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上海康世达医疗器械有限公司 主营产品:医用体检,诊断,急救,化验,超声,医学分析,生命科学,消毒灭菌,康复治疗,手术室,急救室,诊疗室等设备,一类医疗器械,二类医疗器械,三类医疗器械,IVD及消毒器具耗材

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厂商直销佰瑞全自动免疫印迹仪BeeBlot48,BeeBlot20

价格:¥ 电议

品牌名称:$brandModel.Title型号: 原产地:中国大陆 医疗器械注册号(批文):国械注进20182221994更新时间:2026/10/16 11:11:09

产品摘要:厂商直销佰瑞全自动免疫印迹仪BeeBlot48,BeeBlot20

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详细内容

厂商直销佰瑞全自动免疫印迹仪BeeBlot48,BeeBlot20
桂经理19117326863微xin同号
桂经理19117326863微xin同号

管理类别

第二类

型号规格

BeeBlot48、BeeBlot20

结构及组成/主要组成成分

该产品由显示器单元、控制面板单元、蠕动泵单元、试剂瓶单元、机械臂单元、板槽单元、选配温控模


块单元和软件(发布版本号:V2)组成。

适用范围/预期用途

该产品基于免疫印迹原理(Western Blot),与配套的检测试剂共同使用,在临床上用于对来源于人体


的血浆、血清样本中的被分析物进行定性检测,包括用于自身免疫性疾病、传染性疾病和变态反应性疾


病诊断的抗原和抗体项目。

1、工作原理 Working Principle

中文:基于免疫印迹(Western‑Blot)固相免疫反应原理;仪器通过可编程蠕动泵系统自动分配样本、洗涤液、一抗、二抗等试剂;温控摇摆孵育平台控制膜条孵育温度、震荡模式与时长;抗原‑抗体在固相膜条上发生特异性免疫结合,完成封闭、孵育、洗涤全过程;最终膜条显色后,可人工判读或外接成像系统读取条带信号,实现人体样本待测抗体 / 抗原的定性检测。 English:Based on Western‑Blot solid‑phase immunoassay principle. The programmable peristaltic pump automatically dispenses samples, washing buffer, primary and secondary antibodies. Temperature‑controlled rocking incubation platform controls incubation temperature, shaking mode and duration. Specific antigen‑antibody binding occurs on solid‑phase strips to complete blocking, incubation and washing. After strip color development, results can be read manually or by external imaging system for qualitative detection of target antigens or antibodies in human samples。

2、产品功能 Functions

中文

  1. 自动完成免疫印迹实验全流程:试剂加注、孵育震荡、多次洗涤、膜条干燥;

  2. PID 温控孵育,支持试剂预热;

  3. 多套自定义实验程序编辑、存储、调用;

  4. 管道自动清洗维护程序;

  5. 兼容不同规格免疫印迹膜条,自动完成批量样本处理;

  6. 可外接成像设备输出实验结果,支持对接实验室信息系统 LIS。 English

  7. Fully automatic workflow for immunoblotting: reagent dispensing, incubation‑rocking, repeated washing and strip drying.

  8. PID precise temperature‑controlled incubation with reagent pre‑heating function.

  9. Edit, store and recall multiple custom assay protocols.

  10. Automatic pipeline cleaning & maintenance program.

  11. Compatible with various immunoblot strips for batch sample processing.

  12. Connectable with external imaging device for result output, supporting LIS laboratory information system connection.

3、产品特点 Product Features

中文

  1. 高通量:BeeBlot20 单次最多处理 20 条膜条;BeeBlot48 单次最多处理 48 条膜条;

  2. 开放平台:兼容市面主流免疫印迹试剂盒膜条,无需专用封闭耗材;

  3. 节约试剂:蠕动泵分液,降低试剂消耗量;

  4. 密闭实验环境,减少操作人员接触感染性样本风险;

  5. PID 温控,孵育温度均匀稳定;平台支持摇摆、倾斜多种孵育姿态;

  6. 操作简单,程序可视化编辑;自动管路清洗,降低交叉污染,维护便捷;

  7. 液晶键盘人机交互,无需外接电脑也可单机运行。 English

  8. High‑throughput: BeeBlot20 max.20 strips per run; BeeBlot48 max.48 strips per run.

  9. Open‑system design, compatible with mainstream commercial immunoblot kits without dedicated closed consumables.

  10. Reagent‑saving: precise peristaltic‑pump dispensing to reduce reagent consumption.

  11. Closed experimental environment to reduce operator exposure risk to infectious samples.

  12. PID temperature control for stable uniform incubation temperature; platform supports rocking & tilting incubation modes.

