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purified pp2a-ac dimer  (Millipore)


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    Millipore purified pp2a-ac dimer
    Purified Pp2a Ac Dimer, supplied by Millipore, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/pp2a+dimer/pp2a+immunoprecipitation+phosphatase+assay+kit/pmc05354324-500-9-13
    Average 90 stars, based on 1 article reviews
    purified pp2a-ac dimer - by Bioz Stars, 2026-09
    90/100 stars

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    Related Articles

    Purification:

    Article Title: A Phosphorylation Switch Regulates the Transcriptional Activation of Cell Cycle Regulator p21 by Histone Deacetylase Inhibitors
    Article Snippet: Phosphatase reactions were carried out by adding 0.5 units of PP2A A/C dimer (Millipore Upstate Biotechnology) for 2 h at 30 °C.

    Article Title: ARPP-16 Is a Striatal-Enriched Inhibitor of Protein Phosphatase 2A Regulated by Microtubule-Associated Serine/Threonine Kinase 3 (Mast 3 Kinase)
    Article Snippet: ARPP-16 inhibits PP2A activity in vitro . a , Purified PP2A-AC dimer (0.01 U/μl, Millipore) was incubated with increasing concentration (0, 0.05, 0.1, and 1 μ m ) of recombinant, purified dephospho-ARPP-16 (top) or P-γ-Ser46-ARPP-16 (bottom) for 10 min at 37°C and phosphatase activity measured using 500 μ m phosphopeptide as substrate.

    Article Title: Evidence toward a Dual Phosphatase Mechanism That Restricts Aurora A (Thr-295) Phosphorylation during the Early Embryonic Cell Cycle
    Article Snippet: MBP-dEnsa (S68D) was used at 10 or 30 μ m , and αPP1-C (New England Biolabs) and PP2A-A/C dimer (Millipore, lot number 2044810) were used at 0.012 units/μl.

    Article Title: Recurrent PPP2R1A Mutations in Uterine Cancer Act through a Dominant-Negative Mechanism to Promote Malignant Cell Growth
    Article Snippet: 20μl of this ‘phosphatase suspension’ or 20μl of a 1/80 dilution of purified PP2A dimer (0.1Unit/μl, Millipore) was incubated with 9μl of 2mM stock of R-R-A-pT-V-A phosphopeptide for 10-60 minutes at 30°C (in the linear range of the assay).

    Article Title: ARPP-16 Is a Striatal-Enriched Inhibitor of Protein Phosphatase 2A Regulated by Microtubule-Associated Serine/Threonine Kinase 3 (Mast 3 Kinase)
    Article Snippet: Immunocomplexes for Bα-, B56δ-, or PR72-PP2A trimers or purified PP2A-AC dimer (0.01 U/μl, Millipore) were resuspended in 100 μl of PP2A reaction buffer and incubated without or with ARPP-16 or thio-γ-phosphorylated ARPP-16 (50 n m , 100 n m , 1000 n m ) for 10 min at 37°C in the presence of 500 μ m phosphopeptide (K-R-pT-I-R-R).

    Article Title: Evidence toward a Dual Phosphatase Mechanism That Restricts Aurora A (Thr-295) Phosphorylation during the Early Embryonic Cell Cycle
    Article Snippet: In vitro phosphatase assays were performed by incubating 120 ng of recombinant His-tagged Xenopus AurA with protein phosphatase dilution buffer (Millipore) alone, 2.5 units of αPP1-C (New England Biolabs) or PP2A-A/C dimer (Millipore) in a 20-μl reaction volume.

    Incubation:

    Article Title: A Phosphorylation Switch Regulates the Transcriptional Activation of Cell Cycle Regulator p21 by Histone Deacetylase Inhibitors
    Article Snippet: Phosphatase reactions were carried out by adding 0.5 units of PP2A A/C dimer (Millipore Upstate Biotechnology) for 2 h at 30 °C.

