Bioteke Brand High Accuracy Fecal Occult Blood Test Kit Rapid Stool Blood Cassette for Pathological Analysis
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- Supplier: Bioteke Corporation (wuxi) Co. Ltd.
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Product Overview
Description
Products Description
Fecal Occult Blood (FOB) Rapid Test Kit
In the fast-paced modern life, health issues are often ignored by us. However, some early signs of disease may show up in inconspicuous places, such as occult blood in the stool. Fecal occult blood (FOB) refers to the presence of trace amounts of blood in the stool, which is invisible to the naked eye, but may indicate digestive health problems, such as gastroenteritis, gastric ulcers, polyps, and even colorectal cancer.
This product is IVD and CE certified
Item | Fecal Occult Blood Rapid Test Kit | ||||||
Specimen | Human Stool | ||||||
Principle | Immunochromatography technology, double antibody sandwich method | ||||||
Test Items | Gastrointestinal bleeding, ulcers etc. | ||||||
Components | 1.Test Strip: NC membrane: coating hemoglobin monoclonal antibody and Anti-mouse IgG polyclonal antibody. Gold label pad：coating labeled hemoglobin monoclonal antibody monoclonal antibody. 2.Sampling extraction tube. 3.Sampling swab 4.Waste bag 5.User instruction manual. Note: Sample extraction tubes are aluminum foil sealed packages with desiccant inside. | ||||||
Storage Condition And Shelf Life | The test kit should be stored at 2℃~30℃, valid for 24 months. Sample extraction tube should be used as soon as possible within 1 hour after opening the foil pouch. | ||||||
Specimen Requirements | a. The sample collection container should be clean, pollution-free, and disposable. b. It is recommended to use fresh human fecal samples, which should avoid mixing with hemoglobin from sources other than the digestive tract. c. Women should not take samples during menstruation. d. Samples should be taken from multiple parts of the feces. e. After sample collection, it should be tested as soon as possible within 1 hour. | ||||||
Performance Characteristics | Coincidence Rate:90% Limit of Detection:the minimum detection limit is not higher than 200ng/mL. Analysis Specificity:100% | ||||||
Package Specification | 1Test/Kit, 2Tests/Kit ,5Tests/Kit, 20Tests/Kit. | ||||||
Warm Warning:The results of this kit can be used for clinical reference, but should not be used as the sole basis for clinical diagnosis and treatment, which should be considered in conjunction with the patient's symptoms/signs, medical history, other laboratory tests and response to treatment.
Operation Process
Result Read
【Positive】 Both "C" and "T" show red lines. The lines at "T" can be dark or light in color, both indicate positive
results.
【Negative】 Red line presents at 'C', no line at 'T'.
【Invalid】 No red line presents at 'C', regardless of whether line presents at 'T', the result is invalid and you
should retest by with a new test kit.
results.
【Negative】 Red line presents at 'C', no line at 'T'.
【Invalid】 No red line presents at 'C', regardless of whether line presents at 'T', the result is invalid and you
should retest by with a new test kit.
Company Profile
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Bioteke Biotechnology Co., Ltd. was founded in 2005. It has been committed to the extraction and analysis of nucleic acids. It adheres to the combination of independent research and development and the introduction of advanced foreign technologies. After decades of development, it has become a comprehensive life science
instrument/kit/technology. A comprehensive high-tech biotechnology enterprise serving in one, with products covering scientific research, clinical, diagnosis and other aspects. We have established R&D and production bases in Beijing, Shenzhen, and Jiangsu, and have hundreds of agents and distributors across the country.
After continuous efforts, the company has continued to receive honors and has been rated
as "Beijing High-tech Enterprise" and "Group Member Unit of China Medical and Biotechnology Association". It has applied for dozens of patents. At present, the company is applying for more than ten patents. It has not only obtained 3 Beijing New Technology and New Product (Service) Certificates, but also passed the ISO13485:2016 quality management system certificate issued by TUV of Germany. Our company's fully automatic nucleic acid extraction instrument has also obtained the EU IVDD registration certificate (registration code NL-CA002-2018-45625).
as "Beijing High-tech Enterprise" and "Group Member Unit of China Medical and Biotechnology Association". It has applied for dozens of patents. At present, the company is applying for more than ten patents. It has not only obtained 3 Beijing New Technology and New Product (Service) Certificates, but also passed the ISO13485:2016 quality management system certificate issued by TUV of Germany. Our company's fully automatic nucleic acid extraction instrument has also obtained the EU IVDD registration certificate (registration code NL-CA002-2018-45625).
If you need the original certificate, please contact our customer service.
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