PMC:3589482 / 13849-14836
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Transfected cells were transferred to pre-warmed media in 24 well plates and incubated for 48 hrs prior to incubation with LPS (100 ng/ml) for 4 hrs where indicated. In some experiments, plasmids encoding C/EBP-β or C/EBP-β phospho-acceptor mutants (T188A, T217A, S64A) [38]–[40] or control vector were co-transfected (0.6–1.0 µg total DNA). Luciferase activity was determined and normalized to that of β-galactosidase [38] using the Luciferase Assay System and β-Galactosidase Enzyme Assay System Kits, respectively (Promega). Each experiment was repeated at least three times, and triplicate samples were employed for each sample. Expression of the C/EBP-β phospho-acceptor mutant proteins was checked for equal expression by western blot.\n"}
2_test
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bionlp-st-ge-2016-test-proteins
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bionlp-st-ge-2016-uniprot
{"project":"bionlp-st-ge-2016-uniprot","denotations":[{"id":"T7497","span":{"begin":114,"end":121},"obj":"http://www.uniprot.org/uniprot/P60709"},{"id":"T7496","span":{"begin":896,"end":903},"obj":"http://www.uniprot.org/uniprot/P28033"},{"id":"T7495","span":{"begin":461,"end":468},"obj":"http://www.uniprot.org/uniprot/P28033"},{"id":"T7494","span":{"begin":450,"end":457},"obj":"http://www.uniprot.org/uniprot/P28033"},{"id":"T7493","span":{"begin":0,"end":5},"obj":"http://www.uniprot.org/uniprot/P28033"},{"id":"T7492","span":{"begin":679,"end":689},"obj":"http://www.uniprot.org/uniprot/P08659"},{"id":"T7491","span":{"begin":587,"end":597},"obj":"http://www.uniprot.org/uniprot/P08659"}],"namespaces":[{"prefix":"_base","uri":"http://www.uniprot.org/uniprot/"}],"text":"Cebpb −/− MEFs (1×105) [34] were transfected with the indicated luciferase reporter plasmid (400 ng) along with a β-actin-β-galactosidase reporter plasmid (200 ng) by electroporation using the Invitrogen Neon™ system (1 pulse, 1350 V, 30 msec). Transfected cells were transferred to pre-warmed media in 24 well plates and incubated for 48 hrs prior to incubation with LPS (100 ng/ml) for 4 hrs where indicated. In some experiments, plasmids encoding C/EBP-β or C/EBP-β phospho-acceptor mutants (T188A, T217A, S64A) [38]–[40] or control vector were co-transfected (0.6–1.0 µg total DNA). Luciferase activity was determined and normalized to that of β-galactosidase [38] using the Luciferase Assay System and β-Galactosidase Enzyme Assay System Kits, respectively (Promega). Each experiment was repeated at least three times, and triplicate samples were employed for each sample. Expression of the C/EBP-β phospho-acceptor mutant proteins was checked for equal expression by western blot.\n"}
GO-BP
{"project":"GO-BP","denotations":[{"id":"T7252","span":{"begin":587,"end":606},"obj":"http://purl.obolibrary.org/obo/GO_0050397"},{"id":"T7251","span":{"begin":587,"end":606},"obj":"http://purl.obolibrary.org/obo/GO_0050248"},{"id":"T7250","span":{"begin":587,"end":606},"obj":"http://purl.obolibrary.org/obo/GO_0047712"},{"id":"T7249","span":{"begin":587,"end":606},"obj":"http://purl.obolibrary.org/obo/GO_0047077"},{"id":"T7248","span":{"begin":587,"end":606},"obj":"http://purl.obolibrary.org/obo/GO_0045289"}],"text":"Cebpb −/− MEFs (1×105) [34] were transfected with the indicated luciferase reporter plasmid (400 ng) along with a β-actin-β-galactosidase reporter plasmid (200 ng) by electroporation using the Invitrogen Neon™ system (1 pulse, 1350 V, 30 msec). Transfected