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  • FAQ: How should the Blue Loading Buffer be used?

    1.Add 1/10 volume of the 30X DTT solution to 1 volume 3X Blue Loading Buffer.
    2.Add 1/2 volume of the above mix to the protein sample.
    3.Heat at 100°C for 5 minutes to denature the protein.
    4.Spin for 30 seconds in a microfuge to remove precipitated material.
    5.Load onto gel.