I found in some literature that they measure the total protein concentration according to the Bradford method. But I dont know why it is necessary.
Thanks in advance.
This is done in order to be able to control for differences in the microsome concentration between samples. The activity can then be expressed in terms of the amount of total protein in the microsome sample.
Thank you so much sir Adam B Shapiro.
What kind of problem may face without isolation ? Usually after homogenization the liver, the microsomal part is separated and used for EROD assay?
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I am now checking the PAPP substrate with PP2A at pH 8.4.
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Thank you for your kind consideration.
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