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A standard calibration for a spectrophotometric assay for lysozyme was created by diluting some initial concentrations of the reagents Tris HCl buffer, NaCl, Lysozyme and a Micrococcus lysodeikticus suspension.The final volume was 5ml.

The numbers in the calculation have become mixed up. Can you work out how consistently to drag them back into the table? There will be two numbers left over. What will these represent?

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