I performed the multiplex cytokine bead array (Thermofisher Procartaplex 20 plex) for plasma samples. However, I forgot to mix the contents while loading the standard 1 in the first well (A1) of the 96-well plate. Due to this, the standard curve formed is a bit deviated because of the standard concentration value of A1. I have attached the image of the standard curve formed. Please suggest how do I analyze the data.

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