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Detection Principle: The double antibody sandwich ELISA method was used in this experiment. Anti mouse mip-1α The monoclonal antibody was coated on the microplate, and mip-1&alpha in samples and standards; It will bind to the antibody fixed on the plate, and the free components will be washed away; Horseradish peroxidase labeled anti mouse mip-1&alpha was added; Polyclonal antibody, and mip-1&alpha bound on the microplate; Combine to form immune complexes, and the free components are washed away; Add the substrate solution (chromogenic agent), the color of the solution gradually turns blue, add the stop solution, the solution turns yellow and stops changing. The absorbance was measured with a microplate reader. Detection Type: Double antibody sandwich method Form: pre coated 96 well plate Detection Sample Type: cell supernatant, serum, Plasma Loading Amount: 100ul Kit Components: Precoated 96 well plates, standards, anti mouse mip-1α One copy of detection antibody, dilution buffer, chromogenic solution (a, b), washing solution, termination solution, sa-hrp, plate sealing membrane and instructions. Sensitivity: 1.5 pg/ml Detection Range: 7.81 - 500 pg/ml Recovery Range: 85.0-111.9% Storage Method: 2-8 ℃ Standard CurveBackground: MIP-1 alpha (macrophage inflammatory protein 1 alpha) is a member of the CC or beta chemokine subfamily, which was initially purified from the conditioned medium of LPS stimulated murine macrophage cell lines. Mip-1& alpha; is highly effective on a variety of cells (including monocytes, T cells, B cells, and eosinophils)Plays a chemotactic role. |
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Immunohistochemistry

