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Assaying protein palmitoylation in plants-4

Authors: Hemsley, Piers A; Taylor, Laura; Grierson, Claire S;

Assaying protein palmitoylation in plants-4

Abstract

Copyright information:Taken from "Assaying protein palmitoylation in plants"http://www.plantmethods.com/content/4/1/2Plant Methods 2008;4():2-2.Published online 11 Jan 2008PMCID:PMC2244627.int mutant TIP1 CA, were put through the biotin switch protocol summarised in Figure 1. Samples were treated with (Hyd+) or without (Hyd-) the thioester cleavage reagent hydroxylamine. The loading controls show that equal amounts of TIP1 and TIP1 CA were loaded onto neutravidin beads. The lanes labelled 'S-acylation' show the levels of TIP1 and TIP1 CA recovered from the neutravidin beads, and therefore originally S-acylated. TIP1 and TIP1 CA have masses of 70 kDa. The results show that Arabidopsis TIP1 binds acyl groups by a covalent thioester bond but TIP1 CA does not, consistent with previous results using a H-palmitic acid S-acylation assay [18].

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
0
Average
Average
Average