goat anti-rabbit igg Search Results


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  • 99
    Vector Laboratories biotinylated goat anti rabbit igg
    Biotinylated Goat Anti Rabbit Igg, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 99/100, based on 10708 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    LI-COR irdye 800cw goat anti rabbit igg h l
    Irdye 800cw Goat Anti Rabbit Igg H L, supplied by LI-COR, used in various techniques. Bioz Stars score: 99/100, based on 3552 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Thermo Fisher goat anti rabbit igg h l cross adsorbed secondary antibody
    Goat Anti Rabbit Igg H L Cross Adsorbed Secondary Antibody, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 14192 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Thermo Fisher goat anti rabbit igg h l highly cross adsorbed secondary antibody
    Goat Anti Rabbit Igg H L Highly Cross Adsorbed Secondary Antibody, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 11273 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Abcam goat anti rabbit igg h l hrp
    Goat Anti Rabbit Igg H L Hrp, supplied by Abcam, used in various techniques. Bioz Stars score: 99/100, based on 2991 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Millipore anti rabbit igg whole molecule peroxidase antibody
    Anti Rabbit Igg Whole Molecule Peroxidase Antibody, supplied by Millipore, used in various techniques. Bioz Stars score: 99/100, based on 7032 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Santa Cruz Biotechnology goat anti rabbit igg hrp
    Goat Anti Rabbit Igg Hrp, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 99/100, based on 5529 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Jackson Immuno peroxidase affinipure goat anti rabbit igg
    Peroxidase Affinipure Goat Anti Rabbit Igg, supplied by Jackson Immuno, used in various techniques. Bioz Stars score: 99/100, based on 4084 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Thermo Fisher alexa fluor 488 conjugated goat anti rabbit igg
    Alexa Fluor 488 Conjugated Goat Anti Rabbit Igg, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 5235 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Santa Cruz Biotechnology goat anti rabbit igg
    CHKA2 co-immunoprecipitates with exogenous or endogenous full length EGFR A. Plasmids encoding full length EGFR and flag-tagged CHKA2 (f-CHKA2) were cotransfected into 293T cells along those encoding K + or K − <t>c-Src</t> and analyzed as in Figure 1A , except that mab108 was used instead of myc Ab for immunoprecipitation of EGFR. B–D. Indicated cells were serum starved overnight and stimulated with 50 ( B ), 10 ( C ) or 5 ng/mL ( D ) EGF for the indicated times. CHKA was immunoprecipitated with rabbit anti-CHKA antibody and rabbit <t>IgG</t> was used as a negative control (crtl IgG). Immunoblotting was carried out as described in Materials and Methods.
    Goat Anti Rabbit Igg, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 92/100, based on 3649 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Thermo Fisher goat anti rabbit igg h l secondary antibody
    CHKA2 co-immunoprecipitates with exogenous or endogenous full length EGFR A. Plasmids encoding full length EGFR and flag-tagged CHKA2 (f-CHKA2) were cotransfected into 293T cells along those encoding K + or K − <t>c-Src</t> and analyzed as in Figure 1A , except that mab108 was used instead of myc Ab for immunoprecipitation of EGFR. B–D. Indicated cells were serum starved overnight and stimulated with 50 ( B ), 10 ( C ) or 5 ng/mL ( D ) EGF for the indicated times. CHKA was immunoprecipitated with rabbit anti-CHKA antibody and rabbit <t>IgG</t> was used as a negative control (crtl IgG). Immunoblotting was carried out as described in Materials and Methods.
    Goat Anti Rabbit Igg H L Secondary Antibody, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 1787 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Thermo Fisher alexa fluor 594 goat anti rabbit igg
    CHKA2 co-immunoprecipitates with exogenous or endogenous full length EGFR A. Plasmids encoding full length EGFR and flag-tagged CHKA2 (f-CHKA2) were cotransfected into 293T cells along those encoding K + or K − <t>c-Src</t> and analyzed as in Figure 1A , except that mab108 was used instead of myc Ab for immunoprecipitation of EGFR. B–D. Indicated cells were serum starved overnight and stimulated with 50 ( B ), 10 ( C ) or 5 ng/mL ( D ) EGF for the indicated times. CHKA was immunoprecipitated with rabbit anti-CHKA antibody and rabbit <t>IgG</t> was used as a negative control (crtl IgG). Immunoblotting was carried out as described in Materials and Methods.
