| Place of Origin: | China |
|---|---|
| Brand Name: | ALLTEST |
| Model Number: | DFKE-102 |
| Minimum Order Quantity: | N/A |
| Price: | negotiation |
| Packaging Details: | 40T |
| Delivery Time: | 2-4 Weeks |
| Payment Terms: | Ex works |
| Supply Ability: | 10 M tests/month |
| Product Name: | A Rapid Test For The Qualitative Detection Of FKET In Human Urine. For Medical And Other Professional Use Only | Principle: | Chromatographic Immunoassay |
|---|---|---|---|
| Format: | Dipstick, Cassette, Panel | Specimen: | Urine |
| Reading Time: | 5 Minutes | Storage Temperature: | 2-30°C |
| Shelf Life: | 2 Years | Sensitivity: | 96.7% |
| Specificity: | 97.0% | Accuracy: | 96.9% |
| Cut-Off: | 1000 Ng/mL | Features 1: | Fast Results In 5 Minutes |
| Features 2: | Simple Visual Interpretation | Features 3: | Easy Urine Specimen Collection |
| Features 4: | Convenient Operation High Accuracy | ||
| High Light: | FKET Detection Test Panel,FKET Detection A Rapid Test,FKET Detection Drug Abuse Test Kit |
||
A rapid test for the qualitative detection of FKET in human urine. For medical and other professional use only
The FKET Rapid Test Cassette (Urine) is a rapid chromatographic immunoassay for the detection of F-Keta/mine in human urine at a cut-off concentration of 1000 ng/ml. This test will detect other related compounds, please refer to the Analytical Specificity table in this package insert.
This assay provides only a preliminary analytical test result. A more specific alternate chemical method must be used in order to obtain a confirmed analytical result. Gas chromatography/mass spectrometry (GC/MS) is the preferred confirmatory method. Clinical consideration and professional judgment should be applied to any drug of abuse test result, particularly when preliminary positive results are used.
F-Keta/mine is generally used as the replacement of keta/mine with hallucinogenic properties. When abused, people are immersed in anesthesia situation with distorting perceptions of sight and sound and feeling out of control1. Currently, there is limited research and using regulation of F-Keta/mine. Therefore, a large number of people abuse F-Keta/mine instead of keta/mine. But nowadays, the detection of F-Keta/mine is restricted to high performance liquid chromatography (HPLC), gas chromatograph-mass spectrometer (GC-MS), thin layer chromatography (TLC), etc. which require not only expensive equipment but professional analysis2. At the same time, high purity of test material and complex operation are necessary as well. Therefore, it is a tendency that the test methods of FKET become fast and convenient.
The FKET Rapid Test Cassette (Urine) is a rapid urine screening test that can be performed without the use of an instrument. The test utilizes a monoclonal antibody to selectively detect elevated levels of F-Keta/mine in urine. The FKET Rapid Test Cassette (Urine) yields a positive result when F-Keta/mine in urine exceeds 1000ng/ml.
The FKET Rapid Test Cassette (Urine) is a rapid chromatographic immunoassay based on the principle of competitive binding. Drugs which may be present in the urine specimen compete against the drug conjugate for binding sites on the antibody.
During testing, a urine specimen migrates upward by capillary action. F-Keta/mine, if present in the urine specimen below 1000 ng/ml, will not saturate the binding sites of the antibody coated particles in the test. The antibody coated particles will then be captured by immobilized F-Keta/mine conjugate and a visible colored line will show up in the test line region. The colored line will not form in the test line region if the F-Keta/mine level exceeds 1000 ng/ml because it will saturate all the binding sites of anti-F-Keta/mine antibodies.
A drug-positive urine specimen will not generate a colored line in the test line region, while a drug-negative urine specimen or a specimen containing a drug concentration less than the cut-off will generate a line in the test line region. To serve as a procedural control, a colored line will always appear at the control line region indicating that proper volume of specimen has been added and membrane wicking has occurred.
The test contains mouse monoclonal anti-F-Keta/mine antibody-coupled particles and F-Keta/mine-protein conjugate. A rabbit antibody is employed in the control line system.
· For medical and other professional in vitro diagnostic use only. Do not use after the expiration date.
· The test should remain in the sealed pouch until use.
· All specimens should be considered potentially hazardous and handled in the same manner as an infectious agent.
· The used test should be discarded according to local regulations.
| Product Name: | A rapid test for the qualitative detection of FKET in human urine. For medical and other professional use only |
| Format: | Dipstick, Cassette, Panel |
| Reading Time: | 5 Minutes |
| Shelf Life: | 2 Years |
| Specificity: | 97.00% |
| Cut-Off: | 1000 Ng/mL |
| Features 2: | Simple Visual Interpretation |
| Features 4: | Convenient Operation High Accuracy |
| Principle: | Chromatographic Immunoassay |
| Specimen: | Urine |
| Storage Temperature: | 2-30°C |
| Sensitivity: | 96.70% |
| Accuracy: | 96.90% |
| Features 1: | Fast Results In 5 Minutes |
| Features 3: | Easy Urine Specimen Collection |
【DIRECTIONS FOR USE】
Allow the test, urine specimen, and/or controls to reach room temperature (15-30ºC) prior to testing.
A procedural control is included in the test. A colored line appearing in the control line region (C) is considered an internal procedural control. It confirms sufficient specimen volume, adequate membrane wicking and correct procedural technique.
Control standards are not supplied with this kit; however, it is recommended that positive and negative controls be tested as good laboratory testing practice to confirm the test procedure and to verify proper test performance.
