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Questions related from Richelle Galope
Hi all, For context, I am conducting a stability study using an ADC material formulated in different buffer systems to screen for the optimal pH/buffer to use for the final drug formulation. The...
24 November 2023 5,451 2 View
I am fairly new to ion exchange chromatography, and I am trying to optimize conditions to purify a protein having a pI value 8. I am using an anion exchanger (Q) in pH 6.0. I am aiming to separate...
11 November 2019 5,243 3 View
I am purifying a protein naturally containing His residues (the number of residues are much lesser than the His-tagged ones so binding is a bit weaker). I have previously established a...
28 March 2019 9,443 5 View
Hi! Can anyone give insights as to which of these two methods is better? We're trying to express a recombinant protein in E.coli. It is quite difficult to express this protein in its native...
06 August 2018 8,930 1 View
We expressed a recombinant protein in yeast. This protein naturally has one glycosylation site, but site-directed mutation was done to produce a non-glycosylated form since yeast is able to...
08 February 2018 4,134 2 View
Hi, can anyone share a good refolding method for TGF beta3 expressed in E.coli as inclusion bodies? We have tried using a refolding screen test kit from Pierce, but we get protein...
16 August 2017 4,497 3 View
After doing 2DGE and MALDI-MS, some of the proteins identified have lower sequence coverage values (
21 December 2016 922 7 View
I am working on a secreted protein, so my protein samples are taken from the cultured media. I wanted to check interaction of this protein with other proteins also, so I am planning to do...
25 August 2016 1,048 3 View
This question is concerned with the study about interferon response in human hepatoma cell line (Huh7). After doing proteomic analysis using ICAT and tandem mass spectrometry (MS/MS), this data is...
22 April 2015 9,042 2 View