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quantitative pcr results  (GraphPad Software Inc)
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GraphPad Software Inc quantitative pcr results
Quantitative Pcr Results, supplied by GraphPad Software 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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quantitative rt-pcr results  (Illumina Inc)
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Illumina Inc quantitative rt-pcr results
Quantitative Rt Pcr Results, supplied by Illumina 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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quantitative reverse transcription pcr results  (GraphPad Software Inc)
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GraphPad Software Inc quantitative reverse transcription pcr results
Correlation of ERRβ expression with ERα in breast tumors and cell lines. a Immunohistochemical staining with ERRβ antibody in ER + ve and ER-ve breast cancer patients. Elevated expression of ERRβ was found in ER + ve ( n = 6) compared to ER-ve ( n = 6) breast cancer patient samples. b Graphical representation of IHC composite scores of each tissue microarray sample showing significant elevated expression of ERRβ in ER + ve than in ER-ve breast cancer patient samples. Graph was plotted using composite score and p -values were calculated using 2-group t-test ( p < 0.05 considered as significant). c , d Western blots, Reverse <t>transcription</t> polymerase chain reaction (RT <t>PCR)</t> and densitometry analysis results representing elevated levels of ERRβ in ER + ve breast cancer cells (* p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001). Statistical significance for relative gene expression (RT PCR) and normalized percentage of expression (WB) was analyzed using One-way ANOVA and unpaired t-test respectively ( p -value < 0.05 was considered as significant)
Quantitative Reverse Transcription Pcr Results, supplied by GraphPad Software 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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real time quantitative rt-pcr results  (National Research Council Canada)
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National Research Council Canada real time quantitative rt-pcr results
Correlation of ERRβ expression with ERα in breast tumors and cell lines. a Immunohistochemical staining with ERRβ antibody in ER + ve and ER-ve breast cancer patients. Elevated expression of ERRβ was found in ER + ve ( n = 6) compared to ER-ve ( n = 6) breast cancer patient samples. b Graphical representation of IHC composite scores of each tissue microarray sample showing significant elevated expression of ERRβ in ER + ve than in ER-ve breast cancer patient samples. Graph was plotted using composite score and p -values were calculated using 2-group t-test ( p < 0.05 considered as significant). c , d Western blots, Reverse <t>transcription</t> polymerase chain reaction (RT <t>PCR)</t> and densitometry analysis results representing elevated levels of ERRβ in ER + ve breast cancer cells (* p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001). Statistical significance for relative gene expression (RT PCR) and normalized percentage of expression (WB) was analyzed using One-way ANOVA and unpaired t-test respectively ( p -value < 0.05 was considered as significant)
Real Time Quantitative Rt Pcr Results, supplied by National Research Council Canada, 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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quantitative pcr results  (SAS institute)
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SAS institute quantitative pcr results
Correlation of ERRβ expression with ERα in breast tumors and cell lines. a Immunohistochemical staining with ERRβ antibody in ER + ve and ER-ve breast cancer patients. Elevated expression of ERRβ was found in ER + ve ( n = 6) compared to ER-ve ( n = 6) breast cancer patient samples. b Graphical representation of IHC composite scores of each tissue microarray sample showing significant elevated expression of ERRβ in ER + ve than in ER-ve breast cancer patient samples. Graph was plotted using composite score and p -values were calculated using 2-group t-test ( p < 0.05 considered as significant). c , d Western blots, Reverse <t>transcription</t> polymerase chain reaction (RT <t>PCR)</t> and densitometry analysis results representing elevated levels of ERRβ in ER + ve breast cancer cells (* p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001). Statistical significance for relative gene expression (RT PCR) and normalized percentage of expression (WB) was analyzed using One-way ANOVA and unpaired t-test respectively ( p -value < 0.05 was considered as significant)
Quantitative Pcr Results, supplied by SAS institute, 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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Correlation of ERRβ expression with ERα in breast tumors and cell lines. a Immunohistochemical staining with ERRβ antibody in ER + ve and ER-ve breast cancer patients. Elevated expression of ERRβ was found in ER + ve ( n = 6) compared to ER-ve ( n = 6) breast cancer patient samples. b Graphical representation of IHC composite scores of each tissue microarray sample showing significant elevated expression of ERRβ in ER + ve than in ER-ve breast cancer patient samples. Graph was plotted using composite score and p -values were calculated using 2-group t-test ( p < 0.05 considered as significant). c , d Western blots, Reverse transcription polymerase chain reaction (RT PCR) and densitometry analysis results representing elevated levels of ERRβ in ER + ve breast cancer cells (* p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001). Statistical significance for relative gene expression (RT PCR) and normalized percentage of expression (WB) was analyzed using One-way ANOVA and unpaired t-test respectively ( p -value < 0.05 was considered as significant)

