Product Description
| Brand | Abbott |
| Sample Type | Serum/ Plasma/ WB |
| Pack Size | 25T |
| CAT No | 15FK12 |
Bioline Salmonella typhi IgG/IgM Fast test is an immunochromatographic assay for the rapid, qualitative and differential detection of IgG and IgM antibodies to Salmonella typhi in human serum, plasma or whole blood. This test provides only a preliminary test result. Therefore more specific alternative diagnostic methods must be used to confirm Salmonella typhi infection.
Fast and Reliable Typhoid DetectionThe Abbott Bioline SALMONELLA TYPHI IgG/IgM FAST offers rapid and dependable results for typhoid fever detection. Utilizing advanced LFIA technology, this kit provides visual positive or negative results in as little as 15 minutes. Broad sample compatibility-serum, plasma, or whole blood-ensures flexibility and ease of use across different clinical settings, making early diagnosis straightforward and accessible.
User-Friendly and Portable DesignEach test is individually packaged in a lightweight, plastic cassette for ease of transport and storage. With no instruments required and a clear visual result display, healthcare providers can efficiently conduct typhoid testing wherever it's needed. The test's straightforward manual operation and integrated procedural control further simplify workflow while ensuring accurate performance.
High Accuracy and Regulatory AssuranceThis rapid test kit is engineered for high sensitivity and specificity, exceeding 98% accuracy. CE IVD marking affirms its reliability and compliance with European diagnostic standards. It is designed for single use and maintains its efficacy throughout its 18-24 month shelf life, provided it is stored between 1C and 40C. This reliability ensures trustworthy screening for both acute and past Salmonella Typhi infections.
FAQ's of Abbott Bioline SALMONELLA TYPHI IgG/IgM FAST:
Q: How does the Abbott Bioline SALMONELLA TYPHI IgG/IgM FAST detect typhoid fever?
A: This rapid test employs Lateral Flow Immunochromatographic Assay (LFIA) technology to qualitatively detect IgG and IgM antibodies specific to Salmonella Typhi in a patient's serum, plasma, or whole blood. The presence of colored lines in the labeled test window indicates positive or negative results for each antibody type and includes a control for procedural accuracy.
Q: What sample types can be used with this rapid test kit?
A: You can use serum, plasma, or whole blood samples collected from human patients. This versatility supports testing in various clinical and field settings, minimizing the need for specialized collection processes.
Q: When should the results be interpreted after performing the test?
A: The test delivers results within 15 minutes of applying the sample. It is important to interpret the visual lines promptly within the specified time window to ensure the accuracy of the result.
Q: Where can this test be utilized effectively?
A: The portable, self-contained nature of this kit allows it to be used in clinics, hospitals, laboratories, field camps, or remote healthcare centers-any location where rapid and accurate diagnosis of typhoid fever is essential and access to laboratory equipment is limited.
Q: What steps are involved in using the Abbott Bioline SALMONELLA TYPHI IgG/IgM FAST kit?
A: Simply collect the patient's serum, plasma, or whole blood sample, apply it to the test cassette's sample well, and add the buffer provided. Wait 15 minutes, and then read the result by observing the colored lines for IgG, IgM, and the control line through the test window.
Q: What are the main benefits of this typhoid rapid test kit?
A: Key advantages include quick turnaround (15 minutes), ease of use, no instrument requirement, high accuracy (>98%), and compatibility with multiple sample types. Its portability and individually packed cassettes make it ideal for point-of-care testing and fast decision-making in diverse healthcare environments.
Q: How should the test kits be stored to ensure optimal performance?
A: Store the test kits at temperatures between 1C and 40C, avoiding direct sunlight and freezing. Following these instructions will maintain the test's efficacy throughout its shelf life of 18-24 months from the manufacturing date.