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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A 5-LO inhibitor (IC50 15 nM) selective for 5-LO over 12-LO and 15-LO (IC50s 500 and 300 nM respectively) inhibits A23187-induced 5-LO product formation in isolated human PMNs monocytes and whole blood (IC50s 0.5 0.45 and 1.5 UM respectively) increases survival in a mouse model of PAF-induced lethal shock at 3.5 mg/kg reduces pleural levels of LTB4 in a rat model of carrageenan-induced pleurisy
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A synthetic analog of natural AHLs that suppresses host immunity without inducing LasR inhibits the proliferation of mouse peripheral blood leukocytes by concanavalin A (EC50 9.3 M) without concurrent cytotoxicity does not induce LasR at 100 M
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