    Alexa Fluor 594 Goat Anti Rabbit Igg, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 2663 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Vector Laboratories biotinylated goat anti rabbit igg antibody
    CHKA2 co-immunoprecipitates with exogenous or endogenous full length EGFR A. Plasmids encoding full length EGFR and flag-tagged CHKA2 (f-CHKA2) were cotransfected into 293T cells along those encoding K + or K − <t>c-Src</t> and analyzed as in Figure 1A , except that mab108 was used instead of myc Ab for immunoprecipitation of EGFR. B–D. Indicated cells were serum starved overnight and stimulated with 50 ( B ), 10 ( C ) or 5 ng/mL ( D ) EGF for the indicated times. CHKA was immunoprecipitated with rabbit anti-CHKA antibody and rabbit <t>IgG</t> was used as a negative control (crtl IgG). Immunoblotting was carried out as described in Materials and Methods.
    Biotinylated Goat Anti Rabbit Igg Antibody, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 99/100, based on 1489 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Bio-Rad goat anti rabbit
    CHKA2 co-immunoprecipitates with exogenous or endogenous full length EGFR A. Plasmids encoding full length EGFR and flag-tagged CHKA2 (f-CHKA2) were cotransfected into 293T cells along those encoding K + or K − <t>c-Src</t> and analyzed as in Figure 1A , except that mab108 was used instead of myc Ab for immunoprecipitation of EGFR. B–D. Indicated cells were serum starved overnight and stimulated with 50 ( B ), 10 ( C ) or 5 ng/mL ( D ) EGF for the indicated times. CHKA was immunoprecipitated with rabbit anti-CHKA antibody and rabbit <t>IgG</t> was used as a negative control (crtl IgG). Immunoblotting was carried out as described in Materials and Methods.
    Goat Anti Rabbit, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 99/100, based on 1737 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Bio-Rad goat anti rabbit igg
    CHKA2 co-immunoprecipitates with exogenous or endogenous full length EGFR A. Plasmids encoding full length EGFR and flag-tagged CHKA2 (f-CHKA2) were cotransfected into 293T cells along those encoding K + or K − <t>c-Src</t> and analyzed as in Figure 1A , except that mab108 was used instead of myc Ab for immunoprecipitation of EGFR. B–D. Indicated cells were serum starved overnight and stimulated with 50 ( B ), 10 ( C ) or 5 ng/mL ( D ) EGF for the indicated times. CHKA was immunoprecipitated with rabbit anti-CHKA antibody and rabbit <t>IgG</t> was used as a negative control (crtl IgG). Immunoblotting was carried out as described in Materials and Methods.
    Goat Anti Rabbit Igg, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 99/100, based on 1516 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Abcam goat anti rabbit igg
    CHKA2 co-immunoprecipitates with exogenous or endogenous full length EGFR A. Plasmids encoding full length EGFR and flag-tagged CHKA2 (f-CHKA2) were cotransfected into 293T cells along those encoding K + or K − <t>c-Src</t> and analyzed as in Figure 1A , except that mab108 was used instead of myc Ab for immunoprecipitation of EGFR. B–D. Indicated cells were serum starved overnight and stimulated with 50 ( B ), 10 ( C ) or 5 ng/mL ( D ) EGF for the indicated times. CHKA was immunoprecipitated with rabbit anti-CHKA antibody and rabbit <t>IgG</t> was used as a negative control (crtl IgG). Immunoblotting was carried out as described in Materials and Methods.
    Goat Anti Rabbit Igg, supplied by Abcam, used in various techniques. Bioz Stars score: 99/100, based on 1810 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Thermo Fisher f ab 2 goat anti rabbit igg h l cross adsorbed secondary antibody
    CHKA2 co-immunoprecipitates with exogenous or endogenous full length EGFR A. Plasmids encoding full length EGFR and flag-tagged CHKA2 (f-CHKA2) were cotransfected into 293T cells along those encoding K + or K − <t>c-Src</t> and analyzed as in Figure 1A , except that mab108 was used instead of myc Ab for immunoprecipitation of EGFR. B–D. Indicated cells were serum starved overnight and stimulated with 50 ( B ), 10 ( C ) or 5 ng/mL ( D ) EGF for the indicated times. CHKA was immunoprecipitated with rabbit anti-CHKA antibody and rabbit <t>IgG</t> was used as a negative control (crtl IgG). Immunoblotting was carried out as described in Materials and Methods.
    F Ab 2 Goat Anti Rabbit Igg H L Cross Adsorbed Secondary Antibody, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 1504 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Image Search Results


