MCF-7 cells were treated with PMA, TSA and DesCoA (10 nM) in the indicated combinations for four hours prior to stimulation with insulin for 10 minutes
Kaiser, Christina, James, Stephen R
Abstract
Kaiser, Christina, James, Stephen R
Abstract
Copyright information:Taken from "Acetylation of insulin receptor substrate-1 is permissive for tyrosine phosphorylation"BMC Biology 2004;2():23-23.Published online 2 Nov 2004PMCID:PMC529456.Copyright © 2004 Kaiser and James; licensee BioMed Central Ltd. IRS-1 was immunoprecipitated and western blotted for the presence of IRS-1 itself, HDAC2 and phosphotyrosine. The graph shows average data for phosphotyrosine from three independent experiments (± SEM) normalised to the response to insulin alone.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Copyright information:Taken from "Acetylation of insulin receptor substrate-1 is permissive for tyrosine phosphorylation"BMC Biology 2004;2():23-23.Published online 2 Nov 2004PMCID:PMC529456.Copyright © 2004 Kaiser and James; licensee BioMed Central Ltd. IRS-1 was immunoprecipitated and western blotted for the presence of IRS-1 itself, HDAC2 and phosphotyrosine. The graph shows average data for phosphotyrosine from three independent experiments (± SEM) normalised to the response to insulin alone.
Key concepts: Stimulation, Insulin, Medicine, Chemistry, Endocrinology, Internal medicine