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大號動物低氧實驗系統

簡要描述:塔望科技提供全系列的動物實驗用低/高氧控制產品,包括恒定濃度控制的低氧動物箱、高氧動物箱、可編程的間歇氧濃度控制系統、帶緩沖艙的手套低氧箱等。整套低氧/高氧實驗箱裝置主要由氧氣控制器和動物實驗箱兩部分組成。另可提供多種不同的氣體控制器,滿足不同實驗O2、CO2、NO、CO、O3等氣體濃度控制的需求。

  • 產品型號:OX-100
  • 廠商性質:生產廠家
  • 更新時間:2026-01-20
  • 訪  問  量:2068

詳細介紹

品牌其他品牌產地類別國產
應用領域醫療衛生

產品描述

塔望科技提供全系列的動物實驗用低/高氧控制產品,包括恒定濃度控制的低氧動物箱、高氧動物箱、可編程的間歇氧濃度控制系統、帶緩沖艙的手套低氧箱等。整套低氧/高氧實驗箱裝置主要由氧氣控制器和動物實驗箱兩部分組成。另可提供多種不同的氣體控制器,滿足不同實驗O2、CO2、NO、CO、O3等氣體濃度控制的需求。

Ox-100動物低氧實驗系統可以控制動物實驗箱內持續低氧的環境,用以制造相關的低氧實驗模型。用戶可自由設置所需要的濃度和實驗持續時間,所有的設置通過控制主機觸摸屏完成,人性化設計,操作簡便。

Ox-100動物低氧實驗系統監測指標全面,動物低氧艙內具有集成化的傳感器模塊,內置溫度、濕度、氧氣、二氧化碳傳感器。可以實時監測動物低氧艙內的環境。系統通過閉環反饋控制,根據動物低氧艙內的氧濃度實時反饋控制,使動物實驗低氧數據更準確,避免了控制型濃度輸出和低氧艙內濃度不一致的情況。Ox-100動物低氧實驗系統具有優良的控制性能,持續低氧實驗時,氧濃度的誤差為0.1%

Ox-100動物低氧實驗系統提供不同尺寸的動物低氧箱,默認低氧箱可放置1個大鼠籠(或2個小鼠籠),同時提供大號規格,可容納2個大鼠籠和4個大鼠籠。如需其它規格,可提供定制。

如需高氧實驗,請選擇型號Ox-100HE

產品特點及參數

1. 為動物低氧實驗模型的建立提供穩定的低氧環境

2. 按照設定氣體濃度自動配比氣體,維持恒定的氧氣濃度環境。無需在箱體外混合比例氣體,實驗氧濃度的準確,節省氣源

3. 艙體采用全透明PMMA材質,防止由于光線影響動物生物節律

4. 7英寸大屏觸摸屏控制,人性化界面,操作簡單

5. 監測參數:溫度、濕度、氧氣O2濃度、二氧化碳濃度

6. 控制精度:±0.1%

7. 非色散紅外(NDIR)二氧化碳傳感器,測量范圍:05000ppm

8. 進口電化學氧氣O2濃度檢測器,測量范圍:0-25%vol,線性度好,檢測準確、使用壽命長。具有溫度補償機制

9. 溫度檢測:進口高精度溫度傳感器

10. 氧氣濃度變化動態曲線,直觀了解氧氣濃度變化的過程

11. 具有定時功能,實驗完成,自動恢復常氧狀態,并伴有聲音提示

12. 氧氣濃度自動校準:通過控制器對傳感器快速校準

13. *的氣體混合及循環機制,保證箱體內氣體濃度的均一

14. 高性能電磁閥,性能穩定,超長壽命

15. 艙體尺寸有多種選擇,可靈活搭配。也可根據實驗要求進行定制



ProOx-100動物間歇低氧實驗系統多功能控制


可進行間歇低氧實驗(CIH)、急性缺氧實驗、慢性缺氧實驗、高氧/低氧交替實驗



大號動物低氧實驗系統


應用領域

肺動脈高壓、腎臟疾病研究、腫瘤研究、心血管疾病研究、視網膜病變、運動醫學研究、OSAHS、腦發育與神經生物學、干細胞研究、醫學研究等

型號說明


名稱

型號

說明

單位

動物低氧實驗系統

Ox-100

恒定氧控制,低氧

動物氧濃度實驗系統

Ox-100HE

恒定氧控制,低氧/高氧

動物間歇低氧實驗系統

ProOx-100

恒定氧控制/間歇氧控制,低氧

動物間歇氧濃度實驗系統

ProOx-100HE

恒定氧控制/間歇氧控制,低氧/高氧


艙體型號(可選擇不同尺寸的低氧艙)