    CHKA2 co-immunoprecipitates with exogenous or endogenous full length EGFR A. Plasmids encoding full length EGFR and flag-tagged CHKA2 (f-CHKA2) were cotransfected into 293T cells along those encoding K + or K − c-Src and analyzed as in Figure 1A , except that mab108 was used instead of myc Ab for immunoprecipitation of EGFR. B–D. Indicated cells were serum starved overnight and stimulated with 50 ( B ), 10 ( C ) or 5 ng/mL ( D ) EGF for the indicated times. CHKA was immunoprecipitated with rabbit anti-CHKA antibody and rabbit IgG was used as a negative control (crtl IgG). Immunoblotting was carried out as described in Materials and Methods.

    Journal: Oncogene

    Article Title: Functional interactions between Choline kinase ?, epidermal growth factor receptor (EGFR), and c-Src in breast cancer cell proliferations

    doi: 10.1038/onc.2011.332

    Figure Lengend Snippet: CHKA2 co-immunoprecipitates with exogenous or endogenous full length EGFR A. Plasmids encoding full length EGFR and flag-tagged CHKA2 (f-CHKA2) were cotransfected into 293T cells along those encoding K + or K − c-Src and analyzed as in Figure 1A , except that mab108 was used instead of myc Ab for immunoprecipitation of EGFR. B–D. Indicated cells were serum starved overnight and stimulated with 50 ( B ), 10 ( C ) or 5 ng/mL ( D ) EGF for the indicated times. CHKA was immunoprecipitated with rabbit anti-CHKA antibody and rabbit IgG was used as a negative control (crtl IgG). Immunoblotting was carried out as described in Materials and Methods.

    Article Snippet: Immunoblotting was performed using standard methods with the following antibodies: rabbit anti-myc-tag, EGFR, and c-Src (Cell Signaling), rabbit anti-flag-tag (Sigma-Aldrich), GAPDH (Millipore), and HRP-conjugated pY99, goat anti-rabbit IgG (Santa Cruz Biotechnology, Santa Cruz, CA), sheep anti-mouse IgG (GE Healthcare, Piscataway, NJ) and native IgG detection reagent (HRP) (Thermo Fisher Scientific).

    Techniques: Immunoprecipitation, Negative Control

    CHKA2 co-immunoprecipitates with EGFR kinase domain in a c-Src activity dependent manner in 293T cells A. Plasmids encoding flag-tagged CHKA2 and myc-tagged EGFR kinase domain (EGFR-K, aa 672–960) were co-transfected with those encoding wt (K+) or kinase-defective (K−) c-Src into 293T cells. Where indicated, the amount of total DNA for transfection was adjusted with the corresponding empty vectors (−). Lysates were examined for levels of specific proteins or used for co-immunoprecipitation as described in Materials and Methods. Western blotting of whole cell lysates (Lysate) is shown in the left panel and of CHKA2 and EGFR immunoprecipitates in the middle and right panels, respectively. The same amount of mouse IgG was used for negative control (CTRL) immunoprecipitation as for CHKA2 (lane 10–12). Immunprecipitated proteins were detected by Western blotting with the indicated antibodies. B. Plasmids encoding flag-tagged CHKA2 and various myc-tagged domains of the cytosolic region of EGFR (diagram, left) were co-transfected into 293T cells with those encoding wild type (K+) or kinase-defective (K−) c-Src and analyzed as in Panel A. Constructs containing the kinase domain of EGFR associated with CHKA2 in a c-Src-activity dependent manner.

    Journal: Oncogene

    Article Title: Functional interactions between Choline kinase ?, epidermal growth factor receptor (EGFR), and c-Src in breast cancer cell proliferations

    doi: 10.1038/onc.2011.332

    Figure Lengend Snippet: CHKA2 co-immunoprecipitates with EGFR kinase domain in a c-Src activity dependent manner in 293T cells A. Plasmids encoding flag-tagged CHKA2 and myc-tagged EGFR kinase domain (EGFR-K, aa 672–960) were co-transfected with those encoding wt (K+) or kinase-defective (K−) c-Src into 293T cells. Where indicated, the amount of total DNA for transfection was adjusted with the corresponding empty vectors (−). Lysates were examined for levels of specific proteins or used for co-immunoprecipitation as described in Materials and Methods. Western blotting of whole cell lysates (Lysate) is shown in the left panel and of CHKA2 and EGFR immunoprecipitates in the middle and right panels, respectively. The same amount of mouse IgG was used for negative control (CTRL) immunoprecipitation as for CHKA2 (lane 10–12). Immunprecipitated proteins were detected by Western blotting with the indicated antibodies. B. Plasmids encoding flag-tagged CHKA2 and various myc-tagged domains of the cytosolic region of EGFR (diagram, left) were co-transfected into 293T cells with those encoding wild type (K+) or kinase-defective (K−) c-Src and analyzed as in Panel A. Constructs containing the kinase domain of EGFR associated with CHKA2 in a c-Src-activity dependent manner.

    Article Snippet: Immunoblotting was performed using standard methods with the following antibodies: rabbit anti-myc-tag, EGFR, and c-Src (Cell Signaling), rabbit anti-flag-tag (Sigma-Aldrich), GAPDH (Millipore), and HRP-conjugated pY99, goat anti-rabbit IgG (Santa Cruz Biotechnology, Santa Cruz, CA), sheep anti-mouse IgG (GE Healthcare, Piscataway, NJ) and native IgG detection reagent (HRP) (Thermo Fisher Scientific).

    Techniques: Activity Assay, Transfection, Immunoprecipitation, Western Blot, Negative Control, Construct