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| AsiaGen Rapid Array®HBV Detection Kit is a target-amplified nucleic acid probing test for in vitro diagnosis of HBV infection. It can accurately detect HBV nucleic acid from the clinical samples. AsiaGen HBV Detection Kit includes target (nucleic acid) amplification and sequence verification to maximize the detection Interpretation of the Result: ● Measure the RLU of positive and negative control first ● RLU ≧ 100,000, Positive for HBV presence. ● RLU < 25,000, Negative for HBV presence ● RLU falls between 25,000 and 100,000, repeat the test. ● If the repeated RLU is greater than or equal to 25,000, it will be interpreted as positive. If the repeated RLU is less than 25,000, it will be interpreted as negative for HBV presence Limitation of the Method: ● This test is for in vitro diagnostic use only. ● As with all diagnostic tests, a definitive clinical diagnosis should not be based on the result of a single test, but should only be made by the physician after all clinical and laboratory findings have been evaluated. ● Further confirmation method is required whenever necessary. |
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| AsiaGen Rapid Array®HBV Detection Kit is a target-amplified nucleic acid probing test for in vitro diagnosis of HBV infection. It can accurately detect HBV nucleic acid from the clinical samples. AsiaGen HBV Detection Kit includes target (nucleic acid) amplification and sequence verification to maximize the detection Interpretation of the Result: ● Measure the RLU of positive and negative control first ● RLU ≧ 100,000, Positive for HBV presence. ● RLU < 25,000, Negative for HBV presence ● RLU falls between 25,000 and 100,000, repeat the test. ● If the repeated RLU is greater than or equal to 25,000, it will be interpreted as positive. If the repeated RLU is less than 25,000, it will be interpreted as negative for HBV presence Limitation of the Method: ● This test is for in vitro diagnostic use only. ● As with all diagnostic tests, a definitive clinical diagnosis should not be based on the result of a single test, but should only be made by the physician after all clinical and laboratory findings have been evaluated. ● Further confirmation method is required whenever necessary. |
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