tf-1 gas flow metre Search Results


90
YUTAKA Engineering Corporation tf-1 gas flow meter
Tf 1 Gas Flow Meter, supplied by YUTAKA Engineering Corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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tf-1  (ATCC)
97
ATCC tf-1
Tf 1, supplied by ATCC, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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94
DSMZ tf1 cells
Fig. 3. Effect of TNFa on GATA-1 transcriptional activity (A) <t>TF1</t> cells were co- transfected with the GATA-1-expressing vector, pXM-GATA1 and the reporter luciferase plasmids, pGL3-GATA-Luc and pHRG-TK. Transfected cells were treated for 2 h with TNFa or left untreated prior to analysis of luciferase activity. Firefly activity was normalized to Renilla, and the results are expressed as a ratio in arbitrary units. The data are presented as mean S.D. of three independent experiments (**P 0.01 and ***P < 0.001). (B) GATA-1 protein expression in TF1 cells cultured in the presence of GM-CSF (GM) or GM-CSF and TNFa (GM/TNF) was assessed by western blot analysis. Nuclear extracts from human erythroleukemia HEL cells were used as a positive control. b actin was used as an internal control.
Tf1 Cells, supplied by DSMZ, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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CLS Cell Lines Service GmbH tf-1 cells
Fig. 3. Effect of TNFa on GATA-1 transcriptional activity (A) <t>TF1</t> cells were co- transfected with the GATA-1-expressing vector, pXM-GATA1 and the reporter luciferase plasmids, pGL3-GATA-Luc and pHRG-TK. Transfected cells were treated for 2 h with TNFa or left untreated prior to analysis of luciferase activity. Firefly activity was normalized to Renilla, and the results are expressed as a ratio in arbitrary units. The data are presented as mean S.D. of three independent experiments (**P 0.01 and ***P < 0.001). (B) GATA-1 protein expression in TF1 cells cultured in the presence of GM-CSF (GM) or GM-CSF and TNFa (GM/TNF) was assessed by western blot analysis. Nuclear extracts from human erythroleukemia HEL cells were used as a positive control. b actin was used as an internal control.
Tf 1 Cells, supplied by CLS Cell Lines Service GmbH, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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ImmunoTools tf-1 cell
Fig. 3. Effect of TNFa on GATA-1 transcriptional activity (A) <t>TF1</t> cells were co- transfected with the GATA-1-expressing vector, pXM-GATA1 and the reporter luciferase plasmids, pGL3-GATA-Luc and pHRG-TK. Transfected cells were treated for 2 h with TNFa or left untreated prior to analysis of luciferase activity. Firefly activity was normalized to Renilla, and the results are expressed as a ratio in arbitrary units. The data are presented as mean S.D. of three independent experiments (**P 0.01 and ***P < 0.001). (B) GATA-1 protein expression in TF1 cells cultured in the presence of GM-CSF (GM) or GM-CSF and TNFa (GM/TNF) was assessed by western blot analysis. Nuclear extracts from human erythroleukemia HEL cells were used as a positive control. b actin was used as an internal control.
Tf 1 Cell, supplied by ImmunoTools, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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90
StemCells Inc tf-1 cells
Fig. 3. Effect of TNFa on GATA-1 transcriptional activity (A) <t>TF1</t> cells were co- transfected with the GATA-1-expressing vector, pXM-GATA1 and the reporter luciferase plasmids, pGL3-GATA-Luc and pHRG-TK. Transfected cells were treated for 2 h with TNFa or left untreated prior to analysis of luciferase activity. Firefly activity was normalized to Renilla, and the results are expressed as a ratio in arbitrary units. The data are presented as mean S.D. of three independent experiments (**P 0.01 and ***P < 0.001). (B) GATA-1 protein expression in TF1 cells cultured in the presence of GM-CSF (GM) or GM-CSF and TNFa (GM/TNF) was assessed by western blot analysis. Nuclear extracts from human erythroleukemia HEL cells were used as a positive control. b actin was used as an internal control.
Tf 1 Cells, supplied by StemCells Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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90
AbCys s a tf-1 cells
Fig. 3. Effect of TNFa on GATA-1 transcriptional activity (A) <t>TF1</t> cells were co- transfected with the GATA-1-expressing vector, pXM-GATA1 and the reporter luciferase plasmids, pGL3-GATA-Luc and pHRG-TK. Transfected cells were treated for 2 h with TNFa or left untreated prior to analysis of luciferase activity. Firefly activity was normalized to Renilla, and the results are expressed as a ratio in arbitrary units. The data are presented as mean S.D. of three independent experiments (**P 0.01 and ***P < 0.001). (B) GATA-1 protein expression in TF1 cells cultured in the presence of GM-CSF (GM) or GM-CSF and TNFa (GM/TNF) was assessed by western blot analysis. Nuclear extracts from human erythroleukemia HEL cells were used as a positive control. b actin was used as an internal control.
Tf 1 Cells, supplied by AbCys s a, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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90
STEMCELL Technologies Inc methocult h4230