Journal: BMC Cancer

Article Title: Estrogen receptor α dependent regulation of estrogen related receptor β and its role in cell cycle in breast cancer

doi: 10.1186/s12885-018-4528-x

Figure Lengend Snippet: Correlation of ERRβ expression with ERα in breast tumors and cell lines. a Immunohistochemical staining with ERRβ antibody in ER + ve and ER-ve breast cancer patients. Elevated expression of ERRβ was found in ER + ve ( n = 6) compared to ER-ve ( n = 6) breast cancer patient samples. b Graphical representation of IHC composite scores of each tissue microarray sample showing significant elevated expression of ERRβ in ER + ve than in ER-ve breast cancer patient samples. Graph was plotted using composite score and p -values were calculated using 2-group t-test ( p < 0.05 considered as significant). c , d Western blots, Reverse transcription polymerase chain reaction (RT PCR) and densitometry analysis results representing elevated levels of ERRβ in ER + ve breast cancer cells (* p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001). Statistical significance for relative gene expression (RT PCR) and normalized percentage of expression (WB) was analyzed using One-way ANOVA and unpaired t-test respectively ( p -value < 0.05 was considered as significant)

Article Snippet: The Quantitative reverse transcription PCR results were plotted using GraphPad Prism version 6.01.

Techniques: Expressing, Immunohistochemical staining, Staining, Microarray, Western Blot, Reverse Transcription, Polymerase Chain Reaction, Reverse Transcription Polymerase Chain Reaction, Gene Expression

Expression of ERRβ is ERα dependent. Efficient knockdown of ERα showing significant decrease in the expression of ERRβ in MCF7 cells. a , b Quantitative Real-time PCR (qRT-PCR) and Reverse transcription polymerase chain reaction (RT-PCR) results showing decreased expression of ERRβ in ERα depleted MCF7 cells. Housekeeping gene GAPDH treated as control and ΔCt, ΔΔCt, 2 -ΔΔCt values were calculated and graph was plotted using 2 -ΔΔCt values. Fold change ≥ 2 was considered as significant. p -values were calculated using 2-group t-test (* p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001). c Western blot revealing the depleted expression of ERRβ in ERα Knockdown MCF7 (ERα KD) cells

Journal: BMC Cancer

Article Title: Estrogen receptor α dependent regulation of estrogen related receptor β and its role in cell cycle in breast cancer

doi: 10.1186/s12885-018-4528-x

Figure Lengend Snippet: Expression of ERRβ is ERα dependent. Efficient knockdown of ERα showing significant decrease in the expression of ERRβ in MCF7 cells. a , b Quantitative Real-time PCR (qRT-PCR) and Reverse transcription polymerase chain reaction (RT-PCR) results showing decreased expression of ERRβ in ERα depleted MCF7 cells. Housekeeping gene GAPDH treated as control and ΔCt, ΔΔCt, 2 -ΔΔCt values were calculated and graph was plotted using 2 -ΔΔCt values. Fold change ≥ 2 was considered as significant. p -values were calculated using 2-group t-test (* p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001). c Western blot revealing the depleted expression of ERRβ in ERα Knockdown MCF7 (ERα KD) cells

Article Snippet: The Quantitative reverse transcription PCR results were plotted using GraphPad Prism version 6.01.

Techniques: Expressing, Knockdown, Real-time Polymerase Chain Reaction, Quantitative RT-PCR, Reverse Transcription, Polymerase Chain Reaction, Reverse Transcription Polymerase Chain Reaction, Control, Western Blot