| CAT NO. |
GBR-3415 |
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(BUP) Buprenorphine Test (Strip) GBR-3415
ALLTEST Buprenorphine BUP urine drug testing strips
Key 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.
Additional information
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(AMP) Amphetamine Test (Cassette) GBR-3408
Directions for use:
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- 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.
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- 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.
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-
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- 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.
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- 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.
(BZO) Benzodiazepine Test (Cassette) GBR-3412
Note:Could be customized under your request
Specifications
1. High sensitivity, simple, easy.
2. Accuracy: >99%.
3. CE & ISO approved.
4. Specimen: Urine.
5. Model No:BZO-U02D
1.Application
The BZO Rapid Test Device (Urine) detects Benzodiazepines through visual interpretation of color development
on the Device. Drug conjugates are immobilized on the test region of the membrane. During testing, the specimen
reacts with antibodies conjugated to colored particles and precoated on the sample pad. The mixture then
migratesthrough the membrane by capillary action, and interacts with reagents on the membrane. If there are
insufficient drug molecules in the specimen, the antibody-colored particle conjugate will bind to the drug conjugates,
forming a colored band at the test region of the membrane. Therefore, a colored band appears in the test region
when the urine is negative for the drug. If drug molecules are present in the urine above the cut-off concentration
of the test, they compete with the immobilized drug conjugate on the test region for limited antibody binding sites.
This will prevent attachment of the antibody-colored particle conjugate to the test region. Therefore, the absence
of a colored band at the test region indicates a positive result. The appearance of a colored band at the control
region serves as a procedural control, indicating that the proper volume of specimen has been added and
membrane wicking has occurred.
2. Usage:
Allow test device,urine specimen,and/or controls to equilibrate to room temperature (15-30°C) prior to testing.
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 (Strip) GBR-3409
Directions for use:
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- Remove the strip from it's packaging.
- Immerse the strip into the urine with the arrow end pointing towards the urine. DO NOT cover the urine over the MAX (maximum) line.
- Take the strip out of the urine after approximately 15 seconds, and lay it on a flat, non-absorptive clean surface.
- Read results after waiting 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.
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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).
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