phosphosafe extraction reagent Search Results


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  • 99
    Millipore phosphosafe extraction reagent cell lysis buffer
    Phosphosafe Extraction Reagent Cell Lysis Buffer, supplied by Millipore, used in various techniques. Bioz Stars score: 99/100, based on 15641 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/phosphosafe extraction reagent cell lysis buffer/product/Millipore
    Average 99 stars, based on 15641 article reviews
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    93
    Millipore phosphosafe extraction reagent
    Agnoprotein is phosphorylated in vivo. (A) Phosphatase-treated agnoprotein exhibits higher signal upon phosphorylation. Whole-cell lysates were prepared from SVG-A cells, transfected with JCV Mad-1 genome, in an extraction buffer supplemented with a <t>PhosphoSafe</t>
    Phosphosafe Extraction Reagent, supplied by Millipore, used in various techniques. Bioz Stars score: 93/100, based on 22 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/phosphosafe extraction reagent/product/Millipore
    Average 93 stars, based on 22 article reviews
    Price from $9.99 to $1999.99
    phosphosafe extraction reagent - by Bioz Stars, 2020-05
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    91
    Thermo Fisher phosphosafe extraction reagent
    Agnoprotein is phosphorylated in vivo. (A) Phosphatase-treated agnoprotein exhibits higher signal upon phosphorylation. Whole-cell lysates were prepared from SVG-A cells, transfected with JCV Mad-1 genome, in an extraction buffer supplemented with a <t>PhosphoSafe</t>
    Phosphosafe Extraction Reagent, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/phosphosafe extraction reagent/product/Thermo Fisher
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    93
    Merck KGaA phosphosafe extraction reagent
    Effect of ASA and/or BTZ treatment on expression of p-AKT in myeloma cells. (A) MM1.S and RPMI-8226 cells were treated with ASA, BTZ and ASA+BTZ for 48 h, respectively, following which the whole cell lysates were prepared using <t>Phosphosafe™</t> extraction reagent. The levels of p-AKT (Thr 308 and Ser 473) and AKT were analyzed using western blot analysis with corresponding antibodies. Each blot is representative of three independent experiments. (B) Integrated optical density data of p-AKT(308) are presented as the mean ± standard deviation. (C) Integrated optical density data of p-AKT(473) are presented as the mean ± standard deviation. *P
    Phosphosafe Extraction Reagent, supplied by Merck KGaA, used in various techniques. Bioz Stars score: 93/100, based on 5 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/phosphosafe extraction reagent/product/Merck KGaA
    Average 93 stars, based on 5 article reviews
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    phosphosafe extraction reagent - by Bioz Stars, 2020-05
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    85
    Merck & Co phosphosafe extraction reagent
    Effect of ASA and/or BTZ treatment on expression of p-AKT in myeloma cells. (A) MM1.S and RPMI-8226 cells were treated with ASA, BTZ and ASA+BTZ for 48 h, respectively, following which the whole cell lysates were prepared using <t>Phosphosafe™</t> extraction reagent. The levels of p-AKT (Thr 308 and Ser 473) and AKT were analyzed using western blot analysis with corresponding antibodies. Each blot is representative of three independent experiments. (B) Integrated optical density data of p-AKT(308) are presented as the mean ± standard deviation. (C) Integrated optical density data of p-AKT(473) are presented as the mean ± standard deviation. *P
    Phosphosafe Extraction Reagent, supplied by Merck & Co, used in various techniques. Bioz Stars score: 85/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Average 85 stars, based on 3 article reviews
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    90
    Millipore phosphosafe extra reagent
    Effect of ASA and/or BTZ treatment on expression of p-AKT in myeloma cells. (A) MM1.S and RPMI-8226 cells were treated with ASA, BTZ and ASA+BTZ for 48 h, respectively, following which the whole cell lysates were prepared using <t>Phosphosafe™</t> extraction reagent. The levels of p-AKT (Thr 308 and Ser 473) and AKT were analyzed using western blot analysis with corresponding antibodies. Each blot is representative of three independent experiments. (B) Integrated optical density data of p-AKT(308) are presented as the mean ± standard deviation. (C) Integrated optical density data of p-AKT(473) are presented as the mean ± standard deviation. *P
    Phosphosafe Extra Reagent, supplied by Millipore, used in various techniques. Bioz Stars score: 90/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    89
    Merck & Co phosphosafe buffer
    Effect of ASA and/or BTZ treatment on expression of p-AKT in myeloma cells. (A) MM1.S and RPMI-8226 cells were treated with ASA, BTZ and ASA+BTZ for 48 h, respectively, following which the whole cell lysates were prepared using <t>Phosphosafe™</t> extraction reagent. The levels of p-AKT (Thr 308 and Ser 473) and AKT were analyzed using western blot analysis with corresponding antibodies. Each blot is representative of three independent experiments. (B) Integrated optical density data of p-AKT(308) are presented as the mean ± standard deviation. (C) Integrated optical density data of p-AKT(473) are presented as the mean ± standard deviation. *P
    Phosphosafe Buffer, supplied by Merck & Co, used in various techniques. Bioz Stars score: 89/100, based on 17 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    99
    Millipore phosstop phosphatase inhibitor
    Effect of ASA and/or BTZ treatment on expression of p-AKT in myeloma cells. (A) MM1.S and RPMI-8226 cells were treated with ASA, BTZ and ASA+BTZ for 48 h, respectively, following which the whole cell lysates were prepared using <t>Phosphosafe™</t> extraction reagent. The levels of p-AKT (Thr 308 and Ser 473) and AKT were analyzed using western blot analysis with corresponding antibodies. Each blot is representative of three independent experiments. (B) Integrated optical density data of p-AKT(308) are presented as the mean ± standard deviation. (C) Integrated optical density data of p-AKT(473) are presented as the mean ± standard deviation. *P
    Phosstop Phosphatase Inhibitor, supplied by Millipore, used in various techniques. Bioz Stars score: 99/100, based on 69 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Image Search Results


