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phospho er ser167  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc phospho er ser167
    Phospho Er Ser167, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 94/100, based on 21 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/anti+phospho+er+%CE%B1/Phospho-Estrogen+Receptor+alpha+(Ser167)+Rabbit+mAb/pm40796046-88-66-68
    Average 94 stars, based on 21 article reviews
    phospho er ser167 - by Bioz Stars, 2026-10
    94/100 stars

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    Related Articles

    Sequencing:

    Article Title: Anti-Inflammatory and Antimicrobial Effects of Estradiol in Bovine Mammary Epithelial Cells during Staphylococcus aureus Internalization
    Article Snippet: The monoclonal blocking antibodies anti- α 5 β 1 integrin (MAB2514) and anti-TLR2 (TLR2.1) were obtained from Millipore and Abcam, respectively.The monoclonal blocking antibodies anti- α 5 β 1 integrin (MAB2514) and anti-TLR2 (TLR2.1) were obtained from Millipore and Abcam, respectively.. The anti-phospho-ER α (2511S, Ser118) was obtained from Cell Signaling and the anti-ER β (517700) was acquired from Life Technologies.. The FITC-conjugated secondary antibodies against mouse and rat IgGs were purchased from Invitrogen and Thermo Scientific, respectively.The FITC-conjugated secondary antibodies against mouse and rat IgGs were purchased from Invitrogen and Thermo Scientific, respectively.

    Fluorescence:

    Article Title: Anti-Inflammatory and Antimicrobial Effects of Estradiol in Bovine Mammary Epithelial Cells during Staphylococcus aureus Internalization
    Article Snippet: The monoclonal blocking antibodies anti- α 5 β 1 integrin (MAB2514) and anti-TLR2 (TLR2.1) were obtained from Millipore and Abcam, respectively.The monoclonal blocking antibodies anti- α 5 β 1 integrin (MAB2514) and anti-TLR2 (TLR2.1) were obtained from Millipore and Abcam, respectively.. The anti-phospho-ER α (2511S, Ser118) was obtained from Cell Signaling and the anti-ER β (517700) was acquired from Life Technologies.. The FITC-conjugated secondary antibodies against mouse and rat IgGs were purchased from Invitrogen and Thermo Scientific, respectively.The FITC-conjugated secondary antibodies against mouse and rat IgGs were purchased from Invitrogen and Thermo Scientific, respectively.

    Activation Assay:

    Article Title: Anti-Inflammatory and Antimicrobial Effects of Estradiol in Bovine Mammary Epithelial Cells during Staphylococcus aureus Internalization
    Article Snippet: The monoclonal blocking antibodies anti- α 5 β 1 integrin (MAB2514) and anti-TLR2 (TLR2.1) were obtained from Millipore and Abcam, respectively.The monoclonal blocking antibodies anti- α 5 β 1 integrin (MAB2514) and anti-TLR2 (TLR2.1) were obtained from Millipore and Abcam, respectively.. The anti-phospho-ER α (2511S, Ser118) was obtained from Cell Signaling and the anti-ER β (517700) was acquired from Life Technologies.. The FITC-conjugated secondary antibodies against mouse and rat IgGs were purchased from Invitrogen and Thermo Scientific, respectively.The FITC-conjugated secondary antibodies against mouse and rat IgGs were purchased from Invitrogen and Thermo Scientific, respectively.

    Infection:

    Article Title: Anti-Inflammatory and Antimicrobial Effects of Estradiol in Bovine Mammary Epithelial Cells during Staphylococcus aureus Internalization
    Article Snippet: The monoclonal blocking antibodies anti- α 5 β 1 integrin (MAB2514) and anti-TLR2 (TLR2.1) were obtained from Millipore and Abcam, respectively.The monoclonal blocking antibodies anti- α 5 β 1 integrin (MAB2514) and anti-TLR2 (TLR2.1) were obtained from Millipore and Abcam, respectively.. The anti-phospho-ER α (2511S, Ser118) was obtained from Cell Signaling and the anti-ER β (517700) was acquired from Life Technologies.. The FITC-conjugated secondary antibodies against mouse and rat IgGs were purchased from Invitrogen and Thermo Scientific, respectively.The FITC-conjugated secondary antibodies against mouse and rat IgGs were purchased from Invitrogen and Thermo Scientific, respectively.

    Staining:

    Article Title: Anti-Inflammatory and Antimicrobial Effects of Estradiol in Bovine Mammary Epithelial Cells during Staphylococcus aureus Internalization
    Article Snippet: The monoclonal blocking antibodies anti- α 5 β 1 integrin (MAB2514) and anti-TLR2 (TLR2.1) were obtained from Millipore and Abcam, respectively.The monoclonal blocking antibodies anti- α 5 β 1 integrin (MAB2514) and anti-TLR2 (TLR2.1) were obtained from Millipore and Abcam, respectively.. The anti-phospho-ER α (2511S, Ser118) was obtained from Cell Signaling and the anti-ER β (517700) was acquired from Life Technologies.. The FITC-conjugated secondary antibodies against mouse and rat IgGs were purchased from Invitrogen and Thermo Scientific, respectively.The FITC-conjugated secondary antibodies against mouse and rat IgGs were purchased from Invitrogen and Thermo Scientific, respectively.

