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  • 94
    Olympus olympus dp70 camera
    HPSE-degraded cell surface HSGAG promotes angiogenesis in vivo . Blood vessel density was assessed by counting vessels within the tumor region in five different sections in each tumor. Tumor sections were photographed using Olympus <t>DP70</t> camera, Olympus
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    Olympus dp70 olympus digital camera
    HPSE-degraded cell surface HSGAG promotes angiogenesis in vivo . Blood vessel density was assessed by counting vessels within the tumor region in five different sections in each tumor. Tumor sections were photographed using Olympus <t>DP70</t> camera, Olympus
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    Olympus photometric sensys olympus dp70 ccd camera
    HPSE-degraded cell surface HSGAG promotes angiogenesis in vivo . Blood vessel density was assessed by counting vessels within the tumor region in five different sections in each tumor. Tumor sections were photographed using Olympus <t>DP70</t> camera, Olympus
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    Olympus built in olympus dp70 12 5 mpx digital camera
    HPSE-degraded cell surface HSGAG promotes angiogenesis in vivo . Blood vessel density was assessed by counting vessels within the tumor region in five different sections in each tumor. Tumor sections were photographed using Olympus <t>DP70</t> camera, Olympus
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    HPSE-degraded cell surface HSGAG promotes angiogenesis in vivo . Blood vessel density was assessed by counting vessels within the tumor region in five different sections in each tumor. Tumor sections were photographed using Olympus <t>DP70</t> camera, Olympus
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    Olympus dp70 olympus digital microscope camera
    HPSE-degraded cell surface HSGAG promotes angiogenesis in vivo . Blood vessel density was assessed by counting vessels within the tumor region in five different sections in each tumor. Tumor sections were photographed using Olympus <t>DP70</t> camera, Olympus
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    Olympus olympus dp70 12 5 mpa digital camera
    HPSE-degraded cell surface HSGAG promotes angiogenesis in vivo . Blood vessel density was assessed by counting vessels within the tumor region in five different sections in each tumor. Tumor sections were photographed using Olympus <t>DP70</t> camera, Olympus
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    Olympus fluorescent microscope olympus dp70 digital camera
    HPSE-degraded cell surface HSGAG promotes angiogenesis in vivo . Blood vessel density was assessed by counting vessels within the tumor region in five different sections in each tumor. Tumor sections were photographed using Olympus <t>DP70</t> camera, Olympus
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    Olympus megapixel cooled olympus dp70 digital color camera
    HPSE-degraded cell surface HSGAG promotes angiogenesis in vivo . Blood vessel density was assessed by counting vessels within the tumor region in five different sections in each tumor. Tumor sections were photographed using Olympus <t>DP70</t> camera, Olympus
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    Olympus bright field microscope olympus bx 50 olympus dp70 camera cell
    HPSE-degraded cell surface HSGAG promotes angiogenesis in vivo . Blood vessel density was assessed by counting vessels within the tumor region in five different sections in each tumor. Tumor sections were photographed using Olympus <t>DP70</t> camera, Olympus
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    Olympus bx21 microscope olympus dp70 camera
    HPSE-degraded cell surface HSGAG promotes angiogenesis in vivo . Blood vessel density was assessed by counting vessels within the tumor region in five different sections in each tumor. Tumor sections were photographed using Olympus <t>DP70</t> camera, Olympus
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    Olympus colour olympus dp70 digital camera
    HPSE-degraded cell surface HSGAG promotes angiogenesis in vivo . Blood vessel density was assessed by counting vessels within the tumor region in five different sections in each tumor. Tumor sections were photographed using Olympus <t>DP70</t> camera, Olympus
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    Image Search Results


    HPSE-degraded cell surface HSGAG promotes angiogenesis in vivo . Blood vessel density was assessed by counting vessels within the tumor region in five different sections in each tumor. Tumor sections were photographed using Olympus DP70 camera, Olympus

    Journal:

    Article Title: Cell Surface Heparan Sulfate Released by Heparanase Promotes Melanoma Cell Migration and Angiogenesis

    doi: 10.1002/jcb.22005

    Figure Lengend Snippet: HPSE-degraded cell surface HSGAG promotes angiogenesis in vivo . Blood vessel density was assessed by counting vessels within the tumor region in five different sections in each tumor. Tumor sections were photographed using Olympus DP70 camera, Olympus

    Article Snippet: Tumor sections were photographed using Olympus DP70 camera, Olympus BX45 microscope and saved in JPEG format using DP Manager (Olympus America Inc., Center Valley, PA).

