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Questions related from Madhurima Gupta
I don't have 1.5M tris HCl buffer for the resolving gel but I have 1 M tris HCl buffer with pH 8.8 will that work for SDS PAGE? do I need to change the amount added to the mix?
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i am working with lyophilised porcine skin. what tests can be carried out on the extracted sample to determine what proteins/ components are present?
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please share an easy-to-follow protocol of lowry assay, along with the method to prepare BSA standard graph in the range of 5ug/ ml to 100ug/ml
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hi, I am working on extracting proteins from pig skin. Initially, I used plain 0.5 M acetic acid solution for extracting proteins and used the solution as such post-centrifugation. but the protein...
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I am working with protein extraction using porcine skin. prior to protein extraction I need to de-fat the tissue. I am using triton x to de-fat the tissue... how to determine if the defatting is...
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