    Flow Cytometry:

    Article Title: Anti-Inflammatory and Antimicrobial Effects of Estradiol in Bovine Mammary Epithelial Cells during Staphylococcus aureus Internalization
    Article Snippet: The monoclonal blocking antibodies anti- α 5 β 1 integrin (MAB2514) and anti-TLR2 (TLR2.1) were obtained from Millipore and Abcam, respectively.The monoclonal blocking antibodies anti- α 5 β 1 integrin (MAB2514) and anti-TLR2 (TLR2.1) were obtained from Millipore and Abcam, respectively.. The anti-phospho-ER α (2511S, Ser118) was obtained from Cell Signaling and the anti-ER β (517700) was acquired from Life Technologies.. The FITC-conjugated secondary antibodies against mouse and rat IgGs were purchased from Invitrogen and Thermo Scientific, respectively.The FITC-conjugated secondary antibodies against mouse and rat IgGs were purchased from Invitrogen and Thermo Scientific, respectively.

    Expressing:

    Article Title: Anti-Inflammatory and Antimicrobial Effects of Estradiol in Bovine Mammary Epithelial Cells during Staphylococcus aureus Internalization
    Article Snippet: The monoclonal blocking antibodies anti- α 5 β 1 integrin (MAB2514) and anti-TLR2 (TLR2.1) were obtained from Millipore and Abcam, respectively.The monoclonal blocking antibodies anti- α 5 β 1 integrin (MAB2514) and anti-TLR2 (TLR2.1) were obtained from Millipore and Abcam, respectively.. The anti-phospho-ER α (2511S, Ser118) was obtained from Cell Signaling and the anti-ER β (517700) was acquired from Life Technologies.. The FITC-conjugated secondary antibodies against mouse and rat IgGs were purchased from Invitrogen and Thermo Scientific, respectively.The FITC-conjugated secondary antibodies against mouse and rat IgGs were purchased from Invitrogen and Thermo Scientific, respectively.

    Quantitative RT-PCR:

    Article Title: Anti-Inflammatory and Antimicrobial Effects of Estradiol in Bovine Mammary Epithelial Cells during Staphylococcus aureus Internalization
    Article Snippet: The monoclonal blocking antibodies anti- α 5 β 1 integrin (MAB2514) and anti-TLR2 (TLR2.1) were obtained from Millipore and Abcam, respectively.The monoclonal blocking antibodies anti- α 5 β 1 integrin (MAB2514) and anti-TLR2 (TLR2.1) were obtained from Millipore and Abcam, respectively.. The anti-phospho-ER α (2511S, Ser118) was obtained from Cell Signaling and the anti-ER β (517700) was acquired from Life Technologies.. The FITC-conjugated secondary antibodies against mouse and rat IgGs were purchased from Invitrogen and Thermo Scientific, respectively.The FITC-conjugated secondary antibodies against mouse and rat IgGs were purchased from Invitrogen and Thermo Scientific, respectively.



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    phosphorylation er ser118 antibody  (Cell Signaling Technology Inc)
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    a , ER-NTD sequence highlighting charged (negative, light red; positive, light blue) and aromatic residues (light green), with <t>Ser118</t> in red box. b , Top, Kratky plot of SEC-SAXS data (4 °C). Error bars, I ( q ) propagated uncertainties. Bottom, pairwise distance distribution (solid line, SAXS-EOM ; circles, GNOM ; dashed line, flexible-meccano ). c , 1 H- 15 N HSQC spectrum (850 MHz) (see Extended Data Fig. for assignments). d , Secondary structure propensity from 1 H, 15 N and 13 C (C α , C β and C’) chemical shifts using disordered protein algorithm . Low scores indicate minimal structure. e , 15 N amide R 2 / R 1 ratios showing two clusters—cluster I (residues 43–81) and cluster II (108–152)—identified by two-cluster Gaussian fitting . Shaded regions, higher R 2 / R 1 ratios; top, aromatic residues. Error bar, standard deviation propagated from R 1 and R 2 uncertainties. f , Schematic of paramagnetic effect between nitroxide-spin (yellow) and NMR-active nucleus (blue). g , PRE profiles following MTSL spin labelling at six cysteine mutants. Peak intensity ratio ( I para / I dia ) indicates spin label–amide proton distances. Yellow circles, spin label position; dashed lines, predicted random coil effect . I ( q ), normalized scattering intensity; q , scattering vector amplitude.
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    Image Search Results