    Article Title: ARPP-16 Is a Striatal-Enriched Inhibitor of Protein Phosphatase 2A Regulated by Microtubule-Associated Serine/Threonine Kinase 3 (Mast 3 Kinase)
    Article Snippet: ARPP-16 inhibits PP2A activity in vitro . a , Purified PP2A-AC dimer (0.01 U/μl, Millipore) was incubated with increasing concentration (0, 0.05, 0.1, and 1 μ m ) of recombinant, purified dephospho-ARPP-16 (top) or P-γ-Ser46-ARPP-16 (bottom) for 10 min at 37°C and phosphatase activity measured using 500 μ m phosphopeptide as substrate.

    Article Title: Evidence toward a Dual Phosphatase Mechanism That Restricts Aurora A (Thr-295) Phosphorylation during the Early Embryonic Cell Cycle
    Article Snippet: MBP-dEnsa (S68D) was used at 10 or 30 μ m , and αPP1-C (New England Biolabs) and PP2A-A/C dimer (Millipore, lot number 2044810) were used at 0.012 units/μl.

    Article Title: Recurrent PPP2R1A Mutations in Uterine Cancer Act through a Dominant-Negative Mechanism to Promote Malignant Cell Growth
    Article Snippet: 20μl of this ‘phosphatase suspension’ or 20μl of a 1/80 dilution of purified PP2A dimer (0.1Unit/μl, Millipore) was incubated with 9μl of 2mM stock of R-R-A-pT-V-A phosphopeptide for 10-60 minutes at 30°C (in the linear range of the assay).

    Article Title: ARPP-16 Is a Striatal-Enriched Inhibitor of Protein Phosphatase 2A Regulated by Microtubule-Associated Serine/Threonine Kinase 3 (Mast 3 Kinase)
    Article Snippet: Immunocomplexes for Bα-, B56δ-, or PR72-PP2A trimers or purified PP2A-AC dimer (0.01 U/μl, Millipore) were resuspended in 100 μl of PP2A reaction buffer and incubated without or with ARPP-16 or thio-γ-phosphorylated ARPP-16 (50 n m , 100 n m , 1000 n m ) for 10 min at 37°C in the presence of 500 μ m phosphopeptide (K-R-pT-I-R-R).

    Article Title: Evidence toward a Dual Phosphatase Mechanism That Restricts Aurora A (Thr-295) Phosphorylation during the Early Embryonic Cell Cycle
    Article Snippet: In vitro phosphatase assays were performed by incubating 120 ng of recombinant His-tagged Xenopus AurA with protein phosphatase dilution buffer (Millipore) alone, 2.5 units of αPP1-C (New England Biolabs) or PP2A-A/C dimer (Millipore) in a 20-μl reaction volume.

    Phospho-proteomics:

    Article Title: A Phosphorylation Switch Regulates the Transcriptional Activation of Cell Cycle Regulator p21 by Histone Deacetylase Inhibitors
    Article Snippet: Phosphatase reactions were carried out by adding 0.5 units of PP2A A/C dimer (Millipore Upstate Biotechnology) for 2 h at 30 °C.

    Article Title: ARPP-16 Is a Striatal-Enriched Inhibitor of Protein Phosphatase 2A Regulated by Microtubule-Associated Serine/Threonine Kinase 3 (Mast 3 Kinase)
    Article Snippet: ARPP-16 inhibits PP2A activity in vitro . a , Purified PP2A-AC dimer (0.01 U/μl, Millipore) was incubated with increasing concentration (0, 0.05, 0.1, and 1 μ m ) of recombinant, purified dephospho-ARPP-16 (top) or P-γ-Ser46-ARPP-16 (bottom) for 10 min at 37°C and phosphatase activity measured using 500 μ m phosphopeptide as substrate.

    Article Title: Evidence toward a Dual Phosphatase Mechanism That Restricts Aurora A (Thr-295) Phosphorylation during the Early Embryonic Cell Cycle
    Article Snippet: MBP-dEnsa (S68D) was used at 10 or 30 μ m , and αPP1-C (New England Biolabs) and PP2A-A/C dimer (Millipore, lot number 2044810) were used at 0.012 units/μl.

    Article Title: Recurrent PPP2R1A Mutations in Uterine Cancer Act through a Dominant-Negative Mechanism to Promote Malignant Cell Growth
    Article Snippet: 20μl of this ‘phosphatase suspension’ or 20μl of a 1/80 dilution of purified PP2A dimer (0.1Unit/μl, Millipore) was incubated with 9μl of 2mM stock of R-R-A-pT-V-A phosphopeptide for 10-60 minutes at 30°C (in the linear range of the assay).

