEL</t> staining at 15 hpf. ( B1 ) Positive control: DNase I pretreatment (20 U/ml, 10 min) induced DNA fragmentation. ( B2 ) Negative control: staining performed without terminal deoxynucleotidyl transferase (TdT) enzyme. ( B3 ) Experimental group: no detectable TUNEL signal in the atrial siphon primordium (white dashed outline). Scale bar: 10 μm. n = 10.
    Immpress Hrp Antirabbit Igg Peroxidase Polymer Detection Kit, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Image Search Results


    ( A ) Volcano plot of differentially expressed genes (DEGs) in MFC cells (Control versus DDP + Zn 2+ ). ( B ) KEGG pathway enrichment of DEGs. ( C ) Quantification of extracellular dsDNA. ( D ) JC-1 staining assessed by fluorescence microscopy and flow cytometry. ( E ) γ-H2AX immunofluorescence staining. Scale bar, 20 μm. ( F ) ASC speck colocalization with AIM2, Caspase-1, Caspase-8, and RIPK1. Scale bars, 5 μm (overview) and 1 μm (enlarged). ( G ) Western blot analysis of necroptosis markers (RIPK1, p-RIPK1, MLKL, and p-MLKL) and PANoptosis-related proteins (AIM2 and ZBP1). ( H ) Western blot analysis of apoptosis executors (Caspase-8, Caspase-3, and cleaved forms). ( I ) Western blot analysis of pyroptosis markers (Caspase-1, GSDMD, and cleaved forms). ( J ) Cell viability after DDP + Zn 2+ combined with VX-765, Ac-DEVD-CHO, or Nec-1. ( K ) PANoptosis-related proteins in si AIM2 cells. ( L and M ) cGAS activity (L) and expression (M) under Zn 2+ treatment. ( N ) Violin plot of cGAS expression. ( O ) Western blot analysis of STING pathway (STING, p-STING, TBK1, p-TBK1, IRF3, and p-IRF3). ( P ) CIBERSORT analysis of immune cell infiltration. ( Q ) BMDC maturation (CD80 + CD86 + ) after different treatments. ( R ) Schematic of the DDP + Zn 2+ –induced ICD. Data in (C), (J), and (L) are mean ± SD. Statistical analysis for (C), (J), (L), (N), and (P) used a two-tailed unpaired Student’s t test. (R) was created in BioRender. Fei, G. (2026) https://BioRender.com/8ri399r . * P < 0.05.

    Journal: Science Advances

    Article Title: Chemo-metallo nanodrivers for spatiotemporally controlled in situ vaccination

    doi: 10.1126/sciadv.aee4577

    Figure Lengend Snippet: ( A ) Volcano plot of differentially expressed genes (DEGs) in MFC cells (Control versus DDP + Zn 2+ ). ( B ) KEGG pathway enrichment of DEGs. ( C ) Quantification of extracellular dsDNA. ( D ) JC-1 staining assessed by fluorescence microscopy and flow cytometry. ( E ) γ-H2AX immunofluorescence staining. Scale bar, 20 μm. ( F ) ASC speck colocalization with AIM2, Caspase-1, Caspase-8, and RIPK1. Scale bars, 5 μm (overview) and 1 μm (enlarged). ( G ) Western blot analysis of necroptosis markers (RIPK1, p-RIPK1, MLKL, and p-MLKL) and PANoptosis-related proteins (AIM2 and ZBP1). ( H ) Western blot analysis of apoptosis executors (Caspase-8, Caspase-3, and cleaved forms). ( I ) Western blot analysis of pyroptosis markers (Caspase-1, GSDMD, and cleaved forms). ( J ) Cell viability after DDP + Zn 2+ combined with VX-765, Ac-DEVD-CHO, or Nec-1. ( K ) PANoptosis-related proteins in si AIM2 cells. ( L and M ) cGAS activity (L) and expression (M) under Zn 2+ treatment. ( N ) Violin plot of cGAS expression. ( O ) Western blot analysis of STING pathway (STING, p-STING, TBK1, p-TBK1, IRF3, and p-IRF3). ( P ) CIBERSORT analysis of immune cell infiltration. ( Q ) BMDC maturation (CD80 + CD86 + ) after different treatments. ( R ) Schematic of the DDP + Zn 2+ –induced ICD. Data in (C), (J), and (L) are mean ± SD. Statistical analysis for (C), (J), (L), (N), and (P) used a two-tailed unpaired Student’s t test. (R) was created in BioRender. Fei, G. (2026) https://BioRender.com/8ri399r . * P < 0.05.

    Article Snippet: The JC-1 MitoMP Detection Kit was obtained from Dojindo Molecular Technologies Inc. (Kumamoto, Japan).

