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大小鼠间歇氧浓度实验系统模仿睡眠呼吸暂停模式ProOx-10

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  • ¥27000 - 50000
  • 塔望科技
  • ProOx-100HE
  • 中国
  • 2026年01月21日
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    • 文献和实验
    • 技术资料
    • 库存

      大量

    • 国食药监械注册号

    • 保修期

      1年

    • 现货状态

      现货

    • 供应商

      塔望科技

    • 规格

      咨询电话:021-51537683/15221725700

    根据客户的需求不同,所对应的配套方案价格也不同!如果对这类产品感兴趣,可和我们联系。

    塔望科技提供全系列的动物实验用低/高氧控制产品,包括恒定浓度控制的低氧动物箱、高氧动物箱、可编程的间歇氧浓度控制系统、带缓冲舱的低氧箱等。整套低氧/高氧实验箱装置主要由氧气控制器和动物实验箱两部分组成。另可提供多种不同的气体控制器,满足不同实验O2、CO2、NO、CO、O3等气体浓度控制的需求。

    大小鼠间歇氧浓度实验系统模仿睡眠呼吸暂停模式是一款多功能的氧浓度控制系统,用户可以自定义设置氧气浓度变化的步骤,可实现恒定持续低氧、持续高氧、间歇低氧、急性缺氧、慢性间歇低氧、阶梯式氧浓度变化、周期性氧浓度控制等。所有的设置通过控制主机触摸屏完成,人性化设计,操作简便。

    大小鼠间歇氧浓度实验系统模仿睡眠呼吸暂停模式监测指标全面,动物低氧舱内具有集成化的传感器模块,内置温度、湿度、氧气、二氧化碳传感器。可以实时监测动物低氧舱内的环境。系统通过闭环反馈控制,根据动物低氧舱内的氧浓度实时反馈控制,使动物实验低氧数据更准确,避免了控制型浓度输出和低氧舱内浓度不一致的情况。ProOx-100HE动物间歇氧浓度实验系统具有优良的控制性能,持续低氧实验时,氧浓度的误差为0.1%。

    大小鼠间歇氧浓度实验系统模仿睡眠呼吸暂停模式提供不同尺寸的动物低氧箱,默认低氧箱可放置1个大鼠笼(或2个小鼠笼),同时提供大号规格,可容纳2个大鼠笼和4个大鼠笼。如需其它规格,可提供定制。

     

    大小鼠间歇氧浓度实验系统模仿睡眠呼吸暂停模式

    可进行间歇低氧实验(CIH)、急性缺氧实验、慢性缺氧实验、高氧/低氧交替实验

     

    大小鼠间歇氧浓度实验系统模仿睡眠呼吸暂停模式产品特点及参数:

    1.  为动物低氧、高氧实验模型的建立提供合适的气体环境

    2. 按照设定气体浓度自动配比气体,维持恒定的氧气浓度环境。无需在箱体外混合比例气体,确保实验氧浓度的准确,节省气源

    3. 低氧箱采用进口透明 PMMA材质,坚固耐用

    4. 7英寸大屏触摸屏控制,人性化界面,操作简单

    5. 具有多功能可编程控制器:动态控制,实现多种氧浓度控制方式,可进行急性缺氧实验、慢性缺氧实验、间歇式低氧等实验

    6. 监测参数:温度、湿度、氧气O2浓度、二氧化碳浓度

    7. 非色散红外(NDIR)二氧化碳传感器,测量范围:0~5000ppm测量精度:±30ppm

    8. 进口电化学氧气O2浓度检测器,测量范围:0-100%vol,测量分辨率:0.01%,线性度好,检测准确、使用寿命长。具有温度补偿机制

    9. 温度检测:进口高精度数字铂电阻温度传感器

    10. 氧气浓度变化动态曲线,直观了解氧气浓度变化的过程

    11. 氧气浓度自动校准:通过控制器对传感器快速校准

    12. 湿度传感器和除湿设计,能有效的降低动物实验过程中呼吸产生的水汽对动物的影响

    13. 特有的气体混合及循环机制,保证箱体内气体浓度的均一

    14. 高性能电磁阀,性能稳定,超长寿命

     