    Article Title: ARPP-16 Is a Striatal-Enriched Inhibitor of Protein Phosphatase 2A Regulated by Microtubule-Associated Serine/Threonine Kinase 3 (Mast 3 Kinase)
    Article Snippet: Immunocomplexes for Bα-, B56δ-, or PR72-PP2A trimers or purified PP2A-AC dimer (0.01 U/μl, Millipore) were resuspended in 100 μl of PP2A reaction buffer and incubated without or with ARPP-16 or thio-γ-phosphorylated ARPP-16 (50 n m , 100 n m , 1000 n m ) for 10 min at 37°C in the presence of 500 μ m phosphopeptide (K-R-pT-I-R-R).

    Article Title: Evidence toward a Dual Phosphatase Mechanism That Restricts Aurora A (Thr-295) Phosphorylation during the Early Embryonic Cell Cycle
    Article Snippet: In vitro phosphatase assays were performed by incubating 120 ng of recombinant His-tagged Xenopus AurA with protein phosphatase dilution buffer (Millipore) alone, 2.5 units of αPP1-C (New England Biolabs) or PP2A-A/C dimer (Millipore) in a 20-μl reaction volume.

    Activity Assay:

    Article Title: A Phosphorylation Switch Regulates the Transcriptional Activation of Cell Cycle Regulator p21 by Histone Deacetylase Inhibitors
    Article Snippet: Phosphatase reactions were carried out by adding 0.5 units of PP2A A/C dimer (Millipore Upstate Biotechnology) for 2 h at 30 °C.

    Article Title: ARPP-16 Is a Striatal-Enriched Inhibitor of Protein Phosphatase 2A Regulated by Microtubule-Associated Serine/Threonine Kinase 3 (Mast 3 Kinase)
    Article Snippet: ARPP-16 inhibits PP2A activity in vitro . a , Purified PP2A-AC dimer (0.01 U/μl, Millipore) was incubated with increasing concentration (0, 0.05, 0.1, and 1 μ m ) of recombinant, purified dephospho-ARPP-16 (top) or P-γ-Ser46-ARPP-16 (bottom) for 10 min at 37°C and phosphatase activity measured using 500 μ m phosphopeptide as substrate.

    Article Title: Evidence toward a Dual Phosphatase Mechanism That Restricts Aurora A (Thr-295) Phosphorylation during the Early Embryonic Cell Cycle
    Article Snippet: MBP-dEnsa (S68D) was used at 10 or 30 μ m , and αPP1-C (New England Biolabs) and PP2A-A/C dimer (Millipore, lot number 2044810) were used at 0.012 units/μl.

    Article Title: Recurrent PPP2R1A Mutations in Uterine Cancer Act through a Dominant-Negative Mechanism to Promote Malignant Cell Growth
    Article Snippet: 20μl of this ‘phosphatase suspension’ or 20μl of a 1/80 dilution of purified PP2A dimer (0.1Unit/μl, Millipore) was incubated with 9μl of 2mM stock of R-R-A-pT-V-A phosphopeptide for 10-60 minutes at 30°C (in the linear range of the assay).

    Article Title: ARPP-16 Is a Striatal-Enriched Inhibitor of Protein Phosphatase 2A Regulated by Microtubule-Associated Serine/Threonine Kinase 3 (Mast 3 Kinase)
    Article Snippet: Immunocomplexes for Bα-, B56δ-, or PR72-PP2A trimers or purified PP2A-AC dimer (0.01 U/μl, Millipore) were resuspended in 100 μl of PP2A reaction buffer and incubated without or with ARPP-16 or thio-γ-phosphorylated ARPP-16 (50 n m , 100 n m , 1000 n m ) for 10 min at 37°C in the presence of 500 μ m phosphopeptide (K-R-pT-I-R-R).

    Article Title: Evidence toward a Dual Phosphatase Mechanism That Restricts Aurora A (Thr-295) Phosphorylation during the Early Embryonic Cell Cycle
    Article Snippet: In vitro phosphatase assays were performed by incubating 120 ng of recombinant His-tagged Xenopus AurA with protein phosphatase dilution buffer (Millipore) alone, 2.5 units of αPP1-C (New England Biolabs) or PP2A-A/C dimer (Millipore) in a 20-μl reaction volume.