    Agnoprotein is phosphorylated in vivo. (A) Phosphatase-treated agnoprotein exhibits higher signal upon phosphorylation. Whole-cell lysates were prepared from SVG-A cells, transfected with JCV Mad-1 genome, in an extraction buffer supplemented with a PhosphoSafe

    Journal:

    Article Title: Phosphorylation Mutants of JC Virus Agnoprotein Are Unable To Sustain the Viral Infection Cycle

    doi: 10.1128/JVI.80.8.3893-3903.2006

    Figure Lengend Snippet: Agnoprotein is phosphorylated in vivo. (A) Phosphatase-treated agnoprotein exhibits higher signal upon phosphorylation. Whole-cell lysates were prepared from SVG-A cells, transfected with JCV Mad-1 genome, in an extraction buffer supplemented with a PhosphoSafe

    Article Snippet: Agnoprotein was immunoprecipitated from whole-cell extracts (200 μg) prepared in an extraction buffer supplemented with a PhosphoSafe extraction reagent (Novagen, catalog no. 71296-3), at 5 or 10 days posttransfection from SVG-A cells transfected with JCV Mad-1 genome and subsequently treated or not treated with alkaline phosphatase (Roche, catalog no. 11097075001) in a 100-μl reaction volume using 80 U of enzyme to remove the phosphate groups from agnoprotein ( ).

    Techniques: In Vivo, Transfection

    Effect of ASA and/or BTZ treatment on expression of p-AKT in myeloma cells. (A) MM1.S and RPMI-8226 cells were treated with ASA, BTZ and ASA+BTZ for 48 h, respectively, following which the whole cell lysates were prepared using Phosphosafe™ extraction reagent. The levels of p-AKT (Thr 308 and Ser 473) and AKT were analyzed using western blot analysis with corresponding antibodies. Each blot is representative of three independent experiments. (B) Integrated optical density data of p-AKT(308) are presented as the mean ± standard deviation. (C) Integrated optical density data of p-AKT(473) are presented as the mean ± standard deviation. *P

    Journal: Oncology Letters

    Article Title: Aspirin enhances the cytotoxic activity of bortezomib against myeloma cells via suppression of Bcl-2, survivin and phosphorylation of AKT

    doi: 10.3892/ol.2016.5472

    Figure Lengend Snippet: Effect of ASA and/or BTZ treatment on expression of p-AKT in myeloma cells. (A) MM1.S and RPMI-8226 cells were treated with ASA, BTZ and ASA+BTZ for 48 h, respectively, following which the whole cell lysates were prepared using Phosphosafe™ extraction reagent. The levels of p-AKT (Thr 308 and Ser 473) and AKT were analyzed using western blot analysis with corresponding antibodies. Each blot is representative of three independent experiments. (B) Integrated optical density data of p-AKT(308) are presented as the mean ± standard deviation. (C) Integrated optical density data of p-AKT(473) are presented as the mean ± standard deviation. *P

    Article Snippet: Phosphosafe™ extraction reagent was purchased from Merck Millipore.

    Techniques: Expressing, Western Blot, Standard Deviation