    大小鼠间歇氧浓度实验系统模仿睡眠呼吸暂停模式应用领域

    睡眠呼吸暂停综合症、心肌缺血缺氧、脑缺血损伤、肺动脉高压、高原反应、肿瘤、呼吸疾病、造血功能等多种领域的动物建模研究。

     

    大小鼠间歇氧浓度实验系统模仿睡眠呼吸暂停模式规格型号

    名称

    型号

    功能

    参考容纳动物数量

    备注

    动物间歇氧浓度实验系统

    ProOx-100HE

    多功能控制氧浓度

    大鼠:5-10只

    小鼠:20-30只

    可直接放1个大鼠笼、或2个小鼠笼

    动物间歇氧浓度实验系统

    ProOx-100HE-N

    多功能控制氧浓度

    具有恒温功能

    适合新生鼠

    新生鼠10-20只

    恒温功能,适合新生鼠

    舱体小

    动物间歇氧浓度实验系统

    ProOx-100HE-D

    多功能控制氧浓度

    大鼠:12-20只

    小鼠:40-60只

    可直接放2个大鼠笼、或4个小鼠笼

    动物间歇氧浓度实验系统

    ProOx-100HE-T

    多功能控制氧浓度

    大鼠:20-30只

    小鼠:60-90只

    系统自带动物专用鼠笼

    动物间歇氧浓度实验系统

    ProOx-100HE-MC

    多功能控制氧浓度

    双通道独立控制

     

    可选大鼠笼或小鼠笼

    豪华工具套装

    Kit-NV

     

     

    适合持续一个月间歇低氧的应用

    备注:

    所有动物低氧系统均可选择温度控制功能,维持低氧舱内温度恒定

    可选配光源控制,作为动物提供适合饲养的光源及模拟昼夜节律控制

    大小鼠间歇氧浓度实验系统模仿睡眠呼吸暂停模式客户代表名单

    图片4.png


    大小鼠间歇氧浓度实验系统模仿睡眠呼吸暂停模式相关文献

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    [2] Wu L W, Chen M, Jiang C Y, et al. Inactivation of AXL in Cardiac Fibroblasts Alleviates Right Ventricular Remodeling in Pulmonary Hypertension[J]. Advanced Science (IF 14.1), 2025: e08995.
    [3] Lei R, Gu M, Li J, et al. Lipoic acid/trometamol assembled hydrogel as injectable bandage for hypoxic wound healing at high altitude[J]. Chemical Engineering Journal (IF 13.4), 2024, 489: 151499.
    [4] Li Z, Li H, Qiao W, et al. Multi-omics dissection of high TWAS-active endothelial pathogenesis in pulmonary arterial hypertension: bridging single-cell heterogeneity, machine learning-driven biomarkers, and developmental reprogramming[J]. International Journal of Surgery (IF 10.1), 10.1097.
    [5] Pei Y, Huang L, Wang T, et al. Bone marrow mesenchymal stem cells loaded into hydrogel/nanofiber composite scaffolds ameliorate ischemic brain injury[J]. Materials Today Advances (IF 10), 2023, 17: 100349.
    [6] Wang Q, Liu J, Li R, et al. Macrophage κ-opioid receptor inhibits hypoxic pulmonary hypertension progression and right heart dysfunction via an SCD1-dependent anti-inflammatory response[J]. Genes & Diseases (IF 9.4), 2025: 101604.
    [7] Wang Y, Zhang R, Chen Q, et al. PPARγ Agonist Pioglitazone Prevents Hypoxia-induced Cardiac Dysfunction by Reprogramming Glucose Metabolism[J]. International Journal of Biological Sciences, 2024, 20(11): 4297.
    [8] Wang Y, Shen P, Wu Z, et al. Plasma Proteomic Profiling Reveals ITGA2B as a key regulator of heart health in high-altitude settlers[J]. Genomics, Proteomics & Bioinformatics, 2025: qzaf030.
    [9] Lan Y, Zhao S, Song Y, et al. Physicochemical properties of selenized quinoa protein hydrolysate and its regulatory effects on neuroinflammation and gut microbiota in hypoxic mice[J]. Journal of Future Foods, 2025.
    [10] Pan Z, Yao Y, Liu X, et al. Nr1d1 inhibition mitigates intermittent hypoxia-induced pulmonary hypertension via Dusp1-mediated Erk1/2 deactivation and mitochondrial fission attenuation[J]. Cell Death Discovery, 2024, 10(1): 459.
    [11] Zhou Y, Ni Z, Liu J, et al. Gut Microbiota‐Associated Metabolites Affected the Susceptibility to Heart Health Abnormality in Young Migrants at High‐Altitude: Gut Microbiota and Associated Metabolites Impart Heart Health in Plateau[C]//Exploration. 2025: 20240332.
    [12] Li C, Zhao Z, Jin J, et al. NLRP3-GSDMD-dependent IL-1β Secretion from Microglia Mediates Learning and Memory Impairment in a Chronic Intermittent Hypoxia-induced Mouse Model[J]. Neuroscience, 2024, 539: 51-65.
    [13] Yang W, Li M, Ding J, et al. High-altitude hypoxia exposure inhibits erythrophagocytosis by inducing macrophage ferroptosis in the spleen[J]. Elife, 2024, 12: RP87496.
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    • 作者
    • 内容
    • 询问日期
    图标文献和实验
    该产品被引用文献