cells were transferred to pre-warmed media in 24 well plates and incubated for 48 hrs prior to incubation with LPS (100 ng/ml) for 4 hrs where indicated. In some experiments, plasmids encoding C/EBP-β or C/EBP-β phospho-acceptor mutants (T188A, T217A, S64A) [38]–[40] or control vector were co-transfected (0.6–1.0 µg total DNA). Luciferase activity was determined and normalized to that of β-galactosidase [38] using the Luciferase Assay System and β-Galactosidase Enzyme Assay System Kits, respectively (Promega). Each experiment was repeated at least three times, and triplicate samples were employed for each sample. Expression of the C/EBP-β phospho-acceptor mutant proteins was checked for equal expression by western blot.\n"}
GO-MF
{"project":"GO-MF","denotations":[{"id":"T7257","span":{"begin":587,"end":606},"obj":"http://purl.obolibrary.org/obo/GO_0050397"},{"id":"T7256","span":{"begin":587,"end":606},"obj":"http://purl.obolibrary.org/obo/GO_0050248"},{"id":"T7255","span":{"begin":587,"end":606},"obj":"http://purl.obolibrary.org/obo/GO_0047712"},{"id":"T7254","span":{"begin":587,"end":606},"obj":"http://purl.obolibrary.org/obo/GO_0047077"},{"id":"T7253","span":{"begin":587,"end":606},"obj":"http://purl.obolibrary.org/obo/GO_0045289"}],"text":"Cebpb −/− MEFs (1×105) [34] were transfected with the indicated luciferase reporter plasmid (400 ng) along with a β-actin-β-galactosidase reporter plasmid (200 ng) by electroporation using the Invitrogen Neon™ system (1 pulse, 1350 V, 30 msec). Transfected cells were transferred to pre-warmed media in 24 well plates and incubated for 48 hrs prior to incubation with LPS (100 ng/ml) for 4 hrs where indicated. In some experiments, plasmids encoding C/EBP-β or C/EBP-β phospho-acceptor mutants (T188A, T217A, S64A) [38]–[40] or control vector were co-transfected (0.6–1.0 µg total DNA). Luciferase activity was determined and normalized to that of β-galactosidase [38] using the Luciferase Assay System and β-Galactosidase Enzyme Assay System Kits, respectively (Promega). Each experiment was repeated at least three times, and triplicate samples were employed for each sample. Expression of the C/EBP-β phospho-acceptor mutant proteins was checked for equal expression by western blot.\n"}
GO-CC
{"project":"GO-CC","denotations":[{"id":"T7258","span":{"begin":257,"end":262},"obj":"http://purl.obolibrary.org/obo/GO_0005623"}],"text":"Cebpb −/− MEFs (1×105) [34] were transfected with the indicated luciferase reporter plasmid (400 ng) along with a β-actin-β-galactosidase reporter plasmid (200 ng) by electroporation using the Invitrogen Neon™ system (1 pulse, 1350 V, 30 msec). Transfected cells were transferred to pre-warmed media in 24 well plates and incubated for 48 hrs prior to incubation with LPS (100 ng/ml) for 4 hrs where indicated. In some experiments, plasmids encoding C/EBP-β or C/EBP-β phospho-acceptor mutants (T188A, T217A, S64A) [38]–[40] or control vector were co-transfected (0.6–1.0 µg total DNA). Luciferase activity was determined and normalized to that of β-galactosidase [38] using the Luciferase Assay System and β-Galactosidase Enzyme Assay System Kits, respectively (Promega). Each experiment was repeated at least three times, and triplicate samples were employed for each sample. Expression of the C/EBP-β phospho-acceptor mutant proteins was checked for equal expression by western blot.\n"}
sentences