  13. Easy‑to‑use visual protocol editing; automatic pipeline cleaning reduces cross‑contamination with simple maintenance.

  14. LCD & keypad human‑machine interface, standalone operation without external computer.

4、技术参数 Technical Parameters

中文

表格

项目BeeBlot20BeeBlot48
单次处理膜条数最多 20 条最多 48 条
温控方式PID 闭环控温PID 闭环控温
温控精度±1℃±1℃
孵育模式摇摆、倾斜静置摇摆、倾斜静置
显示屏2 行 16 字符液晶显示屏2 行 16 字符液晶显示屏
操作界面薄膜按键键盘薄膜按键键盘
试剂分配精度≤10%≤10%
电源AC100‑240V,50‑60HzAC100‑240V,50‑60Hz
执行标准YY0648,GB4793.1YY0648,GB4793.1

English

表格

ItemsBeeBlot20BeeBlot48
Max strips per run20 strips48 strips
Temperature controlPID closed‑loop controlPID closed‑loop control
Temperature accuracy±1℃±1℃
Incubation modeRocking / tilting staticRocking / tilting static
Display2‑line 16‑character LCD2‑line 16‑character LCD
Operation interfaceMembrane keypadMembrane keypad
Dispensing accuracy≤10%≤10%
Power supplyAC100‑240V,50‑60HzAC100‑240V,50‑60Hz
Compliance standardYY0648,GB4793.1YY0648,GB4793.1

5、使用方法 Operation Method

中文

  1. 开机自检,确认仪器管路、孵育平台无异常;

  2. 根据试剂盒说明书,新建 / 调用对应实验程序,设置孵育时间、温度、洗涤次数、分液体积;

  3. 将印迹膜条放置于孵育托盘,安装到位;

  4. 装入样本、洗涤液、一抗、二抗等配套试剂;

  5. 启动运行,仪器自动完成分液、孵育震荡、洗涤、干燥全流程;

  6. 实验结束,取出膜条,进行显色判读或成像扫描;

  7. 执行管路自动清洗程序,完成后关机,做好设备使用记录。 English

  8. Power‑on self‑test, confirm pipeline and incubation platform in normal condition.

  9. Create or recall assay protocol according to kit instructions; set incubation time, temperature, washing cycles and dispensing volume.

  10. Place immunoblot strips correctly on incubation tray.

  11. Load samples, washing buffer, primary antibody, secondary antibody and other matched reagents.

  12. Start run; instrument automatically performs dispensing, rocking incubation, washing and drying.

  13. After run completion, take out strips for color‑development reading or imaging scanning.

  14. Run automatic pipeline cleaning procedure, power off and complete equipment usage record.


6、适应症 Indications

中文:本仪器与配套免疫印迹试剂盒联合使用,用于医疗机构检验科,对人体血清、血浆样本中抗原、抗体进行定性体外检测;适用于自身抗体谱检测、感染性疾病抗体确认试验、过敏原特异性抗体检测等体外免疫印迹实验。 English:Used together with matched immunoblot kits in clinical laboratory departments for in‑vitro qualitative detection of antigens and antibodies in human serum and plasma. Applicable for auto‑antibody profile testing, confirmatory assay for infectious disease antibodies, allergen‑specific antibody detection and other in‑vitro immunoblot tests.

7、禁忌症 Contraindications

中文:本设备为体外诊断实验分析仪器,无直接对患者使用的禁忌症;不可用于人体体内检测;不可使用严重溶血、脂血、变质失效的样本进行检测。 English:This device is an in‑vitro diagnostic analyzer, no contraindications for direct patient use. Not for in‑vivo human testing. Samples with severe hemolysis, lipemia or deterioration shall not be tested.