    [1] Drekolia M K, Mettner J, Wang D, et al. Cystine import and oxidative catabolism fuel vascular growth and repair via nutrient-responsive histone acetylation[J]. Cell Metabolism (IF 30.9), 2025.
    [2] Wu L W, Chen M, Jiang C Y, et al. Inactivation of AXL in Cardiac Fibroblasts Alleviates Right Ventricular Remodeling in Pulmonary Hypertension[J]. Advanced Science (IF 14.1), 2025: e08995.
    [3] Lei R, Gu M, Li J, et al. Lipoic acid/trometamol assembled hydrogel as injectable bandage for hypoxic wound healing at high altitude[J]. Chemical Engineering Journal (IF 13.4), 2024, 489: 151499.
    [4] Li Z, Li H, Qiao W, et al. Multi-omics dissection of high TWAS-active endothelial pathogenesis in pulmonary arterial hypertension: bridging single-cell heterogeneity, machine learning-driven biomarkers, and developmental reprogramming[J]. International Journal of Surgery (IF 10.1), 10.1097.
    [5] Pei Y, Huang L, Wang T, et al. Bone marrow mesenchymal stem cells loaded into hydrogel/nanofiber composite scaffolds ameliorate ischemic brain injury[J]. Materials Today Advances (IF 10), 2023, 17: 100349.
    [6] Wang Q, Liu J, Li R, et al. Macrophage κ-opioid receptor inhibits hypoxic pulmonary hypertension progression and right heart dysfunction via an SCD1-dependent anti-inflammatory response[J]. Genes & Diseases (IF 9.4), 2025: 101604.
    [7] Wang Y, Zhang R, Chen Q, et al. PPARγ Agonist Pioglitazone Prevents Hypoxia-induced Cardiac Dysfunction by Reprogramming Glucose Metabolism[J]. International Journal of Biological Sciences, 2024, 20(11): 4297.
    [8] Wang Y, Shen P, Wu Z, et al. Plasma Proteomic Profiling Reveals ITGA2B as a key regulator of heart health in high-altitude settlers[J]. Genomics, Proteomics & Bioinformatics, 2025: qzaf030.
    [9] Lan Y, Zhao S, Song Y, et al. Physicochemical properties of selenized quinoa protein hydrolysate and its regulatory effects on neuroinflammation and gut microbiota in hypoxic mice[J]. Journal of Future Foods, 2025.
    [10] Pan Z, Yao Y, Liu X, et al. Nr1d1 inhibition mitigates intermittent hypoxia-induced pulmonary hypertension via Dusp1-mediated Erk1/2 deactivation and mitochondrial fission attenuation[J]. Cell Death Discovery, 2024, 10(1): 459.
    [11] Zhou Y, Ni Z, Liu J, et al. Gut Microbiota‐Associated Metabolites Affected the Susceptibility to Heart Health Abnormality in Young Migrants at High‐Altitude: Gut Microbiota and Associated Metabolites Impart Heart Health in Plateau[C]//Exploration. 2025: 20240332.
    [12] Li C, Zhao Z, Jin J, et al. NLRP3-GSDMD-dependent IL-1β Secretion from Microglia Mediates Learning and Memory Impairment in a Chronic Intermittent Hypoxia-induced Mouse Model[J]. Neuroscience, 2024, 539: 51-65.
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