    a , ER-NTD sequence highlighting charged (negative, light red; positive, light blue) and aromatic residues (light green), with Ser118 in red box. b , Top, Kratky plot of SEC-SAXS data (4 °C). Error bars, I ( q ) propagated uncertainties. Bottom, pairwise distance distribution (solid line, SAXS-EOM ; circles, GNOM ; dashed line, flexible-meccano ). c , 1 H- 15 N HSQC spectrum (850 MHz) (see Extended Data Fig. for assignments). d , Secondary structure propensity from 1 H, 15 N and 13 C (C α , C β and C’) chemical shifts using disordered protein algorithm . Low scores indicate minimal structure. e , 15 N amide R 2 / R 1 ratios showing two clusters—cluster I (residues 43–81) and cluster II (108–152)—identified by two-cluster Gaussian fitting . Shaded regions, higher R 2 / R 1 ratios; top, aromatic residues. Error bar, standard deviation propagated from R 1 and R 2 uncertainties. f , Schematic of paramagnetic effect between nitroxide-spin (yellow) and NMR-active nucleus (blue). g , PRE profiles following MTSL spin labelling at six cysteine mutants. Peak intensity ratio ( I para / I dia ) indicates spin label–amide proton distances. Yellow circles, spin label position; dashed lines, predicted random coil effect . I ( q ), normalized scattering intensity; q , scattering vector amplitude.

    Journal: Nature

    Article Title: The sequence–structure–function relationship of intrinsic ERα disorder

    doi: 10.1038/s41586-024-08400-1

    Figure Lengend Snippet: a , ER-NTD sequence highlighting charged (negative, light red; positive, light blue) and aromatic residues (light green), with Ser118 in red box. b , Top, Kratky plot of SEC-SAXS data (4 °C). Error bars, I ( q ) propagated uncertainties. Bottom, pairwise distance distribution (solid line, SAXS-EOM ; circles, GNOM ; dashed line, flexible-meccano ). c , 1 H- 15 N HSQC spectrum (850 MHz) (see Extended Data Fig. for assignments). d , Secondary structure propensity from 1 H, 15 N and 13 C (C α , C β and C’) chemical shifts using disordered protein algorithm . Low scores indicate minimal structure. e , 15 N amide R 2 / R 1 ratios showing two clusters—cluster I (residues 43–81) and cluster II (108–152)—identified by two-cluster Gaussian fitting . Shaded regions, higher R 2 / R 1 ratios; top, aromatic residues. Error bar, standard deviation propagated from R 1 and R 2 uncertainties. f , Schematic of paramagnetic effect between nitroxide-spin (yellow) and NMR-active nucleus (blue). g , PRE profiles following MTSL spin labelling at six cysteine mutants. Peak intensity ratio ( I para / I dia ) indicates spin label–amide proton distances. Yellow circles, spin label position; dashed lines, predicted random coil effect . I ( q ), normalized scattering intensity; q , scattering vector amplitude.

    Article Snippet: Site-specific phosphorylation at S118 was verified by immunoblot using a phosphorylation-ER Ser118 antibody (Cell Signaling, catalogue no. 2511).

    Techniques: Sequencing, Standard Deviation, Plasmid Preparation

    ( a ) Western blot analysis of purified ER-NTD (WT or S118D) incubated with activated MAPK1/ERK2 kinase, using phospho-Ser118-specific antibody. Total proteins visualized by Ponceau S staining. For gel source data, see Supplementary Fig. . ( b ) GST-Pin1 pulldown assays with purified WT, S118A, or S118D proteins. Pin1, which selectively binds phosphorylated Ser118 , shows robust binding to S118D but not to unphosphorylated or S118A proteins, validating S118D as a phosphomimetic mutation. For gel source data, see Supplementary Fig. .

    Journal: Nature

    Article Title: The sequence–structure–function relationship of intrinsic ERα disorder

    doi: 10.1038/s41586-024-08400-1

    Figure Lengend Snippet: ( a ) Western blot analysis of purified ER-NTD (WT or S118D) incubated with activated MAPK1/ERK2 kinase, using phospho-Ser118-specific antibody. Total proteins visualized by Ponceau S staining. For gel source data, see Supplementary Fig. . ( b ) GST-Pin1 pulldown assays with purified WT, S118A, or S118D proteins. Pin1, which selectively binds phosphorylated Ser118 , shows robust binding to S118D but not to unphosphorylated or S118A proteins, validating S118D as a phosphomimetic mutation. For gel source data, see Supplementary Fig. .

    Article Snippet: Site-specific phosphorylation at S118 was verified by immunoblot using a phosphorylation-ER Ser118 antibody (Cell Signaling, catalogue no. 2511).

    Techniques: Western Blot, Purification, Incubation, Staining, Binding Assay, Mutagenesis