    Techniques: Control, Staining, Fluorescence, Microscopy, Flow Cytometry, Immunofluorescence, Western Blot, Analysis, Activity Assay, Expressing, Immune Cell, Two Tailed Test

    ( A ) Fluorescence images of ZHDG internalization in MFC cells. ( B ) Quantification of the intracellular ZHDG fluorescence intensity. ( C ) Viability of MFC cells across treatment groups. ( D ) Annexin V–FITC/PI staining (fluorescence and flow cytometry). ( E ) TEM images of ultrastructural damage in MFC cells. ( F ) Relative LDH release. ( G ) Intracellular ATP levels. ( H ) Immunofluorescence analysis of CRT exposure and HMGB1 release. ( I ) Zinpyr-1 staining in different treatment groups. ( J ) Quantification of JC-1 aggregates and monomers. ( K ) JC-1 staining (flow cytometry). ( L ) Extracellular dsDNA release. ( M ) Western blot analysis of necroptosis markers (RIPK1, p-RIPK1, MLKL, and p-MLKL) and AIM2. ( N ) Western blot analysis of pyroptosis markers (Caspase-1, GSDMD, and cleaved forms). ( O ) Western blot analysis of apoptosis executors (Caspase-8, Caspase-3, and cleaved forms). ( P ) Western blot analysis of PANoptosis-related proteins in si AIM2 MFC cells treated with ZHDG + NIR. ( Q ) Schematic of ZHDG under NIR photoactivation inducing AIM2-PANoptosome formation and ICD. Data in (B), (C), (F), (G), and (L) are mean ± SD. Statistical analysis for (B), (C), (F), (G), and (L) was performed using a two-tailed unpaired Student’s t test. (Q) was created in BioRender. Fei, G. (2026) https://BioRender.com/wcbo7ma .

    Journal: Science Advances

    Article Title: Chemo-metallo nanodrivers for spatiotemporally controlled in situ vaccination

    doi: 10.1126/sciadv.aee4577

    Figure Lengend Snippet: ( A ) Fluorescence images of ZHDG internalization in MFC cells. ( B ) Quantification of the intracellular ZHDG fluorescence intensity. ( C ) Viability of MFC cells across treatment groups. ( D ) Annexin V–FITC/PI staining (fluorescence and flow cytometry). ( E ) TEM images of ultrastructural damage in MFC cells. ( F ) Relative LDH release. ( G ) Intracellular ATP levels. ( H ) Immunofluorescence analysis of CRT exposure and HMGB1 release. ( I ) Zinpyr-1 staining in different treatment groups. ( J ) Quantification of JC-1 aggregates and monomers. ( K ) JC-1 staining (flow cytometry). ( L ) Extracellular dsDNA release. ( M ) Western blot analysis of necroptosis markers (RIPK1, p-RIPK1, MLKL, and p-MLKL) and AIM2. ( N ) Western blot analysis of pyroptosis markers (Caspase-1, GSDMD, and cleaved forms). ( O ) Western blot analysis of apoptosis executors (Caspase-8, Caspase-3, and cleaved forms). ( P ) Western blot analysis of PANoptosis-related proteins in si AIM2 MFC cells treated with ZHDG + NIR. ( Q ) Schematic of ZHDG under NIR photoactivation inducing AIM2-PANoptosome formation and ICD. Data in (B), (C), (F), (G), and (L) are mean ± SD. Statistical analysis for (B), (C), (F), (G), and (L) was performed using a two-tailed unpaired Student’s t test. (Q) was created in BioRender. Fei, G. (2026) https://BioRender.com/wcbo7ma .

    Article Snippet: The JC-1 MitoMP Detection Kit was obtained from Dojindo Molecular Technologies Inc. (Kumamoto, Japan).

    Techniques: Fluorescence, Staining, Flow Cytometry, Immunofluorescence, Analysis, Western Blot, Two Tailed Test

    ( A ) Representative images of EdU staining at 14–15 hpf. Orange: EdU-positive nuclei indicating cell proliferation. Blue: DAPI. No EdU signal was detected in the atrial siphon primordium (white dashed outline). Scale bar: 10 μm. n = 10. ( B ) Representative images of TUNEL staining at 15 hpf. ( B1 ) Positive control: DNase I pretreatment (20 U/ml, 10 min) induced DNA fragmentation. ( B2 ) Negative control: staining performed without terminal deoxynucleotidyl transferase (TdT) enzyme. ( B3 ) Experimental group: no detectable TUNEL signal in the atrial siphon primordium (white dashed outline). Scale bar: 10 μm. n = 10.

    Journal: eLife

    Article Title: Bidirectional redistribution of actomyosin drives epithelial invagination in ascidian siphon tube morphogenesis

    doi: 10.7554/eLife.108588

    Figure Lengend Snippet: ( A ) Representative images of EdU staining at 14–15 hpf. Orange: EdU-positive nuclei indicating cell proliferation. Blue: DAPI. No EdU signal was detected in the atrial siphon primordium (white dashed outline). Scale bar: 10 μm. n = 10. ( B ) Representative images of TUNEL staining at 15 hpf. ( B1 ) Positive control: DNase I pretreatment (20 U/ml, 10 min) induced DNA fragmentation. ( B2 ) Negative control: staining performed without terminal deoxynucleotidyl transferase (TdT) enzyme. ( B3 ) Experimental group: no detectable TUNEL signal in the atrial siphon primordium (white dashed outline). Scale bar: 10 μm. n = 10.

    Article Snippet: Commercial assay, kit , TUNEL BrightRed Apoptosis Detection Kit , Vazyme , Cat#A113 , .

    Techniques: Staining, TUNEL Assay, Positive Control, Negative Control

    Journal: eLife

    Article Title: Bidirectional redistribution of actomyosin drives epithelial invagination in ascidian siphon tube morphogenesis

    doi: 10.7554/eLife.108588

    Figure Lengend Snippet:

    Article Snippet: Commercial assay, kit , TUNEL BrightRed Apoptosis Detection Kit , Vazyme , Cat#A113 , .

    Techniques: Cell-Signaling, Recombinant, Plasmid Preparation, TUNEL Assay, Cloning, Sequencing, Software