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Home Shop REAGENTS/ASSAYS Rapid Tests CK-MB Whole Blood/Serum/Plasma Test (Cassette) GBR-3314
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CK-MB Whole Blood/Serum/Plasma Test (Cassette) GBR-3314

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Сatalog number: GBR-3314 Category: Rapid Tests
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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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AFP Serum Test (Strip 5mm) GBR-3211

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(BZO) Benzodiazepine Test (Cassette) GBR-3412

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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.  
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Myoglobin Whole Blood/Serum/Plasma Test (Cassette) GBR-3315

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IgE Test (Cassette) GBR-3112

Rapid Tests, ALLERGY TESTS
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"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.
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(AMP) Amphetamine Test (Strip) GBR-3409

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Directions for use:
      1. Remove the strip from it's packaging.
      2. Immerse the strip into the urine with the arrow end pointing towards the urine. DO NOT cover the urine over the MAX (maximum) line.
      3. Take the strip out of the urine after approximately 15 seconds, and lay it on a flat, non-absorptive clean surface.
      4. Read results after waiting 5 minutes.
DO NOT INTERPRET RESULTS AFTER 10 MINUTES   Precautions:
      • 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.
  Storage and Stability:
      • 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.
  Results:
      • 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.
  This Amphetamine (AMP) Rapid Strip Test is 98% accurate.
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AFP Serum Test (Cassette) GBR-3210

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Peanut Test (Cassette) GBR-3113

Rapid Tests, ALLERGY TESTS
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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.
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