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        ROS-ID® Hypoxia/Oxidative stress detection ki

        更新時間:2022-01-28

        簡要描述:

        ROS-ID® Hypoxia/Oxidative stress detection kit Specific detection system for simultaneous analysis of hypoxia and oxidative stress using microscopy and flow cytometry

        型號:廠商性質:代理商瀏覽量:1296
        • Specifically distinguishes hypoxia from oxidative stress in Real-time

        • High sensitivity, specificity and accuracy for live cell studies

        • Use with adherent or suspension cell lines

        • Complete set of reagents, including ROS and Hypoxia inducer controls.

        Enzo Life Sciences’ ROS-ID® Hypoxia/Oxidative stress detection kit is designed for functional detection of hypoxia and oxidative stress levels in live cells (both suspension and adherent) using fluorescent microscopy or flow cytometry. This kit includes fluorogenic probes for hypoxia (red) and for oxidative stress levels (green) as two major components.

        The Hypoxia (Red) dye takes advantage of the nitroreductase activity present in hypoxic cells by converting the Nitro group to hydroxylamine (NHOH) and amino (NH2) and releasing the fluorescent probe.

        The Oxidative Stress Detection Reagent is a non-fluorescent, cell-permeable total ROS detection dye which reacts directly with a wide range of reactive species. The generated fluorescent products can be visualized using a wide-field fluorescence microscope equipped with standard fluorescein (490/525 nm) and Texas Red (596/670 nm) filters, confocal microscopy, or cytometrically using any flow cytometer equipped with a blue (488 nm) laser.
        ROS-ID® Hypoxia/Oxidative stress detection kit Fig3
        Detection of hypoxia and oxidative stress levels in cultured human HeLa and HL-60 cells. Cells were treated with hypoxia inducer (DFO) and ROS inducer (pyocyanin). Numbers in each quadrant reflects the percentage of cells (population). Results indicate that hypoxia and oxidative stress dye are specific
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        ROS-ID® Hypoxia/Oxidative stress detection kit Fig3ROS-ID® Hypoxia/Oxidative stress detection kit Fig2ROS-ID® Hypoxia/Oxidative stress detection kit Flow Cytometry


        Product Details

        Applications:Flow Cytometry, Fluorescence microscopy, Fluorescent detection, HTS

        Application Notes:This kit is designed for fluorescence microscopy and/or flow cytometry using adherent or suspension cells.

        Quality Control:The testing is accomplished using flow cytometry method for assessment of hypoxic cells and/or cells with high levels of total oxidative stress in conjunction with dyes (provided in kit). Microscopy images are also obtained.

        Quantity:For -K500 size:
        500 fluorescence microscopy assays or 100 flow cytometry assays.

        For -0125 size:
        125 fluorescence microscopy assays or 25 flow cytometry assays.

        Use/Stability:With proper storage, the kit components are stable up to the date noted on the product label.

        Handling:Avoid freeze/thaw cycles.

        Shipping:Shipped on Dry Ice

        Short Term Storage:-20°C

        Long Term Storage:-20°C

        Contents:Hypoxia Red Detection Reagent
        Oxidative Stress Detection Reagent (Green)
        ROS Inducer (Pyocyanin)
        Hypoxia Inducer (DFO)

        Technical Info/Product Notes:The ROS-ID® Hypoxia/Oxidative stress detection kit is a member of the CELLESTIAL® product line, reagents and assay kits comprising fluorescent molecular probes that have been extensively benchmarked for live cell analysis applications. CELLESTIAL® reagents and kits are optimal for use in demanding cell analysis applications involving confocal microscopy, flow cytometry, microplate readers and HCS/HTS, where consistency and reproducibility are required.

        Application Notes:
        3D Culture Application: Inhibition of Hypoxic Tumor Cells using a Three-Dimensional Spheroid Model

        3D Culture Application: PMT and Image-Based Analysis of Hypoxia Induction using a 3D Spheroid Model

        Protocol:Detailed instructions are included in the manual for microscopy and flow cytometry applications for adherent and suspension cells.

        Regulatory Status:RUO - Research Use Only

        Product Literature References

        Exploiting the acquired vulnerability of cisplatin-resistant tumors with a hypoxia-amplifying DNA repair-inhibiting (HYDRI) nanomedicine: J. Chen, et al.; Sci. Adv. 7, 5267 (2021), Abstract;
        Immune/Hypoxic Tumor Microenvironment Regulation-Enhanced Photodynamic Treatment Realized by pH-Responsive Phase Transition-Targeting Nanobubbles: M. Zhao, et al.; ACS Appl. Mater. Interfaces 13, 32763 (2021), Abstract;
        The New Serum-Free OptiPASS ® Medium in Cold and Oxygen-Free Conditions: An Innovative Conservation Method for the Preservation of MDA-MB-231 Triple Negative Breast Cancer Spheroids: A. Goisnard, et al.; Cancers 13, 1945 (2021), Abstract; Full Text
        Biomimetic decoy inhibits tumor growth and lung metastasis by reversing the drawbacks of sonodynamic therapy: H. Zhao, et al.; Adv. Healthc. Mater. 9, e1901335 (2020), Application(s): Fluorescence microscopy using 4T1 cells, Abstract;
        Remodeling extracellular matrix based on functional covalent organic framework to enhance tumor photodynamic therapy: S.B. Wang, et al.; Biomaterials 234, 119772 (2020), Application(s): Fluorescence microscopy using CT26 cells, Abstract;
        A two-photon excited O2-evolving nanocomposite for efficient photodynamic therapy against hypoxic tumor: R.Q. Li, et al.; Biomaterials 194, 84 (2019), Application(s): Fluorescence microscopy using 4T1 cells, Abstract;
        Combinational phototherapy and hypoxia-activated chemotherapy favoring antitumor immune responses: B. Ma, et al.; Int. J. Nanomedicine 14, 4541 (2019), Application(s): Fluorescence microscopy using 4T1 cells, Abstract; Full Text
        Di-(2-ethylhexyl) phthalate (DEHP) inhibits steroidogenesis and induces mitochondria-ROS mediated apoptosis in rat ovarian granulosa cells: A. Tripathi, et al.; Toxicol. Res. (Camb.) 8, 381 (2019), Application(s): Flow cytometry using granulosa cells, Abstract;


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