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dc.contributor.authorJones, David R
dc.contributor.authorRamirez, I
dc.contributor.authorLowe, M
dc.contributor.authorDivecha, Nullin
dc.date.accessioned2013-06-14T15:18:56Z
dc.date.available2013-06-14T15:18:56Z
dc.date.issued2013-05-09
dc.identifier.citationMeasurement of phosphoinositides in the zebrafish Danio rerio. 2013, 8 (6):1058-72 Nat Protocen_GB
dc.identifier.issn1750-2799
dc.identifier.pmid23660755
dc.identifier.doi10.1038/nprot.2013.040
dc.identifier.urihttp://hdl.handle.net/10541/294008
dc.description.abstractPhosphoinositides represent a minor fraction of the total glycerolipids in cells. Despite the fact that phosphoinositides are present in small quantities, they have crucial roles during cell signaling and in regulating numerous intracellular processes. Measuring changes in the levels of different phosphoinositides in animals is difficult, but it is essential in order to define the important functions of specific members of the phosphoinositide family. Here we detail procedures for measuring phosphoinositides in 2-days-postfertilization (2-d.p.f.) embryos in zebrafish (Danio rerio). Both in vivo radiolabeling (using [(32)P]orthophosphate) followed by thin-layer or high-performance liquid chromatography (TLC or HPLC) analysis and specific in vitro phosphorylation assays (using [(32)P]γATP) permit the quantitative measurement of phosphoinositides. Normalization of both measurements can be achieved by the determination of total lipid phosphate in embryos. All the techniques described are relatively inexpensive and accessible to most laboratories with an interest in studying the effect of gene manipulation on phosphoinositide metabolism in zebrafish. All the procedures described herein will take up to 10 working days.
dc.language.isoenen
dc.rightsArchived with thanks to Nature protocolsen_GB
dc.titleMeasurement of phosphoinositides in the zebrafish Danio rerio.en
dc.typeArticleen
dc.contributor.departmentCancer Research UK Inositide Laboratory, Paterson Institute for Cancer Research, University of Manchester, Manchester, UK.en_GB
dc.identifier.journalNature Protocolsen_GB
html.description.abstractPhosphoinositides represent a minor fraction of the total glycerolipids in cells. Despite the fact that phosphoinositides are present in small quantities, they have crucial roles during cell signaling and in regulating numerous intracellular processes. Measuring changes in the levels of different phosphoinositides in animals is difficult, but it is essential in order to define the important functions of specific members of the phosphoinositide family. Here we detail procedures for measuring phosphoinositides in 2-days-postfertilization (2-d.p.f.) embryos in zebrafish (Danio rerio). Both in vivo radiolabeling (using [(32)P]orthophosphate) followed by thin-layer or high-performance liquid chromatography (TLC or HPLC) analysis and specific in vitro phosphorylation assays (using [(32)P]γATP) permit the quantitative measurement of phosphoinositides. Normalization of both measurements can be achieved by the determination of total lipid phosphate in embryos. All the techniques described are relatively inexpensive and accessible to most laboratories with an interest in studying the effect of gene manipulation on phosphoinositide metabolism in zebrafish. All the procedures described herein will take up to 10 working days.


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