Myoglobin Whole Blood/Serum/Plasma Test (Cassette) GBR-3315
SKU: GBR-3315 Category: Rapid Tests
(BUP) Buprenorphine Test (Cassette) GBR-3414
sold under the trade names Subutex,Buprenex,Temgesic and Suboxone, which contain Buprenorphine HCl alone or in combination with Naloxone HCl.Therapeutically, Buprenorphine is used as a substitution treatment for opioid addicts. Substitution treatment is a form of medical care offered to opiate addicts (primarily heroin addicts) based on a similar or identical substance to the drug normally used 1.Application Buprenorphine (BUP) Single Drug Test Cassette is a rapid urine drug screening test that can be performed without the use of an instrument. Buprenorphine is a potent analgesic often used in the treatment of opioid addiction.The drug is sold under the trade names Subutex,Buprenex,Temgesic and Suboxone, which contain Buprenorphine HCl alone or in combination with Naloxone HCl.Therapeutically, Buprenorphine is used as a substitution treatment for opioid addicts. Substitution treatment is a form of medical care offered to opiate addicts (primarily heroin addicts) based on a similar or identical substance to the drug normally used. 2.Principle Buprenorphine (BUP) Drug Test Device is an 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. One Step Buprenorphine Drug Test Device is a rapid urine drug screening test that can be performed without the use of an instrument.During testing,a urine specimen migrates upward by capillary action. Buprenorphine, if present in the urine specimen below 10 ng/mL,will not saturate the binding sites of antibody-coated particles in the test. The antibody-coated particles will then be captured by immobilized Buprenorphine 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 Buprenorphine level exceeds 10 ng/mL because it will saturate all the binding sites of anti-Buprenorphine antibodies. A drug-positive urine specimen will not generate a colored line in the test line region because of drug competition,while a drug-negative urine specimen or a specimen containing a drug concentration lower 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.
Bladder Cancer Test (Cassette) GBR-3214
The Rapid ResponseTM Bladder Tumor Antigen Test Cassette is a lateral flow chromatographic immunoassay for the qualitative detection of bladder tumor antigen in human urine. It is intended to aid in the diagnosis and management of bladder cancer patients. In practice, patient urine is added to the sample well and allowed to react with a colloidal gold-conjugated antibody. Interpretation of test results are: positive (two lines), negative (one line), invalid (no lines or no Control line).
(BUP) Buprenorphine Test (Strip) GBR-3415
ALLTEST Buprenorphine BUP urine drug testing stripsKey points about Buprenorphine BUP drug test strips:
- 10ng sensitivity.
- Detects Buprenorphine (also known as Subutex) for up to 5 days after last use
- 99.8% accuracy
- Quick and easy to use urine drug test strip
- Read result in 3-5 minutes
- Manufactured by ALLTEST
- Full CE & international quality certified test.
- Each drug test kit is an individually foil wrapped urine drug test strip.
IgE Test (Cassette) GBR-3112
"Export use Only" Total-IgE Rapid Test is a one-step qualitative immunoassay for the detection of elevated levels of immunoglobulin E (total IgE) in human serum or plasma. This human IgE rapid test is an aid for diagnosis of allergic reactions and autoimmune disorders. Materials provided with the Total-IgE Rapid Test Kits: 1. Testing Device 2. Sample Dropper 3. Test Instructions Materials required, not provided: 1. Specimen collection container 2. Clock or timer 3. Centrifuge IgE Rapid Test Background Information An elevated concentration of IgE in serum is a common symptom associated with allergic pathologies; it may also becaused by autoimmune diseases and some infections. Rapid detection of elevated levels of IgE using the Diagnostic Automation Total- IgE Test will help in the diagnosis and treatment of IgE-mediated allergic and autoimmune disorders. IgE Rapid Test Principle The test utilizes the sandwich immunodetection principle. Dye conjugated polyclonal antibody against human IgE and immobilized mouse monoclonal anti-human IgE antibody bind to IgE in the sample specimen to produce a distinctive visual pattern registering IgE concentrations of 80 IU/ml and higher. In the test procedure, patient serum or plasma is added to the sample well "S" of the test device with the aid of a sample dropper. Labeled antibodydye conjugate binds to the human IgE molecules present in the specimen forming an antigen- antibody-dye complex. When the total IgE concentration is at or above the sensitivity level of the test, a visual test band forms in the test zone "T". For additional details please refer to the instructions for use. For a complete list of Rapid Tests, ELISA tests, IFA Kits, Serology Tests, and available testing Instrumentation, please visit our website home page or contact our Customer Service Representatives at 818-591-3030.
(AMP) Amphetamine Test (Cassette) GBR-3408
Directions for use:
- Remove the test device from its foil wrapper by tearing along the slice.
- Using the specimen dropper, withdraw urine sample from the specimen cup and slowly dispense three drops (approx 120 UI) into the circular sample well.
- Be careful not to overfill the absorbent pad.
- Read results after 5 minutes.
- For medical and other professional in vitro diagnostic use only.
- Do not use after expiration date.
- The test device should remain in the sealed pouch until use.
- The test is for single use only. Do not reuse.
- Wearing gloves is recommended.
- Store as packaged in the sealed pouch at anywhere between 2-30° (36-46°F).
- The test is stable through to the expiration date printed on the sealed pouch.
- The test must remain in the pouch until use.
- Do not freeze.
- Do not use beyond the expiration date.
- Positive: One colour line appears in the control region. No line appears in the test region.
- Negative: Two lines appear; one colour line in the control region, and another apparent colour line in the test region.
- Invalid: Control line fails to appear.
There are no reviews yet.