My boss has given me the purified extracellular portion of the Notch receptor. As Delta/Notch signaling occurs between cells, I know that both the Notch receptor and and Delta are most likely "comfortable" in the environment of the blood, not the cytosol, nucleus, mitochondria, etc... I want to purify Delta, the signal. What would be true of the most specific purification technique I could choose, i.e. the technique that will result in the fewest proteins in the fraction containing Delta? Do not worry about whether the protein works after fractionation yet. Pick ALL that apply. I would use ion exchange chromatography. I would use size exclusion chromatography I would use affinity chromatography I would use a water based mobile phase of 7.4 I would use an acetonitrile mobile phase with a pH of 7.4 I would use a water based mobile phase of pH 7.2 I would use an acetonitrile phase of 7.2 I would salt it out. I would obtain my soluble protein fraction by dialysis. I would obtain my soluble protein fraction by eluting from the column in stages slowly changing the pH.
My boss has given me the purified extracellular portion of the Notch receptor. As Delta/Notch signaling occurs between cells, I know that both the Notch receptor and and Delta are most likely "comfortable" in the environment of the blood, not the cytosol, nucleus, mitochondria, etc... I want to purify Delta, the signal. What would be true of the most specific purification technique I could choose, i.e. the technique that will result in the fewest proteins in the fraction containing Delta? Do not worry about whether the protein works after fractionation yet. Pick ALL that apply. I would use ion exchange chromatography. I would use size exclusion chromatography I would use affinity chromatography I would use a water based mobile phase of 7.4 I would use an acetonitrile mobile phase with a pH of 7.4 I would use a water based mobile phase of pH 7.2 I would use an acetonitrile phase of 7.2 I would salt it out. I would obtain my soluble protein fraction by dialysis. I would obtain my soluble protein fraction by eluting from the column in stages slowly changing the pH.
Human Anatomy & Physiology (11th Edition)
11th Edition
ISBN:9780134580999
Author:Elaine N. Marieb, Katja N. Hoehn
Publisher:Elaine N. Marieb, Katja N. Hoehn
Chapter1: The Human Body: An Orientation
Section: Chapter Questions
Problem 1RQ: The correct sequence of levels forming the structural hierarchy is A. (a) organ, organ system,...
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My boss has given me the purified extracellular portion of the Notch receptor. As Delta/Notch signaling occurs between cells, I know that both the Notch receptor and and Delta are most likely "comfortable" in the environment of the blood, not the cytosol, nucleus, mitochondria, etc... I want to purify Delta, the signal. What would be true of the most specific purification technique I could choose, i.e. the technique that will result in the fewest proteins in the fraction containing Delta? Do not worry about whether the protein works after fractionation yet. Pick ALL that apply.
I would use ion exchange chromatography.
I would use size exclusion chromatography
I would use affinity chromatography
I would use a water based mobile phase of 7.4
I would use an acetonitrile mobile phase with a pH of 7.4
I would use a water based mobile phase of pH 7.2
I would use an acetonitrile phase of 7.2
I would salt it out.
I would obtain my soluble protein fraction by dialysis.
I would obtain my soluble protein fraction by eluting from the column in stages slowly changing the pH.
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