    In Vitro:

    Article Title: A Phosphorylation Switch Regulates the Transcriptional Activation of Cell Cycle Regulator p21 by Histone Deacetylase Inhibitors
    Article Snippet: Phosphatase reactions were carried out by adding 0.5 units of PP2A A/C dimer (Millipore Upstate Biotechnology) for 2 h at 30 °C.

    Article Title: ARPP-16 Is a Striatal-Enriched Inhibitor of Protein Phosphatase 2A Regulated by Microtubule-Associated Serine/Threonine Kinase 3 (Mast 3 Kinase)
    Article Snippet: ARPP-16 inhibits PP2A activity in vitro . a , Purified PP2A-AC dimer (0.01 U/μl, Millipore) was incubated with increasing concentration (0, 0.05, 0.1, and 1 μ m ) of recombinant, purified dephospho-ARPP-16 (top) or P-γ-Ser46-ARPP-16 (bottom) for 10 min at 37°C and phosphatase activity measured using 500 μ m phosphopeptide as substrate.

    Article Title: Evidence toward a Dual Phosphatase Mechanism That Restricts Aurora A (Thr-295) Phosphorylation during the Early Embryonic Cell Cycle
    Article Snippet: MBP-dEnsa (S68D) was used at 10 or 30 μ m , and αPP1-C (New England Biolabs) and PP2A-A/C dimer (Millipore, lot number 2044810) were used at 0.012 units/μl.

    Article Title: Recurrent PPP2R1A Mutations in Uterine Cancer Act through a Dominant-Negative Mechanism to Promote Malignant Cell Growth
    Article Snippet: 20μl of this ‘phosphatase suspension’ or 20μl of a 1/80 dilution of purified PP2A dimer (0.1Unit/μl, Millipore) was incubated with 9μl of 2mM stock of R-R-A-pT-V-A phosphopeptide for 10-60 minutes at 30°C (in the linear range of the assay).

    Article Title: ARPP-16 Is a Striatal-Enriched Inhibitor of Protein Phosphatase 2A Regulated by Microtubule-Associated Serine/Threonine Kinase 3 (Mast 3 Kinase)
    Article Snippet: Immunocomplexes for Bα-, B56δ-, or PR72-PP2A trimers or purified PP2A-AC dimer (0.01 U/μl, Millipore) were resuspended in 100 μl of PP2A reaction buffer and incubated without or with ARPP-16 or thio-γ-phosphorylated ARPP-16 (50 n m , 100 n m , 1000 n m ) for 10 min at 37°C in the presence of 500 μ m phosphopeptide (K-R-pT-I-R-R).

    Article Title: Evidence toward a Dual Phosphatase Mechanism That Restricts Aurora A (Thr-295) Phosphorylation during the Early Embryonic Cell Cycle
    Article Snippet: In vitro phosphatase assays were performed by incubating 120 ng of recombinant His-tagged Xenopus AurA with protein phosphatase dilution buffer (Millipore) alone, 2.5 units of αPP1-C (New England Biolabs) or PP2A-A/C dimer (Millipore) in a 20-μl reaction volume.

    Concentration Assay:

    Article Title: A Phosphorylation Switch Regulates the Transcriptional Activation of Cell Cycle Regulator p21 by Histone Deacetylase Inhibitors
    Article Snippet: Phosphatase reactions were carried out by adding 0.5 units of PP2A A/C dimer (Millipore Upstate Biotechnology) for 2 h at 30 °C.

    Article Title: ARPP-16 Is a Striatal-Enriched Inhibitor of Protein Phosphatase 2A Regulated by Microtubule-Associated Serine/Threonine Kinase 3 (Mast 3 Kinase)
    Article Snippet: ARPP-16 inhibits PP2A activity in vitro . a , Purified PP2A-AC dimer (0.01 U/μl, Millipore) was incubated with increasing concentration (0, 0.05, 0.1, and 1 μ m ) of recombinant, purified dephospho-ARPP-16 (top) or P-γ-Ser46-ARPP-16 (bottom) for 10 min at 37°C and phosphatase activity measured using 500 μ m phosphopeptide as substrate.

