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Hi all. I ran the enzyme activity (pure Tyrosinase after purification using recombinant e coli) using L-Dopa with this condition 50 mM phosphate buffer ph 6, 1mM L-Dopa 25 C temperature 0.5 mM...
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I am a bit confused about the matter. The majority of papers and explanations I have come across indicate that the inhibited line is generally positioned above the uninhibited line, but I have...
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I have done protein -protein docking using hdock server. however the interaction cannot be viewed using ligplot as shown in the attached photo. does anyone has the same experience? Thanks !
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Hi all, Im using HDOCK server to see protein-protein binding, I got the 10 best predictions and downloaded the pdb files. However when I open it to see the interaction using Ligplot, it failed and...
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Hi, I am currently calculating my ic50 using graphpad, however im confused whether to use my data from the raw data (triplicates) of each concentration or from the mean ? my ic50 is based on the...
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Im doing enzyme assay for the proteases of sars cov 2 . However with different concentrations of the protein, the solution did not change colour to yellow. Im wondering if these substrates have...
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