Fig. 3. Effect of TNFa on GATA-1 transcriptional activity (A) <t>TF1</t> cells were co- transfected with the GATA-1-expressing vector, pXM-GATA1 and the reporter luciferase plasmids, pGL3-GATA-Luc and pHRG-TK. Transfected cells were treated for 2 h with TNFa or left untreated prior to analysis of luciferase activity. Firefly activity was normalized to Renilla, and the results are expressed as a ratio in arbitrary units. The data are presented as mean S.D. of three independent experiments (**P 0.01 and ***P < 0.001). (B) GATA-1 protein expression in TF1 cells cultured in the presence of GM-CSF (GM) or GM-CSF and TNFa (GM/TNF) was assessed by western blot analysis. Nuclear extracts from human erythroleukemia HEL cells were used as a positive control. b actin was used as an internal control.
Methocult H4230, supplied by STEMCELL Technologies Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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90
BioResource International Inc tf-1 cells
Fig. 3. Effect of TNFa on GATA-1 transcriptional activity (A) <t>TF1</t> cells were co- transfected with the GATA-1-expressing vector, pXM-GATA1 and the reporter luciferase plasmids, pGL3-GATA-Luc and pHRG-TK. Transfected cells were treated for 2 h with TNFa or left untreated prior to analysis of luciferase activity. Firefly activity was normalized to Renilla, and the results are expressed as a ratio in arbitrary units. The data are presented as mean S.D. of three independent experiments (**P 0.01 and ***P < 0.001). (B) GATA-1 protein expression in TF1 cells cultured in the presence of GM-CSF (GM) or GM-CSF and TNFa (GM/TNF) was assessed by western blot analysis. Nuclear extracts from human erythroleukemia HEL cells were used as a positive control. b actin was used as an internal control.
Tf 1 Cells, supplied by BioResource International Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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90
Promega mts/pms cell proliferation assay
Fig. 3. Effect of TNFa on GATA-1 transcriptional activity (A) <t>TF1</t> cells were co- transfected with the GATA-1-expressing vector, pXM-GATA1 and the reporter luciferase plasmids, pGL3-GATA-Luc and pHRG-TK. Transfected cells were treated for 2 h with TNFa or left untreated prior to analysis of luciferase activity. Firefly activity was normalized to Renilla, and the results are expressed as a ratio in arbitrary units. The data are presented as mean S.D. of three independent experiments (**P 0.01 and ***P < 0.001). (B) GATA-1 protein expression in TF1 cells cultured in the presence of GM-CSF (GM) or GM-CSF and TNFa (GM/TNF) was assessed by western blot analysis. Nuclear extracts from human erythroleukemia HEL cells were used as a positive control. b actin was used as an internal control.
Mts/Pms Cell Proliferation Assay, supplied by Promega, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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86
Novo Nordisk lipidated tf 1 244
Fig. 3. Effect of TNFa on GATA-1 transcriptional activity (A) <t>TF1</t> cells were co- transfected with the GATA-1-expressing vector, pXM-GATA1 and the reporter luciferase plasmids, pGL3-GATA-Luc and pHRG-TK. Transfected cells were treated for 2 h with TNFa or left untreated prior to analysis of luciferase activity. Firefly activity was normalized to Renilla, and the results are expressed as a ratio in arbitrary units. The data are presented as mean S.D. of three independent experiments (**P 0.01 and ***P < 0.001). (B) GATA-1 protein expression in TF1 cells cultured in the presence of GM-CSF (GM) or GM-CSF and TNFa (GM/TNF) was assessed by western blot analysis. Nuclear extracts from human erythroleukemia HEL cells were used as a positive control. b actin was used as an internal control.
Lipidated Tf 1 244, supplied by Novo Nordisk, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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90
BioResource International Inc tf-1 cell line bcrc number 60323
Fig. 3. Effect of TNFa on GATA-1 transcriptional activity (A) <t>TF1</t> cells were co- transfected with the GATA-1-expressing vector, pXM-GATA1 and the reporter luciferase plasmids, pGL3-GATA-Luc and pHRG-TK. Transfected cells were treated for 2 h with TNFa or left untreated prior to analysis of luciferase activity. Firefly activity was normalized to Renilla, and the results are expressed as a ratio in arbitrary units. The data are presented as mean S.D. of three independent experiments (**P 0.01 and ***P < 0.001). (B) GATA-1 protein expression in TF1 cells cultured in the presence of GM-CSF (GM) or GM-CSF and TNFa (GM/TNF) was assessed by western blot analysis. Nuclear extracts from human erythroleukemia HEL cells were used as a positive control. b actin was used as an internal control.
Tf 1 Cell Line Bcrc Number 60323, supplied by BioResource International Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Fig. 3. Effect of TNFa on GATA-1 transcriptional activity (A) TF1 cells were co- transfected with the GATA-1-expressing vector, pXM-GATA1 and the reporter luciferase plasmids, pGL3-GATA-Luc and pHRG-TK. Transfected cells were treated for 2 h with TNFa or left untreated prior to analysis of luciferase activity. Firefly activity was normalized to Renilla, and the results are expressed as a ratio in arbitrary units. The data are presented as mean S.D. of three independent experiments (**P 0.01 and ***P < 0.001). (B) GATA-1 protein expression in TF1 cells cultured in the presence of GM-CSF (GM) or GM-CSF and TNFa (GM/TNF) was assessed by western blot analysis. Nuclear extracts from human erythroleukemia HEL cells were used as a positive control. b actin was used as an internal control.

