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  • 99
    Cell Signaling Technology Inc anti cleaved caspase 3
    Low-osmolar contrast media (LOCM) resulted in accumulations of apoptosis associated proteins in uninephrectomized mice. (A) Western blotting analysis of apoptosis associated proteins in uninephrectomized mice, which were randomly assigned to three groups: control group (4 weeks after uninephrectomy(UPHT)), 24 h water deprivation (dehy.) + furosemide (furo.) group, as well as 24 h water deprivation + furosemide + LOCM group. (B-D) The gray intensity analysis of western blotting of <t>cleaved</t> <t>caspase-3</t> (C- Casp 3), Bcl-2, and Bax. * p
    Anti Cleaved Caspase 3, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/anti cleaved caspase 3/product/Cell Signaling Technology Inc
    Average 99 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    anti cleaved caspase 3 - by Bioz Stars, 2022-11
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    99
    Abcam e cadherin
    Low-osmolar contrast media (LOCM) resulted in accumulations of apoptosis associated proteins in uninephrectomized mice. (A) Western blotting analysis of apoptosis associated proteins in uninephrectomized mice, which were randomly assigned to three groups: control group (4 weeks after uninephrectomy(UPHT)), 24 h water deprivation (dehy.) + furosemide (furo.) group, as well as 24 h water deprivation + furosemide + LOCM group. (B-D) The gray intensity analysis of western blotting of <t>cleaved</t> <t>caspase-3</t> (C- Casp 3), Bcl-2, and Bax. * p
    E Cadherin, supplied by Abcam, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/e cadherin/product/Abcam
    Average 99 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    e cadherin - by Bioz Stars, 2022-11
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    Image Search Results


    Low-osmolar contrast media (LOCM) resulted in accumulations of apoptosis associated proteins in uninephrectomized mice. (A) Western blotting analysis of apoptosis associated proteins in uninephrectomized mice, which were randomly assigned to three groups: control group (4 weeks after uninephrectomy(UPHT)), 24 h water deprivation (dehy.) + furosemide (furo.) group, as well as 24 h water deprivation + furosemide + LOCM group. (B-D) The gray intensity analysis of western blotting of cleaved caspase-3 (C- Casp 3), Bcl-2, and Bax. * p

    Journal: Renal Failure

    Article Title: A novel contrast-induced acute kidney injury mouse model based on low-osmolar contrast medium

    doi: 10.1080/0886022X.2022.2108449

    Figure Lengend Snippet: Low-osmolar contrast media (LOCM) resulted in accumulations of apoptosis associated proteins in uninephrectomized mice. (A) Western blotting analysis of apoptosis associated proteins in uninephrectomized mice, which were randomly assigned to three groups: control group (4 weeks after uninephrectomy(UPHT)), 24 h water deprivation (dehy.) + furosemide (furo.) group, as well as 24 h water deprivation + furosemide + LOCM group. (B-D) The gray intensity analysis of western blotting of cleaved caspase-3 (C- Casp 3), Bcl-2, and Bax. * p

    Article Snippet: The membranes were blocked with 5% skimmed milk in Tris-buffered saline and then incubated with primary anti-Caspase 3 (CST, Beverly, MA, USA), anti-Cleaved Caspase 3 (CST, Beverly, MA, USA), anti-Bcl-2 (Antibody Revolution, San Diego, CA, USA), anti-Bax (Abcam, Cambridge, MA, US), and anti-Tubulin (Proteintech, Chicago, IL, USA) antibodies.