    Techniques: In Vivo

    Transduction of the denatured Tat-SOD protein into mouse skin and IHC staining of SNP-induced cyclooxygenase-2 (COX-2) and nitrotyrosine protein expression. Dorsal skins of female ICR mice were treated topically with acetone (as the vehicle control) or indicated concentrations of Tat-SOD, celecoxib, or PTIO for 2 h before SNP (20 μmol/200 μL/site) treatment for 4 h. All samples were applied to the backs of animals in 200 μL acetone using an adjustable pipette (1 cm in diameter) and the effect of Tat-SOD on mouse skin was assayed with an IHC study. Finally, immunohistograms were taken with an Olympus DP-70 camera on a Nikon ECLIPSE E800 microscope (at an original magnification of × 200). a His-tag staining. b COX-2 protein staining. c Nitrotyrosine protein staining. Arrows indicate positive His-tag, COX-2, and nitrotyrosine staining which produced a brown-colored product

    Journal: Journal of Biomedical Science

    Article Title: Therapeutic evaluation of HIV transduction basic domain-conjugated superoxide dismutase solution on suppressive effects of the formation of peroxynitrite and expression of COX-2 in murine skin

    doi: 10.1186/s12929-016-0226-7

    Figure Lengend Snippet: Transduction of the denatured Tat-SOD protein into mouse skin and IHC staining of SNP-induced cyclooxygenase-2 (COX-2) and nitrotyrosine protein expression. Dorsal skins of female ICR mice were treated topically with acetone (as the vehicle control) or indicated concentrations of Tat-SOD, celecoxib, or PTIO for 2 h before SNP (20 μmol/200 μL/site) treatment for 4 h. All samples were applied to the backs of animals in 200 μL acetone using an adjustable pipette (1 cm in diameter) and the effect of Tat-SOD on mouse skin was assayed with an IHC study. Finally, immunohistograms were taken with an Olympus DP-70 camera on a Nikon ECLIPSE E800 microscope (at an original magnification of × 200). a His-tag staining. b COX-2 protein staining. c Nitrotyrosine protein staining. Arrows indicate positive His-tag, COX-2, and nitrotyrosine staining which produced a brown-colored product

    Article Snippet: Images were captured using an Olympus DP-70 camera on a Nikon ECLIPSE E800 microscope (at an original magnification of × 200).

    Techniques: Transduction, Immunohistochemistry, Staining, Expressing, Mouse Assay, Transferring, Microscopy, Produced

    Expression of HPV16E6 and E7 is associated with TNFR1 down-regulation. The expression of DR4 and TNFR1 was determined by immunofluorescence in control (pLXSN) and HPV16 E6/E7 transduced PHKs. Control or HPV16 E6E7 expressing keratinocytes were seeded in 8 wells Lab-Tek chambers, fixed, permeabilized and incubated with anti-DR4 ( A ) or anti-TNFR1 ( B ). After washing, cells were incubated with FITC-conjugated anti-mouse and mounted with Vectashield mounting medium for fluorescence with DAPI. Images were obtained with an Olympus BX61, with attached DP70 Olympus camera and its own software (Olympus, Japan). Magnification: 200×. ( C ) TNFR1 levels were determined by western blot in total protein extracts obtained from the same cells. Relative proteins signals were quantified using ImageJ software.

    Journal: International Journal of Molecular Sciences

    Article Title: HPV-Mediated Resistance to TNF and TRAIL Is Characterized by Global Alterations in Apoptosis Regulatory Factors, Dysregulation of Death Receptors, and Induction of ROS/RNS

    doi: 10.3390/ijms20010198

    Figure Lengend Snippet: Expression of HPV16E6 and E7 is associated with TNFR1 down-regulation. The expression of DR4 and TNFR1 was determined by immunofluorescence in control (pLXSN) and HPV16 E6/E7 transduced PHKs. Control or HPV16 E6E7 expressing keratinocytes were seeded in 8 wells Lab-Tek chambers, fixed, permeabilized and incubated with anti-DR4 ( A ) or anti-TNFR1 ( B ). After washing, cells were incubated with FITC-conjugated anti-mouse and mounted with Vectashield mounting medium for fluorescence with DAPI. Images were obtained with an Olympus BX61, with attached DP70 Olympus camera and its own software (Olympus, Japan). Magnification: 200×. ( C ) TNFR1 levels were determined by western blot in total protein extracts obtained from the same cells. Relative proteins signals were quantified using ImageJ software.

    Article Snippet: Images were obtained with an Olympus BX61 microscope, with an attached DP70 Olympus camera and its own software (Olympus, Tokyo, Japan).

    Techniques: Expressing, Immunofluorescence, Incubation, Fluorescence, Software, Western Blot