Journal: Biochemical pharmacology

Article Title: Tumor necrosis factor α-mediated inhibition of erythropoiesis involves GATA-1/GATA-2 balance impairment and PU.1 over-expression.

doi: 10.1016/j.bcp.2011.03.030

Figure Lengend Snippet: Fig. 3. Effect of TNFa on GATA-1 transcriptional activity (A) TF1 cells were co- transfected with the GATA-1-expressing vector, pXM-GATA1 and the reporter luciferase plasmids, pGL3-GATA-Luc and pHRG-TK. Transfected cells were treated for 2 h with TNFa or left untreated prior to analysis of luciferase activity. Firefly activity was normalized to Renilla, and the results are expressed as a ratio in arbitrary units. The data are presented as mean S.D. of three independent experiments (**P 0.01 and ***P < 0.001). (B) GATA-1 protein expression in TF1 cells cultured in the presence of GM-CSF (GM) or GM-CSF and TNFa (GM/TNF) was assessed by western blot analysis. Nuclear extracts from human erythroleukemia HEL cells were used as a positive control. b actin was used as an internal control.

Article Snippet: TF1 cells were provided by DSMZ (Deutsche Sammlung für Mikroorganismen und Zellkulturen; Braunschweig, Germany).

Techniques: Activity Assay, Transfection, Expressing, Plasmid Preparation, Luciferase, Cell Culture, Western Blot, Positive Control, Control