    Techniques: Mouse Assay, Western Blot

    Frequency of CIC structures, senescent and apoptotic cells assessed by immunohistochemistry. a E-Cadherin staining labelling numerous CIC structures in HNSCC and magnifications of indicated region. (a i ) Schematic drawing of a CIC structure illustrating defining criteria: complete encirclement of the inner cell by the host cell membrane, circular shape of the inner cell and semilunar host cell nucleus. b Cleaved caspase-3 labeled HNSCC and magnifications of indicated region showing CIC structures negative for cleaved caspase-3. c H3K9ME labeled HNSCC showing senescent cells and magnifications of indicated region. d Ki67 labeled HNSCC showing proliferating cells and magnifications of indicated region. Comparative analysis of ( e ) CIC structures, ( f ) senescent cells, ( g ) apoptotic cells, ( h ) proliferating cells and ( j ) tumor cells in the center of the tumor (pre- and post-RCT) and invasive front (pre-RCT). k Comparison of ratio of CIC structures, senescent cells and apoptotic cells in the center of the tumor and invasive front compared to frequency of CIC structures in the center of the tumor pre-RCT as a reference

    Journal: Radiation Oncology (London, England)

    Article Title: Cell-in-cell structures are more potent predictors of outcome than senescence or apoptosis in head and neck squamous cell carcinomas

    doi: 10.1186/s13014-016-0746-z

    Figure Lengend Snippet: Frequency of CIC structures, senescent and apoptotic cells assessed by immunohistochemistry. a E-Cadherin staining labelling numerous CIC structures in HNSCC and magnifications of indicated region. (a i ) Schematic drawing of a CIC structure illustrating defining criteria: complete encirclement of the inner cell by the host cell membrane, circular shape of the inner cell and semilunar host cell nucleus. b Cleaved caspase-3 labeled HNSCC and magnifications of indicated region showing CIC structures negative for cleaved caspase-3. c H3K9ME labeled HNSCC showing senescent cells and magnifications of indicated region. d Ki67 labeled HNSCC showing proliferating cells and magnifications of indicated region. Comparative analysis of ( e ) CIC structures, ( f ) senescent cells, ( g ) apoptotic cells, ( h ) proliferating cells and ( j ) tumor cells in the center of the tumor (pre- and post-RCT) and invasive front (pre-RCT). k Comparison of ratio of CIC structures, senescent cells and apoptotic cells in the center of the tumor and invasive front compared to frequency of CIC structures in the center of the tumor pre-RCT as a reference

    Article Snippet: Four consecutive cancer sections were stained with E-cadherin for CIC detection (Fig. ), anti-cleaved caspase-3 for detection of apoptosis (Fig. ), anti-H3K9Me for detection of senescence (Fig. ) and anti-Ki67 for identification of proliferating cells (Fig. ).

    Techniques: Immunohistochemistry, Staining, Labeling

    Bergmann glia apoptosis (a–g) representative images of cleaved-caspase-3 immunolabeling. Objective 20×. (a) Sham. (b) PCA. (c) PCA+NH 3 . (d) PCA+LPS. (e) PCA+NH 3 +LPS. (f) Representative image of cleaved-caspase-3 immunolabeling and Nissl counterstain, the double stain reveals cell death of Bergmann glia (BG; arrow) in Purkinje cell layer (P). Objective 60×. (g) Bar diagram represents mean intensity value of caspase-3 inmunostaining. * P ≤ 0.05 compared to sham. PCA: portacaval anastomosis; LPS: lipopolysaccharide.

    Journal: Journal of Cerebral Blood Flow & Metabolism

    Article Title: Cerebellar neurodegeneration in a new rat model of episodic hepatic encephalopathy

    doi: 10.1177/0271678X16649196

    Figure Lengend Snippet: Bergmann glia apoptosis (a–g) representative images of cleaved-caspase-3 immunolabeling. Objective 20×. (a) Sham. (b) PCA. (c) PCA+NH 3 . (d) PCA+LPS. (e) PCA+NH 3 +LPS. (f) Representative image of cleaved-caspase-3 immunolabeling and Nissl counterstain, the double stain reveals cell death of Bergmann glia (BG; arrow) in Purkinje cell layer (P). Objective 60×. (g) Bar diagram represents mean intensity value of caspase-3 inmunostaining. * P ≤ 0.05 compared to sham. PCA: portacaval anastomosis; LPS: lipopolysaccharide.

    Article Snippet: Apoptosis was assessed using cleaved-caspase-3 antibody (anti-casp3 (Asp175); 1/600, Cell Signalling, Danvers, MA, USA).

    Techniques: Immunolabeling, Staining