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H. Pylori Test Kit TechLab H. Pylori Chek T5051, Enzyme Immunoassay (EIA

H. Pylori Test Kit TechLab H. Pylori Chek T5051, Enzyme Immunoassay (EIA

CAUTION: NON RETURNABLE
CAUTION: EXPIRY ARE ALWAYS 90 Days or Longer, DO NOT OVER BUY

Item#: Tech-T5051-KT
$2,856.32
Item(s) Total: $2,856.32
H. Pylori Test Kit TechLab H. Pylori Chek T5051, Enzyme Immunoassay (EIA), Contents Include: 7 mL Conjugate, 40 mL Diluent, 7 mL Stop Solution, 3.5 mL Positive Control, 14 mL Substrate, 50 mL Wash Buffer Concentrate, 12 Strip Microassay Plate, (100) Transfer Pipettes, (2) Plastic Adhesive Sheets, Wash Solution Label, (50) Wooden Applicator Sticks, SOLD AS 96/Kit

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  • Product Details
    • Dealer # 1198017
    Manufacturer # T5051
    Brand TechLab® H. Pylori Chek™
    Manufacturer TECHLAB Inc
    Country of Origin United States
    Application H. Pylori Test Kit
    CLIA Classified CLIA Non-Waived
    Contents 1 7 mL Conjugate, 40 mL Diluent, 7 mL Stop Solution, 3.5 mL Positive Control, 14 mL Substrate, 50 mL Wash Buffer Concentrate, 12 Strip Microassay Plate, (100) Transfer Pipettes, (2) Plastic Adhesive Sheets, Wash Solution Label, (50) Wooden Applicator Sticks
    For Use With For ELISA Reader capable of Reading at 450 nm, 450 / 620 nm or 450 / 630 nm
    Number of Tests 96 Tests
    Reading Type Machine Read
    Sample Type Stool Sample
    Specialty Immunoassay
    Storage Requirements Requires Refrigeration
    Test Format Microwell Format
    Test Kit Type Standard
    Test Name H. Pylori
    Test Type Enzyme Immunoassay (EIA)
    Time to Results 60 Minute Results
    UNSPSC Code 41116129

    Features

    • The H. PYLORI CHEK™ test is an enzyme immunoassay for the qualitative detection of Helicobacter pylori specific antigen in human fecal specimens
    • It is a noninvasive way to detect H. pylori when endoscopy is not required, using antibodies specific to H. pylori antigen
    • The test is intended for use with fecal specimens that are fresh, frozen, or in transport media
    • Results in approximately 60 minutes
    • Results should be considered in conjunction with clinical findings and patient history
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