The Rat follicle-stimulating hormone (FSH) ELISA Kit is designed for the quantitative determination of endogenic rat FSH concentrations in serum, plasma, or tissue homogenates. This assay employs the quantitative sandwich enzyme immunoassay technique. Antibody specific for FSH has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any FSH present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for FSH is added to the wells. After washing, avidin conjugated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of FSH bound in the initial step. The color development is stopped and the intensity of the color is measured.
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(1 mL)Includes 1 vial of negative TSH control. NOTE: These Rapid TSH Controls are not for use in diagnosing disease or illness to effect treatment, and/or cure.FOR FORENSIC/TOXICOLOGY USE ONLY.
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This Mouse FT4 ELISA Kit was designed for the quantitative measurement of Mouse FT4 protein in serum, plasma, tissue homogenates. It is a Competitive ELISA kit, its detection range is 4 pmol/L-64 pmol/L and the sensitivity is 1.08 pmol/L. One kit contains 96 wells.
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LNE CRM HbA1c 402 is a higher-order certified reference material produced by the french metrological institute LNE in compliance with ISO 17034 requirements. This Certified Reference Material LNE CRM HbA1c 402 corresponds to lyophilized human blood hemolysates and is intended for use as quality control materials for the verification of the accuracy of the reference method and routine methods used in clinical laboratories for the quantification of HbA1c in hemolysate or whole blood. Sample commutability was assessed through an extensive study involving seventeen of the most used method for the quantification of HbA1c in clinical laboratory using the difference in bias approach described in the IfCC recommendations on commutability assessment. Commutability results are reported in the certificate of analysis.
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