{"project":"sentences","denotations":[{"id":"T7216","span":{"begin":878,"end":986},"obj":"Sentence"},{"id":"T7215","span":{"begin":773,"end":877},"obj":"Sentence"},{"id":"T7214","span":{"begin":587,"end":772},"obj":"Sentence"},{"id":"T7213","span":{"begin":411,"end":586},"obj":"Sentence"},{"id":"T7212","span":{"begin":245,"end":410},"obj":"Sentence"},{"id":"T7211","span":{"begin":0,"end":244},"obj":"Sentence"},{"id":"T85","span":{"begin":0,"end":244},"obj":"Sentence"},{"id":"T86","span":{"begin":245,"end":410},"obj":"Sentence"},{"id":"T87","span":{"begin":411,"end":586},"obj":"Sentence"},{"id":"T88","span":{"begin":587,"end":772},"obj":"Sentence"},{"id":"T89","span":{"begin":773,"end":877},"obj":"Sentence"},{"id":"T90","span":{"begin":878,"end":986},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"Cebpb −/− MEFs (1×105) [34] were transfected with the indicated luciferase reporter plasmid (400 ng) along with a β-actin-β-galactosidase reporter plasmid (200 ng) by electroporation using the Invitrogen Neon™ system (1 pulse, 1350 V, 30 msec). Transfected cells were transferred to pre-warmed media in 24 well plates and incubated for 48 hrs prior to incubation with LPS (100 ng/ml) for 4 hrs where indicated. In some experiments, plasmids encoding C/EBP-β or C/EBP-β phospho-acceptor mutants (T188A, T217A, S64A) [38]–[40] or control vector were co-transfected (0.6–1.0 µg total DNA). Luciferase activity was determined and normalized to that of β-galactosidase [38] using the Luciferase Assay System and β-Galactosidase Enzyme Assay System Kits, respectively (Promega). Each experiment was repeated at least three times, and triplicate samples were employed for each sample. Expression of the C/EBP-β phospho-acceptor mutant proteins was checked for equal expression by western blot.\n"}
simple1
{"project":"simple1","denotations":[{"id":"T7273","span":{"begin":896,"end":927},"obj":"Protein"},{"id":"T7272","span":{"begin":707,"end":722},"obj":"Protein"},{"id":"T7271","span":{"begin":679,"end":689},"obj":"Protein"},{"id":"T7270","span":{"begin":648,"end":663},"obj":"Protein"},{"id":"T7269","span":{"begin":587,"end":597},"obj":"Protein"},{"id":"T7268","span":{"begin":509,"end":513},"obj":"Protein"},{"id":"T7267","span":{"begin":502,"end":507},"obj":"Protein"},{"id":"T7266","span":{"begin":495,"end":500},"obj":"Protein"},{"id":"T7265","span":{"begin":461,"end":493},"obj":"Protein"},{"id":"T7264","span":{"begin":450,"end":457},"obj":"Protein"},{"id":"T7263","span":{"begin":122,"end":137},"obj":"Protein"},{"id":"T7262","span":{"begin":114,"end":121},"obj":"Protein"},{"id":"T7261","span":{"begin":64,"end":74},"obj":"Protein"},{"id":"T7260","span":{"begin":0,"end":5},"obj":"Protein"}],"text":"Cebpb −/− MEFs (1×105) [34] were transfected with the indicated luciferase reporter plasmid (400 ng) along with a β-actin-β-galactosidase reporter plasmid (200 ng) by electroporation using the Invitrogen Neon™ system (1 pulse, 1350 V, 30 msec). Transfected cells were transferred to pre-warmed media in 24 well plates and incubated for 48 hrs prior to incubation with LPS (100 ng/ml) for 4 hrs where indicated. In some experiments, plasmids encoding C/EBP-β or C/EBP-β phospho-acceptor mutants (T188A, T217A, S64A) [38]–[40] or control vector were co-transfected (0.6–1.0 µg total DNA). Luciferase activity was determined and normalized to that of β-galactosidase [38] using the Luciferase Assay System and β-Galactosidase Enzyme Assay System Kits, respectively (Promega). Each experiment was repeated at least three times, and triplicate samples were employed for each sample. Expression of the C/EBP-β phospho-acceptor mutant proteins was checked for equal expression by western blot.\n"}
