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casein kinase 2 ck2 substrate motif  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc casein kinase 2 ck2 substrate motif
    FIGURE 2 INTS3 is a <t>CK2</t> substrate. Immunoprecipitation experiment of endogenous INTS3 from lysates of U2OS cells either untreated or exposed to 6 Gy of gamma-irradiation (ionizing radiation; IR). Anti-INTS3 and anti-hSSB1 antibodies were used to assess immunoprecipitated endogenous INTS3 and hSSB1, respectively. CK2 phosphorylation was assessed by probing with an antibody specific for CK2 phosphorylation motifs within substrates. Representative of three independent repeats.
    Casein Kinase 2 Ck2 Substrate Motif, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 95/100, based on 78 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/casein kinase 2 ck2 substrate motif/product/Cell Signaling Technology Inc
    Average 95 stars, based on 78 article reviews
    casein kinase 2 ck2 substrate motif - by Bioz Stars, 2026-02
    95/100 stars

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    1) Product Images from "The molecular details of a novel phosphorylation-dependent interaction between MRN and the SOSS complex."

    Article Title: The molecular details of a novel phosphorylation-dependent interaction between MRN and the SOSS complex.

    Journal: Protein science : a publication of the Protein Society

    doi: 10.1002/pro.4782

    FIGURE 2 INTS3 is a CK2 substrate. Immunoprecipitation experiment of endogenous INTS3 from lysates of U2OS cells either untreated or exposed to 6 Gy of gamma-irradiation (ionizing radiation; IR). Anti-INTS3 and anti-hSSB1 antibodies were used to assess immunoprecipitated endogenous INTS3 and hSSB1, respectively. CK2 phosphorylation was assessed by probing with an antibody specific for CK2 phosphorylation motifs within substrates. Representative of three independent repeats.
    Figure Legend Snippet: FIGURE 2 INTS3 is a CK2 substrate. Immunoprecipitation experiment of endogenous INTS3 from lysates of U2OS cells either untreated or exposed to 6 Gy of gamma-irradiation (ionizing radiation; IR). Anti-INTS3 and anti-hSSB1 antibodies were used to assess immunoprecipitated endogenous INTS3 and hSSB1, respectively. CK2 phosphorylation was assessed by probing with an antibody specific for CK2 phosphorylation motifs within substrates. Representative of three independent repeats.

    Techniques Used: Immunoprecipitation, Irradiation, Phospho-proteomics

    FIGURE 3 Alignment of known CK2-phosphorylation- dependent Nbs1 recognition sites. Sequence alignment of INTS3584–597 with other Nbs1 binding peptides from human MDC1, human CtIP, Schizosaccharomyces pombe Ctp1, and S. pombe Lif1. Sequence alignments were performed using the M-Coffee web server (Moretti et al., 2007). Light and dark gray areas indicate large similarities or sequence conservation, respectively, whereas light blue areas indicate conserved aspartate and glutamate residues.
    Figure Legend Snippet: FIGURE 3 Alignment of known CK2-phosphorylation- dependent Nbs1 recognition sites. Sequence alignment of INTS3584–597 with other Nbs1 binding peptides from human MDC1, human CtIP, Schizosaccharomyces pombe Ctp1, and S. pombe Lif1. Sequence alignments were performed using the M-Coffee web server (Moretti et al., 2007). Light and dark gray areas indicate large similarities or sequence conservation, respectively, whereas light blue areas indicate conserved aspartate and glutamate residues.

    Techniques Used: Phospho-proteomics, Sequencing, Binding Assay



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    FIGURE 2 INTS3 is a <t>CK2</t> substrate. Immunoprecipitation experiment of endogenous INTS3 from lysates of U2OS cells either untreated or exposed to 6 Gy of gamma-irradiation (ionizing radiation; IR). Anti-INTS3 and anti-hSSB1 antibodies were used to assess immunoprecipitated endogenous INTS3 and hSSB1, respectively. CK2 phosphorylation was assessed by probing with an antibody specific for CK2 phosphorylation motifs within substrates. Representative of three independent repeats.
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    FIGURE 2 INTS3 is a <t>CK2</t> substrate. Immunoprecipitation experiment of endogenous INTS3 from lysates of U2OS cells either untreated or exposed to 6 Gy of gamma-irradiation (ionizing radiation; IR). Anti-INTS3 and anti-hSSB1 antibodies were used to assess immunoprecipitated endogenous INTS3 and hSSB1, respectively. CK2 phosphorylation was assessed by probing with an antibody specific for CK2 phosphorylation motifs within substrates. Representative of three independent repeats.
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    Image Search Results


    FIGURE 2 INTS3 is a CK2 substrate. Immunoprecipitation experiment of endogenous INTS3 from lysates of U2OS cells either untreated or exposed to 6 Gy of gamma-irradiation (ionizing radiation; IR). Anti-INTS3 and anti-hSSB1 antibodies were used to assess immunoprecipitated endogenous INTS3 and hSSB1, respectively. CK2 phosphorylation was assessed by probing with an antibody specific for CK2 phosphorylation motifs within substrates. Representative of three independent repeats.

    Journal: Protein science : a publication of the Protein Society

    Article Title: The molecular details of a novel phosphorylation-dependent interaction between MRN and the SOSS complex.

    doi: 10.1002/pro.4782

    Figure Lengend Snippet: FIGURE 2 INTS3 is a CK2 substrate. Immunoprecipitation experiment of endogenous INTS3 from lysates of U2OS cells either untreated or exposed to 6 Gy of gamma-irradiation (ionizing radiation; IR). Anti-INTS3 and anti-hSSB1 antibodies were used to assess immunoprecipitated endogenous INTS3 and hSSB1, respectively. CK2 phosphorylation was assessed by probing with an antibody specific for CK2 phosphorylation motifs within substrates. Representative of three independent repeats.

    Article Snippet: Antibodies against the Casein Kinase 2 (CK2) substrate motif (#8738) were purchased from Cell Signaling Technology (Genesearch).

    Techniques: Immunoprecipitation, Irradiation, Phospho-proteomics

    FIGURE 3 Alignment of known CK2-phosphorylation- dependent Nbs1 recognition sites. Sequence alignment of INTS3584–597 with other Nbs1 binding peptides from human MDC1, human CtIP, Schizosaccharomyces pombe Ctp1, and S. pombe Lif1. Sequence alignments were performed using the M-Coffee web server (Moretti et al., 2007). Light and dark gray areas indicate large similarities or sequence conservation, respectively, whereas light blue areas indicate conserved aspartate and glutamate residues.

    Journal: Protein science : a publication of the Protein Society

    Article Title: The molecular details of a novel phosphorylation-dependent interaction between MRN and the SOSS complex.

    doi: 10.1002/pro.4782

    Figure Lengend Snippet: FIGURE 3 Alignment of known CK2-phosphorylation- dependent Nbs1 recognition sites. Sequence alignment of INTS3584–597 with other Nbs1 binding peptides from human MDC1, human CtIP, Schizosaccharomyces pombe Ctp1, and S. pombe Lif1. Sequence alignments were performed using the M-Coffee web server (Moretti et al., 2007). Light and dark gray areas indicate large similarities or sequence conservation, respectively, whereas light blue areas indicate conserved aspartate and glutamate residues.

    Article Snippet: Antibodies against the Casein Kinase 2 (CK2) substrate motif (#8738) were purchased from Cell Signaling Technology (Genesearch).

    Techniques: Phospho-proteomics, Sequencing, Binding Assay