Product Description
Product details
| CAT No : | RK026-30 |
| Country of Origin | Made in India |
| Brand | SD Biosensor |
| ICMR Approved | Yes |
| Number of Reactions(Preps)/Kit | 30T |
| Result Time (Rapid Kits) | 10 min |
- Easy to use, Easy to read and interpret
- Room temperature storage
- Performance
- Sensitivity : 100% (43/43) / Specificity : 100% (162/162)
Fast and Accurate Hepatitis B ScreeningThe STANDARD Q HBsAg Rapid Test employs advanced immunochromatographic technology, allowing healthcare professionals to rapidly detect Hepatitis B surface antigen within 15-20 minutes. With sensitivity and specificity rates above 99%, it ensures dependable accuracy, making it ideal for early and reliable infection screening in hospitals, clinics, and laboratories.
Effortless Testing and Simple OperationThis diagnostic kit simplifies the screening process-requiring only serum, plasma, or whole blood. The test features a clear visual readout with built-in control, enabling straightforward interpretation without additional equipment. With its single-use, disposable format, it guarantees hygiene and safety for both users and patients.
Flexible Storage and Long Shelf LifeDesigned for convenience, the STANDARD Q HBsAg Rapid Test can be stored at room temperature (2C - 30C), making it practical for a variety of clinical settings. The device maintains high performance with a reliable shelf life of 18-24 months from the date of manufacture, ensuring you can keep it readily available whenever testing is needed.
FAQ's of STANDARD Q Hbsag:
Q: How does the STANDARD Q HBsAg Rapid Test work?
A: The STANDARD Q HBsAg Rapid Test uses lateral flow immunochromatographic technology to detect the presence of Hepatitis B surface antigen (HBsAg) in human serum, plasma, or whole blood. When a sample is applied with the buffer, the test cassette develops colored lines that visually indicate a positive or negative result within 15-20 minutes.
Q: What specimen types can be used with this test kit?
A: You can use human serum, plasma, or whole blood samples with the STANDARD Q HBsAg Rapid Test, offering flexibility for various clinical collection protocols.
Q: When should the test be performed after collecting the sample?
A: It is recommended to perform the test immediately after sample collection to ensure optimal sensitivity and reliable results. Delayed testing can affect accuracy, especially if the sample is not stored properly.
Q: Where is this test intended to be used?
A: This rapid test is primarily intended for use in hospitals and medical laboratories. Due to its portable, manual design and simple operation, it can also be utilized in clinics or mobile screening settings.
Q: What is the process for performing the test?
A: Following the provided instructions, add the collected sample and buffer to the test cassette's sample well. Wait for 15-20 minutes, and then visually inspect the result by checking the appearance of colored lines which indicate positive or negative HBsAg detection.
Q: What are the key benefits of using the STANDARD Q HBsAg Rapid Test?
A: Key benefits include rapid results, simple operation without laboratory instruments, high accuracy (>99% sensitivity and specificity), portability, and ease of storage at room temperature. Its single-use design ensures safety and reduces contamination risks.
Q: How should the test kits be stored for optimal performance?
A: Store the kits between 2C and 30C in a dry location away from sunlight and moisture. Ensure the packaging remains sealed until use to preserve product integrity for up to 18-24 months.