p src y416  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc p src y416
    P Src Y416, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    rabbit anti phospho src family y416  (Cell Signaling Technology Inc)


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    phospho src y416  (Cell Signaling Technology Inc)


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    p src y416  (Cell Signaling Technology Inc)


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    anti phospho c src y416  (Cell Signaling Technology Inc)


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    p src y416  (Cell Signaling Technology Inc)


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    p src y416  (Cell Signaling Technology Inc)


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    rabbit anti phospho src y416  (Cell Signaling Technology Inc)


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    antibodies against phospho src y416  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc antibodies against phospho src y416
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    antibodies against phospho src y416  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc antibodies against phospho src y416
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    phospho src y416  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc phospho src y416
    A-B , representative immunoblots showing the expression of Gα i2 R179C and Gα oA R243H in MCF10A cells ( A ) and activation of <t>c-Src</t> and STAT3 by phosphorylation of Src <t>Y416</t> and STAT3 Y705 in MCF10A cells treated with vehicle control (CT), 2 μM of saracatinib (sara) and STAT3-IN-1 (STAT3i) (B) . CD , the effect of Gα i2 R179C and Gα oA R243H expression on the growth of MCF10A cells in 2D culture ( C ) and in Matrigel ( D ). E , representative images showing the absence of tumor formation in nude mice orthotopically implanted with MCF10A cells expressing GFP, Gα i2 R179C or Gα oA R243H. *, **,*** p<0.05, 0.01 and 0.001 vs. GFP, n=4-6. One-way ANOVA was used for statistical analysis in this Figure.
    Phospho Src Y416, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    1) Product Images from "Active Gαi/o mutants accelerate breast tumor metastasis via the c-Src pathway"

    Article Title: Active Gαi/o mutants accelerate breast tumor metastasis via the c-Src pathway

    Journal: bioRxiv

    doi: 10.1101/2023.01.16.524334

    A-B , representative immunoblots showing the expression of Gα i2 R179C and Gα oA R243H in MCF10A cells ( A ) and activation of c-Src and STAT3 by phosphorylation of Src Y416 and STAT3 Y705 in MCF10A cells treated with vehicle control (CT), 2 μM of saracatinib (sara) and STAT3-IN-1 (STAT3i) (B) . CD , the effect of Gα i2 R179C and Gα oA R243H expression on the growth of MCF10A cells in 2D culture ( C ) and in Matrigel ( D ). E , representative images showing the absence of tumor formation in nude mice orthotopically implanted with MCF10A cells expressing GFP, Gα i2 R179C or Gα oA R243H. *, **,*** p<0.05, 0.01 and 0.001 vs. GFP, n=4-6. One-way ANOVA was used for statistical analysis in this Figure.
    Figure Legend Snippet: A-B , representative immunoblots showing the expression of Gα i2 R179C and Gα oA R243H in MCF10A cells ( A ) and activation of c-Src and STAT3 by phosphorylation of Src Y416 and STAT3 Y705 in MCF10A cells treated with vehicle control (CT), 2 μM of saracatinib (sara) and STAT3-IN-1 (STAT3i) (B) . CD , the effect of Gα i2 R179C and Gα oA R243H expression on the growth of MCF10A cells in 2D culture ( C ) and in Matrigel ( D ). E , representative images showing the absence of tumor formation in nude mice orthotopically implanted with MCF10A cells expressing GFP, Gα i2 R179C or Gα oA R243H. *, **,*** p<0.05, 0.01 and 0.001 vs. GFP, n=4-6. One-way ANOVA was used for statistical analysis in this Figure.

    Techniques Used: Western Blot, Expressing, Activation Assay

    A-B , Western blotting ( A ) showing increased phosphorylation of c-Src Y416 and EGFR Y1068 and no change in phosphorylation of AKT s473 , STAT3 Y705 and HER2 Y1221/1222 in Neu/Gα i2 R179C tumors as compared to Neu tumors. Each lane represents a sample from an individual tumor. The Western blotting data from A were quantified and expressed as the ratio of the phosphorylated to total proteins ( B ). Two tail unpaired Student’s t test was used for statistical analysis of the data in B , and p values are shown. C-D , Western blotting showing phosphorylation of the indicated proteins in Neu cells expressing GFP, Gα i2 R179C (Gα i2 ) or Gα oA R243H (Gα oA ) and treated with vehicle control (CT) or saracatinib (sara; 2 μM) ( C ) and Neu cells overexpressing GFP or the constitutively active c-Src Y527F mutant ( D) . E , co-immunoprecipitation of ee-tagged Gα i2 R179C and Gα oA R243H with c-Src in Neu cells. Neu cells expressing GFP, Gα i2 R179C (Gα i2 ) or Gα oA R243H (Gα oA ) were immunoprecipitated with the anti-ee antibody and probed with the indicated antibodies.
    Figure Legend Snippet: A-B , Western blotting ( A ) showing increased phosphorylation of c-Src Y416 and EGFR Y1068 and no change in phosphorylation of AKT s473 , STAT3 Y705 and HER2 Y1221/1222 in Neu/Gα i2 R179C tumors as compared to Neu tumors. Each lane represents a sample from an individual tumor. The Western blotting data from A were quantified and expressed as the ratio of the phosphorylated to total proteins ( B ). Two tail unpaired Student’s t test was used for statistical analysis of the data in B , and p values are shown. C-D , Western blotting showing phosphorylation of the indicated proteins in Neu cells expressing GFP, Gα i2 R179C (Gα i2 ) or Gα oA R243H (Gα oA ) and treated with vehicle control (CT) or saracatinib (sara; 2 μM) ( C ) and Neu cells overexpressing GFP or the constitutively active c-Src Y527F mutant ( D) . E , co-immunoprecipitation of ee-tagged Gα i2 R179C and Gα oA R243H with c-Src in Neu cells. Neu cells expressing GFP, Gα i2 R179C (Gα i2 ) or Gα oA R243H (Gα oA ) were immunoprecipitated with the anti-ee antibody and probed with the indicated antibodies.

    Techniques Used: Western Blot, Expressing, Mutagenesis, Immunoprecipitation

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