名稱

型號

說明

單位

動物實驗艙體小號

OxC-S

大鼠籠x1

動物實驗艙體中號

OxC-M

大鼠籠x2

動物實驗艙體大號

OxC-L

大鼠籠x4

動物實驗艙體特大號

OxC-XL

大鼠籠x8

動物實驗艙體-CIH

OxC-CIH

36只小鼠

手套操作箱

Gl-700

700L


*我公司可提供3Q驗證,根據客戶的特殊應用、特殊需求提供功能定制服務,也可以提供相關的實驗服務,詳情請來電問詢

引用文獻

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[22] Shang W, Huang Y, Xu Z, et al. The impact of a high-carbohydrate diet on the cognitive behavior of mice in a low-pressure, low-oxygen environment[J]. Food & Function, 2025, 16(3): 1116-1129.

[23] Pei C, Jia N, Wang Y, et al. Notoginsenoside R1 protects against hypobaric hypoxia-induced high-altitude pulmonary edema by inhibiting apoptosis via ERK1/2-P90rsk-BAD ignaling pathway[J]. European Journal of Pharmacology, 2023, 959: 176065.

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[27] Luan X, Zhu D, Hao Y, et al. Qibai Pingfei Capsule ameliorated inflammation in chronic obstructive pulmonary disease (COPD) via HIF-1 α/glycolysis pathway mediated of BMAL1[J]. International Immunopharmacology, 2025, 144: 113636.

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[29] Chang P, Xu M, Zhu J, et al. Pharmacological Inhibition of Mitochondrial Division Attenuates Simulated High‐Altitude Exposure‐Induced Memory Impairment in Mice: [30] Involvement of Inhibition of Microglia‐Mediated Synapse Elimination[J]. CNS Neuroscience & Therapeutics, 2025, 31(6): e70473.

[30] Liu C, Qu D, Li C, et al. miR‐448‐3p/miR‐1264‐3p Participates in Intermittent Hypoxic Response in Hippocampus by Regulating Fam76b/hnRNPA2B1[J]. CNS Neuroscience & Therapeutics, 2025, 31(2): e70239.

[31] Wu L W, Chen M, Jiang D J, et al. TCF7 enhances pulmonary hypertension by boosting stressed natural killer cells and their interaction with pulmonary arterial smooth muscle cells[J]. Respiratory Research, 2025, 26(1): 202.

[32] Xie L, Wu Q, Huang H, et al. Neuroregulation of histamine of circadian rhythm disorder induced by chronic intermittent hypoxia[J]. European Journal of Pharmacology, 2025: 177662.

[33] Cai S, Li Z, Bai J, et al. Optimized oxygen therapy improves sleep deprivation-induced cardiac dysfunction through gut microbiota[J]. Frontiers in Cellular and Infection Microbiology, 2025, 15: 1522431.

[34] Wang X, Xie Y, Niu Y, et al. CX3CL1/CX3CR1 signal mediates M1-type microglia and accelerates high-altitude-induced forgetting[J]. Frontiers in Cellular Neuroscience, 2023, 17: 1189348.

[35] He Y, Wang Y, Duan H, et al. Pharmacological targeting of ferroptosis in hypoxia-induced pulmonary edema: therapeutic potential of ginsenoside Rg3 through activation of the PI3K/AKT pathway[J]. Frontiers in Pharmacology, 2025, 16: 1644436.

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[41] Yao Y, Chen Y, Li Y, et al. TGM2 Enhances Hypobaric Hypoxia-mediated Brain Injury Via Regulating NLRP3/GSDMD Signaling[J]. Neurochemical Research, 2025, 50(6): 1-11.

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[47] Su L, Ni T, Fan R, et al. An attention to the effect of intravitreal injection on the controls of oxygen-induced retinopathy mouse model[J]. Experimental Eye Research, 2024, 248: 110094.

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