8、注意事项 Precautions

中文

  1. 仅可在医疗机构检验室内使用,操作人员需要熟悉免疫印迹实验操作;

  2. 样本多为潜在传染性标本,操作全程做好生物安全防护;

  3. 必须使用配套合格试剂与完好膜条,过期、变质试剂禁止使用;

  4. 定期执行管路清洗,防止试剂残留造成交叉污染;

  5. 温控孵育平台禁止硬物磕碰,避免管路弯折堵塞;

  6. 仪器出现报警故障,应停止实验,排查故障,必要时联系厂家维修,禁止私自拆机;

  7. 环境温湿度需满足设备运行条件,远离强电磁干扰源;

  8. 仪器仅作为实验自动化处理平台,检测结果必须结合临床、质控综合判读,不能单独作为确诊依据。 English

  9. Only used in clinical laboratory by operators familiar with immunoblot assay.

  10. Most samples are potentially infectious; biosafety protection shall be implemented throughout operation.

  11. Only use qualified matched reagents and intact strips; expired or deteriorated reagents are prohibited.

  12. Perform regular pipeline cleaning to avoid cross‑contamination caused by reagent residue.

  13. Prevent hard‑object collision on incubation platform; avoid pipeline bending and blockage.

  14. Stop testing when alarm occurs; troubleshoot or contact manufacturer for maintenance; disallow unauthorized disassembly.

  15. Operate under qualified ambient temperature & humidity; keep away from strong electromagnetic interference source.

  16. The instrument is only an automatic processing platform. Test results shall be interpreted combined with clinical information and quality‑control data and shall not be the sole basis for diagnosis.

9、存储条件 Storage Conditions

中文

  • 存储环境温度:5℃~40℃;

  • 相对湿度:20%‑85%,无冷凝;

  • 环境:干燥通风,避免粉尘、腐蚀性气体、阳光直射;运输存储避免剧烈撞击与倾倒;长期闲置前完成管路清洗。 English

  • Storage temperature:5℃~40℃;

  • Relative humidity:20%‑85%, non‑condensing;

  • Store in dry & ventilated environment, avoid dust, corrosive gas and direct sunlight. Prevent violent impact or tilting during transportation & storage. Complete pipeline cleaning before long‑term idle storage.


10、说明书核心摘要 Core Summary

中文:佰瑞 BeeBlot20 / BeeBlot48 全自动免疫印迹仪,为体外诊断免疫印迹自动化处理设备,依靠蠕动泵分液、温控摇摆孵育平台,自动完成免疫印迹膜条的加样、孵育、洗涤、干燥;开放兼容主流试剂盒,实现高通量样本前处理;仪器仅完成实验操作流程,不直接输出诊断结论,检测结果需结合质控与临床综合判断;严格执行生物安全防护,定期管路维护清洗,按说明书规定环境存储、使用。 English:BeeBlot20 / BeeBlot48 automatic immunoblot analyzer is an in‑vitro diagnostic automatic processing instrument. It adopts peristaltic‑pump reagent dispensing and temperature‑controlled rocking incubation platform to automatically complete sample loading, incubation, washing and drying for immunoblot strips. Open‑system compatible with mainstream kits for high‑throughput sample pretreatment. The instrument only performs experimental procedures and does not output diagnostic conclusions directly. Test results shall be comprehensively judged combined with quality‑control and clinical data. Strict biosafety protection, regular pipeline maintenance and cleaning shall be performed. Store and operate under environment specified in official manual.

免责声明:以上产品详情仅供参考,临床操作请以原厂纸质说明书为准。上海康世达医疗器械有限公司不生产医疗产品,所有产品均来自产品的生产厂家,代理商,经销商,如有侵权请联系我们,会尽快处理!The above product details are for reference only. All clinical operations shall be carried out in strict accordance with the original paper instructions for use issued by the manufacturer.
Shanghai Kangshida Medical Devices Co., Ltd. does not manufacture medical devices. All products are sourced from respective manufacturers, authorized agents and distributors.
Please contact us promptly in case of any infringement, and we will resolve the matter as soon as possible.

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