BioNLP16_DUT
{"project":"BioNLP16_DUT","denotations":[{"id":"T7489","span":{"begin":878,"end":888},"obj":"Gene_expression"},{"id":"T7488","span":{"begin":548,"end":562},"obj":"Gene_expression"},{"id":"T7487","span":{"begin":33,"end":44},"obj":"Gene_expression"},{"id":"T7486","span":{"begin":896,"end":927},"obj":"Protein"},{"id":"T7485","span":{"begin":707,"end":722},"obj":"Protein"},{"id":"T7484","span":{"begin":679,"end":689},"obj":"Protein"},{"id":"T7483","span":{"begin":648,"end":663},"obj":"Protein"},{"id":"T7482","span":{"begin":587,"end":597},"obj":"Protein"},{"id":"T7481","span":{"begin":502,"end":507},"obj":"Protein"},{"id":"T7480","span":{"begin":495,"end":500},"obj":"Protein"},{"id":"T7479","span":{"begin":461,"end":493},"obj":"Protein"},{"id":"T7478","span":{"begin":450,"end":457},"obj":"Protein"},{"id":"T7477","span":{"begin":509,"end":513},"obj":"Protein"},{"id":"T7476","span":{"begin":122,"end":137},"obj":"Protein"},{"id":"T7475","span":{"begin":114,"end":121},"obj":"Protein"},{"id":"T7474","span":{"begin":64,"end":74},"obj":"Protein"},{"id":"T7473","span":{"begin":0,"end":5},"obj":"Protein"}],"relations":[{"id":"R5379","pred":"themeOf","subj":"T7473","obj":"T7487"},{"id":"R5380","pred":"themeOf","subj":"T7474","obj":"T7487"},{"id":"R5381","pred":"themeOf","subj":"T7476","obj":"T7487"},{"id":"R5382","pred":"themeOf","subj":"T7477","obj":"T7488"},{"id":"R5383","pred":"themeOf","subj":"T7481","obj":"T7488"},{"id":"R5384","pred":"themeOf","subj":"T7486","obj":"T7489"}],"text":"Cebpb −/− MEFs (1×105) [34] were transfected with the indicated luciferase reporter plasmid (400 ng) along with a β-actin-β-galactosidase reporter plasmid (200 ng) by electroporation using the Invitrogen Neon™ system (1 pulse, 1350 V, 30 msec). Transfected cells were transferred to pre-warmed media in 24 well plates and incubated for 48 hrs prior to incubation with LPS (100 ng/ml) for 4 hrs where indicated. In some experiments, plasmids encoding C/EBP-β or C/EBP-β phospho-acceptor mutants (T188A, T217A, S64A) [38]–[40] or control vector were co-transfected (0.6–1.0 µg total DNA). Luciferase activity was determined and normalized to that of β-galactosidase [38] using the Luciferase Assay System and β-Galactosidase Enzyme Assay System Kits, respectively (Promega). Each experiment was repeated at least three times, and triplicate samples were employed for each sample. Expression of the C/EBP-β phospho-acceptor mutant proteins was checked for equal expression by western blot.\n"}
BioNLP16_Messiy
{"project":"BioNLP16_Messiy","denotations":[{"id":"T7538","span":{"begin":461,"end":493},"obj":"Protein"},{"id":"T7537","span":{"begin":450,"end":457},"obj":"Protein"},{"id":"T7536","span":{"begin":509,"end":513},"obj":"Protein"},{"id":"T7547","span":{"begin":548,"end":562},"obj":"Gene_expression"},{"id":"T7546","span":{"begin":33,"end":44},"obj":"Gene_expression"},{"id":"T7545","span":{"begin":896,"end":927},"obj":"Protein"},{"id":"T7544","span":{"begin":707,"end":722},"obj":"Protein"},{"id":"T7543","span":{"begin":679,"end":689},"obj":"Protein"},{"id":"T7542","span":{"begin":648,"end":663},"obj":"Protein"},{"id":"T7541","span":{"begin":587,"end":597},"obj":"Protein"},{"id":"T7540","span":{"begin":502,"end":507},"obj":"Protein"},{"id":"T7539","span":{"begin":495,"end":500},"obj":"Protein"},{"id":"T7535","span":{"begin":122,"end":137},"obj":"Protein"},{"id":"T7534","span":{"begin":114,"end":121},"obj":"Protein"},{"id":"T7533","span":{"begin":64,"end":74},"obj":"Protein"},{"id":"T7532","span":{"begin":0,"end":5},"obj":"Protein"},{"id":"T7548","span":{"begin":878,"end":888},"obj":"Gene_expression"}],"relations":[{"id":"R5392","pred":"themeOf","subj":"T7532","obj":"T7546"},{"id":"R5393","pred":"themeOf","subj":"T7536","obj":"T7547"},{"id":"R5394","pred":"themeOf","subj":"T7537","obj":"T7547"},{"id":"R5395","pred":"themeOf","subj":"T7539","obj":"T7547"},{"id":"R5396","pred":"themeOf","subj":"T7540","obj":"T7547"},{"id":"R5397","pred":"themeOf","subj":"T7545","obj":"T7548"}],"text":"Cebpb −/− MEFs (1×105) [34] were transfected with the indicated luciferase reporter plasmid (400 ng) along with a β-actin-β-galactosidase reporter plasmid (200 ng) by electroporation using the Invitrogen Neon™ system (1 pulse, 1350 V, 30 msec). Transfected cells were transferred to pre-warmed media in 24 well plates and incubated for 48 hrs prior to incubation with LPS (100 ng/ml) for 4 hrs where indicated. In some experiments, plasmids encoding C/EBP-β or C/EBP-β phospho-acceptor mutants (T188A, T217A, S64A) [38]–[40] or control vector were co-transfected (0.6–1.0 µg total DNA). Luciferase activity was determined and normalized to that of β-galactosidase [38] using the Luciferase Assay System and β-Galactosidase Enzyme Assay System Kits, respectively (Promega). Each experiment was repeated at least three times, and triplicate samples were employed for each sample. Expression of the C/EBP-β phospho-acceptor mutant proteins was checked for equal expression by western blot.\n"}
DLUT931
{"project":"DLUT931","denotations":[{"id":"T7514","span":{"begin":878,"end":888},"obj":"Gene_expression"},{"id":"T7513","span":{"begin":548,"end":562},"obj":"Gene_expression"},{"id":"T7512","span":{"begin":896,"end":927},"obj":"Protein"},{"id":"T7511","span":{"begin":707,"end":722},"obj":"Protein"},{"id":"T7510","span":{"begin":679,"end":689},"obj":"Protein"},{"id":"T7509","span":{"begin":648,"end":663},"obj":"Protein"},{"id":"T7508","span":{"begin":587,"end":597},"obj":"Protein"},{"id":"T7507","span":{"begin":502,"end":507},"obj":"Protein"},{"id":"T7506","span":{"begin":495,"end":500},"obj":"Protein"},{"id":"T7505","span":{"begin":461,"end":493},"obj":"Protein"},{"id":"T7504","span":{"begin":450,"end":457},"obj":"Protein"},{"id":"T7503","span":{"begin":509,"end":513},"obj":"Protein"},{"id":"T7502","span":{"begin":122,"end":137},"obj":"Protein"},{"id":"T7501","span":{"begin":114,"end":121},"obj":"Protein"},{"id":"T7500","span":{"begin":64,"end":74},"obj":"Protein"},{"id":"T7499","span":{"begin":0,"end":5},"obj":"Protein"}],"relations":[{"id":"R5385","pred":"themeOf","subj":"T7503","obj":"T7513"},{"id":"R5386","pred":"themeOf","subj":"T7504","obj":"T7513"},{"id":"R5387","pred":"themeOf","subj":"T7505","obj":"T7513"},{"id":"R5388","pred":"themeOf","subj":"T7506","obj":"T7513"},{"id":"R5389","pred":"themeOf","subj":"T7507","obj":"T7513"},{"id":"R5390","pred":"themeOf","subj":"T7512","obj":"T7514"}],"text":"Cebpb −/− MEFs (1×105) [34] were transfected with the indicated luciferase reporter plasmid (400 ng) along with a β-actin-β-galactosidase reporter plasmid (200 ng) by electroporation using the Invitrogen Neon™ system (1 pulse, 1350 V, 30 msec). Transfected cells were transferred to pre-warmed media in 24 well plates and incubated for 48 hrs prior to incubation with LPS (100 ng/ml) for 4 hrs where indicated. In some experiments, plasmids encoding C/EBP-β or C/EBP-β phospho-acceptor mutants (T188A, T217A, S64A) [38]–[40] or control vector were co-transfected (0.6–1.0 µg total DNA). Luciferase activity was determined and normalized to that of β-galactosidase [38] using the Luciferase Assay System and β-Galactosidase Enzyme Assay System Kits, respectively (Promega). Each experiment was repeated at least three times, and triplicate samples were employed for each sample. Expression of the C/EBP-β phospho-acceptor mutant proteins was checked for equal expression by western blot.\n"}
