11 Questions 21 Answers 0 Followers
Questions related from Heba Abdelwahab
Hello, I work with L-lysine monooxygenase, FAD is the co-factor and the enzyme is NAD(P)H dependent!one of the mutations I am studying, is oriented very close to FAD isoalloxazine moiety. it is...
05 April 2016 1,691 4 View
For my experiment, I am running an enzymatic reaction, if I need to quantify the product but I don't have a standard or extinction coefficient at a specific absorption. Can I use the decrease in...
20 January 2016 9,589 5 View
HI I was wondering if the light of UV-vis spectrophotometer can enhance the transmitted light (increase the absorption at specific wavelength of a compound when measured over time? I have this...
20 September 2015 9,890 11 View
I am working with a flavin-dependent enzyme, when I am trying to measure kinetics for the enzyme over long time using UV-spectrophotometer. I can realize that the enzyme starts to precipitate all...
06 September 2015 1,889 5 View
I was wondering what is the best way to fit the enzymatic reaction rate when I have substrate inhibition. I tried using Kaleidagraph susbtrate inhibition equation, it is showing a very good fir...
19 August 2015 9,768 12 View
If you have an enzymatic reaction with substrate inhibition and you want to get the catalytic efficiency. What is a suitable way to calculate the value and would that be a real number? Is dividing...
26 March 2015 2,519 3 View
I have an enzyme structure which utilize NADPH, FAD and amino acid. only FAD is present in the crystal structure, Is redocking important in here for validation? and when I tried to redock FAD, it...
30 September 2014 2,293 6 View
Reference(s) would be great. Thanks!
22 September 2014 5,165 11 View
Dissolving starch (soluble one) completely
23 July 2014 2,968 4 View
Is it enzymatically, or by HPLC and mass spectrometry, or are there other methods?
31 December 2013 1,590 3 View
I need the fractions as pure as possible.
09 December 2013 5,745 3 View