    Article Title: Evidence toward a Dual Phosphatase Mechanism That Restricts Aurora A (Thr-295) Phosphorylation during the Early Embryonic Cell Cycle
    Article Snippet: MBP-dEnsa (S68D) was used at 10 or 30 μ m , and αPP1-C (New England Biolabs) and PP2A-A/C dimer (Millipore, lot number 2044810) were used at 0.012 units/μl.

    Article Title: Recurrent PPP2R1A Mutations in Uterine Cancer Act through a Dominant-Negative Mechanism to Promote Malignant Cell Growth
    Article Snippet: 20μl of this ‘phosphatase suspension’ or 20μl of a 1/80 dilution of purified PP2A dimer (0.1Unit/μl, Millipore) was incubated with 9μl of 2mM stock of R-R-A-pT-V-A phosphopeptide for 10-60 minutes at 30°C (in the linear range of the assay).

    Article Title: ARPP-16 Is a Striatal-Enriched Inhibitor of Protein Phosphatase 2A Regulated by Microtubule-Associated Serine/Threonine Kinase 3 (Mast 3 Kinase)
    Article Snippet: Immunocomplexes for Bα-, B56δ-, or PR72-PP2A trimers or purified PP2A-AC dimer (0.01 U/μl, Millipore) were resuspended in 100 μl of PP2A reaction buffer and incubated without or with ARPP-16 or thio-γ-phosphorylated ARPP-16 (50 n m , 100 n m , 1000 n m ) for 10 min at 37°C in the presence of 500 μ m phosphopeptide (K-R-pT-I-R-R).

    Article Title: Evidence toward a Dual Phosphatase Mechanism That Restricts Aurora A (Thr-295) Phosphorylation during the Early Embryonic Cell Cycle
    Article Snippet: In vitro phosphatase assays were performed by incubating 120 ng of recombinant His-tagged Xenopus AurA with protein phosphatase dilution buffer (Millipore) alone, 2.5 units of αPP1-C (New England Biolabs) or PP2A-A/C dimer (Millipore) in a 20-μl reaction volume.

    Recombinant:

    Article Title: A Phosphorylation Switch Regulates the Transcriptional Activation of Cell Cycle Regulator p21 by Histone Deacetylase Inhibitors
    Article Snippet: Phosphatase reactions were carried out by adding 0.5 units of PP2A A/C dimer (Millipore Upstate Biotechnology) for 2 h at 30 °C.

    Article Title: ARPP-16 Is a Striatal-Enriched Inhibitor of Protein Phosphatase 2A Regulated by Microtubule-Associated Serine/Threonine Kinase 3 (Mast 3 Kinase)
    Article Snippet: ARPP-16 inhibits PP2A activity in vitro . a , Purified PP2A-AC dimer (0.01 U/μl, Millipore) was incubated with increasing concentration (0, 0.05, 0.1, and 1 μ m ) of recombinant, purified dephospho-ARPP-16 (top) or P-γ-Ser46-ARPP-16 (bottom) for 10 min at 37°C and phosphatase activity measured using 500 μ m phosphopeptide as substrate.

    Article Title: Evidence toward a Dual Phosphatase Mechanism That Restricts Aurora A (Thr-295) Phosphorylation during the Early Embryonic Cell Cycle
    Article Snippet: MBP-dEnsa (S68D) was used at 10 or 30 μ m , and αPP1-C (New England Biolabs) and PP2A-A/C dimer (Millipore, lot number 2044810) were used at 0.012 units/μl.

    Article Title: Recurrent PPP2R1A Mutations in Uterine Cancer Act through a Dominant-Negative Mechanism to Promote Malignant Cell Growth
    Article Snippet: 20μl of this ‘phosphatase suspension’ or 20μl of a 1/80 dilution of purified PP2A dimer (0.1Unit/μl, Millipore) was incubated with 9μl of 2mM stock of R-R-A-pT-V-A phosphopeptide for 10-60 minutes at 30°C (in the linear range of the assay).