bionlp-st-ge-2016-test-ihmc
{"project":"bionlp-st-ge-2016-test-ihmc","denotations":[{"id":"T7596","span":{"begin":878,"end":936},"obj":"Gene_expression"},{"id":"T7594","span":{"begin":112,"end":154},"obj":"Protein"},{"id":"T7593","span":{"begin":648,"end":668},"obj":"Protein"},{"id":"T7592","span":{"begin":64,"end":74},"obj":"Protein"},{"id":"T7591","span":{"begin":388,"end":393},"obj":"Protein"},{"id":"T7590","span":{"begin":679,"end":689},"obj":"Protein"},{"id":"T7589","span":{"begin":581,"end":584},"obj":"Entity"},{"id":"T7588","span":{"begin":112,"end":154},"obj":"Protein"},{"id":"T7587","span":{"begin":495,"end":513},"obj":"Protein"},{"id":"T7586","span":{"begin":368,"end":371},"obj":"Entity"},{"id":"T7585","span":{"begin":587,"end":610},"obj":"Protein"},{"id":"T7584","span":{"begin":10,"end":22},"obj":"Protein"},{"id":"T7583","span":{"begin":707,"end":747},"obj":"Protein"},{"id":"T7582","span":{"begin":502,"end":507},"obj":"Protein"},{"id":"T7581","span":{"begin":896,"end":927},"obj":"Protein"},{"id":"T7580","span":{"begin":707,"end":747},"obj":"Protein"},{"id":"T7579","span":{"begin":707,"end":722},"obj":"Protein"},{"id":"T7578","span":{"begin":495,"end":508},"obj":"Protein"},{"id":"T7577","span":{"begin":450,"end":457},"obj":"Protein"},{"id":"T7576","span":{"begin":461,"end":514},"obj":"Protein"},{"id":"T7575","span":{"begin":889,"end":936},"obj":"Protein"}],"relations":[{"id":"R5402","pred":"themeOf","subj":"T7575","obj":"T7596"}],"text":"Cebpb −/− MEFs (1×105) [34] were transfected with the indicated luciferase reporter plasmid (400 ng) along with a β-actin-β-galactosidase reporter plasmid (200 ng) by electroporation using the Invitrogen Neon™ system (1 pulse, 1350 V, 30 msec). Transfected cells were transferred to pre-warmed media in 24 well plates and incubated for 48 hrs prior to incubation with LPS (100 ng/ml) for 4 hrs where indicated. In some experiments, plasmids encoding C/EBP-β or C/EBP-β phospho-acceptor mutants (T188A, T217A, S64A) [38]–[40] or control vector were co-transfected (0.6–1.0 µg total DNA). Luciferase activity was determined and normalized to that of β-galactosidase [38] using the Luciferase Assay System and β-Galactosidase Enzyme Assay System Kits, respectively (Promega). Each experiment was repeated at least three times, and triplicate samples were employed for each sample. Expression of the C/EBP-β phospho-acceptor mutant proteins was checked for equal expression by western blot.\n"}
bionlp-st-ge-2016-test-tees
{"project":"bionlp-st-ge-2016-test-tees","denotations":[{"id":"T7561","span":{"begin":941,"end":948},"obj":"Positive_regulation"},{"id":"T7560","span":{"begin":878,"end":888},"obj":"Gene_expression"},{"id":"T7559","span":{"begin":896,"end":936},"obj":"Protein"},{"id":"T7558","span":{"begin":707,"end":729},"obj":"Protein"},{"id":"T7557","span":{"begin":696,"end":702},"obj":"Protein"},{"id":"T7556","span":{"begin":679,"end":689},"obj":"Protein"},{"id":"T7555","span":{"begin":648,"end":663},"obj":"Protein"},{"id":"T7554","span":{"begin":587,"end":597},"obj":"Protein"},{"id":"T7553","span":{"begin":461,"end":468},"obj":"Protein"},{"id":"T7552","span":{"begin":450,"end":457},"obj":"Protein"},{"id":"T7551","span":{"begin":114,"end":146},"obj":"Protein"},{"id":"T7550","span":{"begin":64,"end":74},"obj":"Protein"}],"relations":[{"id":"R5398","pred":"themeOf","subj":"T7559","obj":"T7560"},{"id":"R5399","pred":"themeOf","subj":"T7560","obj":"T7561"}],"text":"Cebpb −/− MEFs (1×105) [34] were transfected with the indicated luciferase reporter plasmid (400 ng) along with a β-actin-β-galactosidase reporter plasmid (200 ng) by electroporation using the Invitrogen Neon™ system (1 pulse, 1350 V, 30 msec). Transfected cells were transferred to pre-warmed media in 24 well plates and incubated for 48 hrs prior to incubation with LPS (100 ng/ml) for 4 hrs where indicated. In some experiments, plasmids encoding C/EBP-β or C/EBP-β phospho-acceptor mutants (T188A, T217A, S64A) [38]–[40] or control vector were co-transfected (0.6–1.0 µg total DNA). Luciferase activity was determined and normalized to that of β-galactosidase [38] using the Luciferase Assay System and β-Galactosidase Enzyme Assay System Kits, respectively (Promega). Each experiment was repeated at least three times, and triplicate samples were employed for each sample. Expression of the C/EBP-β phospho-acceptor mutant proteins was checked for equal expression by western blot.\n"}
testone
{"project":"testone","denotations":[{"id":"T7177","span":{"begin":959,"end":969},"obj":"Gene_expression"},{"id":"T7176","span":{"begin":878,"end":888},"obj":"Gene_expression"},{"id":"T7175","span":{"begin":896,"end":927},"obj":"Protein"},{"id":"T7174","span":{"begin":707,"end":722},"obj":"Protein"},{"id":"T7173","span":{"begin":679,"end":689},"obj":"Protein"},{"id":"T7172","span":{"begin":648,"end":663},"obj":"Protein"},{"id":"T7171","span":{"begin":587,"end":597},"obj":"Protein"},{"id":"T7170","span":{"begin":509,"end":513},"obj":"Protein"},{"id":"T7169","span":{"begin":502,"end":507},"obj":"Protein"},{"id":"T7168","span":{"begin":495,"end":500},"obj":"Protein"},{"id":"T7167","span":{"begin":461,"end":493},"obj":"Protein"},{"id":"T7166","span":{"begin":450,"end":457},"obj":"Protein"},{"id":"T7165","span":{"begin":122,"end":137},"obj":"Protein"},{"id":"T7164","span":{"begin":114,"end":121},"obj":"Protein"},{"id":"T7163","span":{"begin":64,"end":74},"obj":"Protein"},{"id":"T7162","span":{"begin":0,"end":5},"obj":"Protein"}],"relations":[{"id":"R5184","pred":"equivalentTo","subj":"T7168","obj":"T7167"},{"id":"R5185","pred":"themeOf","subj":"T7175","obj":"T7177"},{"id":"R5186","pred":"themeOf","subj":"T7175","obj":"T7176"}],"text":"Cebpb −/− MEFs (1×105) [34] were transfected with the indicated luciferase reporter plasmid (400 ng) along with a β-actin-β-galactosidase reporter plasmid (200 ng) by electroporation using the Invitrogen Neon™ system (1 pulse, 1350 V, 30 msec). Transfected cells were transferred to pre-warmed media in 24 well plates and incubated for 48 hrs prior to incubation with LPS (100 ng/ml) for 4 hrs where indicated. In some experiments, plasmids encoding C/EBP-β or C/EBP-β phospho-acceptor mutants (T188A, T217A, S64A) [38]–[40] or control vector were co-transfected (0.6–1.0 µg total DNA). Luciferase activity was determined and normalized to that of β-galactosidase [38] using the Luciferase Assay System and β-Galactosidase Enzyme Assay System Kits, respectively (Promega). Each experiment was repeated at least three times, and triplicate samples were employed for each sample. Expression of the C/EBP-β phospho-acceptor mutant proteins was checked for equal expression by western blot.\n"}
test3
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