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GBR-3212 |
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AFP Whole Blood/Serum/Plasma Test (Cassette) GBR-3212
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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.
(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.
Peanut Test (Cassette) GBR-3113
Peanut ELISA Test kit
Peanut ELISA Test kit Intended Use
Peanut ELISA Kit that is an Enzyme Immunosorbent Assay for the qualitative determination of Peanut in food. The Peanut ELISA Kit is a rapid and sensitive Food Allergen ELISA Kit which is designed to provide a sensitive and convenient method for screening food samples for peanut residues. This Peanut ELISA Kit represents a highly sensitive detection system which is particularly capable of the quantification of peanut residues in cookies, cereals, ice cream, and chocolate.
Peanut ELISA Kit Components:
• Microplate: 96 wells coated with anti-peanut antibodies
• Extraction and sample dilution buffer
• Peanut Standards
• Conjugate anti- Peanut -peroxidase
• Substrate Solution
• Stop Solution
• Washing Solution
Method Principle
This Diagnostic Automation/ Cortez Diagnostics Inc. Peanut ELISA Kit is a quantitative test is based on the principle of the enzyme linked immunosorbent assay. An antibody directed against peanut proteins is bound on the surface of a microplate wells. Peanut containing samples or standards are given into the wells of the microtiter plate on the Peanut ELISA Kit. For further details please refer to complete instructions manual supplied with the product.
Background Information
Peanut belongs to the legumes, with a very high content of protein constituting about 25% of it. Many of these allergenic protein are present in relative high amounts. For this reason peanut represents one of the most important food allergens. For peanut allergic persons, hidden peanut allergens in food are a critical problem. Already very low amounts of peanuts can cause allergic reactions, which may lead to anaphylactic shock in severe cases. Because of this, peanut allergic persons must strictly avoid the consumption of peanuts or peanut containing food. Cross-contamination, mostly in consequence of the production process is often noticed. The chocolate production process is a representative example. This explains why in many cases the existence of peanut residues in foods cannot be excluded. Thus, sensitive detection systems, like this Peanut ELISA Kit, for peanut residues in foodstuffs are required.
(BAR) Barbiturates Test (Strip) GBR-3411
Barbiturates Urine Drug Test Strip is a rapid, visual, sensitive immunoassay test. The test is based on the principle of the high affinity and specific antibody and antigen reaction. It can be performed without the use of an instrument. The test utilizes a monoclonal antibody to selectively detect elevated levels of Barbiturates in urine at a cut-off level of 300ng/ml.
Specifications
• High sensitivity, simple, easy.
• Accuracy:>99%.
• CE & ISO approved.
• Specimen:Urine.
• Model No:BAR-U01D.
(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.
Gluten Test (Cassette) GBR-3111
This pack includes twelve (12) individual, single-use rapid tests that enable you to monitor your exposure to gluten. The urine test is used to determine if you have ingested larger amounts of gluten (500+ mg = 2+ bites of bread) over the previous 24 hours. These tests are compact and discreet making them ideal for either home use or when traveling.
Bladder Cancer Test (Cassette) GBR-3214
The Rapid ResponseTMÂ 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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