    Article Title: ARPP-16 Is a Striatal-Enriched Inhibitor of Protein Phosphatase 2A Regulated by Microtubule-Associated Serine/Threonine Kinase 3 (Mast 3 Kinase)
    Article Snippet: Immunocomplexes for Bα-, B56δ-, or PR72-PP2A trimers or purified PP2A-AC dimer (0.01 U/μl, Millipore) were resuspended in 100 μl of PP2A reaction buffer and incubated without or with ARPP-16 or thio-γ-phosphorylated ARPP-16 (50 n m , 100 n m , 1000 n m ) for 10 min at 37°C in the presence of 500 μ m phosphopeptide (K-R-pT-I-R-R).

    Article Title: Evidence toward a Dual Phosphatase Mechanism That Restricts Aurora A (Thr-295) Phosphorylation during the Early Embryonic Cell Cycle
    Article Snippet: In vitro phosphatase assays were performed by incubating 120 ng of recombinant His-tagged Xenopus AurA with protein phosphatase dilution buffer (Millipore) alone, 2.5 units of αPP1-C (New England Biolabs) or PP2A-A/C dimer (Millipore) in a 20-μl reaction volume.

    Suspension:

    Article Title: A Phosphorylation Switch Regulates the Transcriptional Activation of Cell Cycle Regulator p21 by Histone Deacetylase Inhibitors
    Article Snippet: Phosphatase reactions were carried out by adding 0.5 units of PP2A A/C dimer (Millipore Upstate Biotechnology) for 2 h at 30 °C.

    Article Title: ARPP-16 Is a Striatal-Enriched Inhibitor of Protein Phosphatase 2A Regulated by Microtubule-Associated Serine/Threonine Kinase 3 (Mast 3 Kinase)
    Article Snippet: ARPP-16 inhibits PP2A activity in vitro . a , Purified PP2A-AC dimer (0.01 U/μl, Millipore) was incubated with increasing concentration (0, 0.05, 0.1, and 1 μ m ) of recombinant, purified dephospho-ARPP-16 (top) or P-γ-Ser46-ARPP-16 (bottom) for 10 min at 37°C and phosphatase activity measured using 500 μ m phosphopeptide as substrate.

    Article Title: Evidence toward a Dual Phosphatase Mechanism That Restricts Aurora A (Thr-295) Phosphorylation during the Early Embryonic Cell Cycle
    Article Snippet: MBP-dEnsa (S68D) was used at 10 or 30 μ m , and αPP1-C (New England Biolabs) and PP2A-A/C dimer (Millipore, lot number 2044810) were used at 0.012 units/μl.

    Article Title: Recurrent PPP2R1A Mutations in Uterine Cancer Act through a Dominant-Negative Mechanism to Promote Malignant Cell Growth
    Article Snippet: 20μl of this ‘phosphatase suspension’ or 20μl of a 1/80 dilution of purified PP2A dimer (0.1Unit/μl, Millipore) was incubated with 9μl of 2mM stock of R-R-A-pT-V-A phosphopeptide for 10-60 minutes at 30°C (in the linear range of the assay).

    Article Title: ARPP-16 Is a Striatal-Enriched Inhibitor of Protein Phosphatase 2A Regulated by Microtubule-Associated Serine/Threonine Kinase 3 (Mast 3 Kinase)
    Article Snippet: Immunocomplexes for Bα-, B56δ-, or PR72-PP2A trimers or purified PP2A-AC dimer (0.01 U/μl, Millipore) were resuspended in 100 μl of PP2A reaction buffer and incubated without or with ARPP-16 or thio-γ-phosphorylated ARPP-16 (50 n m , 100 n m , 1000 n m ) for 10 min at 37°C in the presence of 500 μ m phosphopeptide (K-R-pT-I-R-R).

    Article Title: Evidence toward a Dual Phosphatase Mechanism That Restricts Aurora A (Thr-295) Phosphorylation during the Early Embryonic Cell Cycle
    Article Snippet: In vitro phosphatase assays were performed by incubating 120 ng of recombinant His-tagged Xenopus AurA with protein phosphatase dilution buffer (Millipore) alone, 2.5 units of αPP1-C (New England Biolabs) or PP2A-A/C dimer (Millipore) in a 20-μl reaction volume.



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