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Bio-Rad m edta
Protease protection assays for GR A-NTD, GR C2-NTD, and GR C3-NTD. Trypsin digestions were performed at a protein (1 mg/ml):trypsin mass ratio of 1000:1 at 22 °C in 10 m m <t>HEPES,</t> 80 m m NaCl, 1 m m <t>EDTA,</t> 10% glycerol buffer, pH 7.6 for 0, 5, 10,
M Edta, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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1) Product Images from "Thermodynamic Dissection of the Intrinsically Disordered N-terminal Domain of Human Glucocorticoid Receptor *"

Article Title: Thermodynamic Dissection of the Intrinsically Disordered N-terminal Domain of Human Glucocorticoid Receptor *

Journal: The Journal of Biological Chemistry

doi: 10.1074/jbc.M112.355651

Protease protection assays for GR A-NTD, GR C2-NTD, and GR C3-NTD. Trypsin digestions were performed at a protein (1 mg/ml):trypsin mass ratio of 1000:1 at 22 °C in 10 m m HEPES, 80 m m NaCl, 1 m m EDTA, 10% glycerol buffer, pH 7.6 for 0, 5, 10,
Figure Legend Snippet: Protease protection assays for GR A-NTD, GR C2-NTD, and GR C3-NTD. Trypsin digestions were performed at a protein (1 mg/ml):trypsin mass ratio of 1000:1 at 22 °C in 10 m m HEPES, 80 m m NaCl, 1 m m EDTA, 10% glycerol buffer, pH 7.6 for 0, 5, 10,

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    Bio-Rad m edta
    Protease protection assays for GR A-NTD, GR C2-NTD, and GR C3-NTD. Trypsin digestions were performed at a protein (1 mg/ml):trypsin mass ratio of 1000:1 at 22 °C in 10 m m <t>HEPES,</t> 80 m m NaCl, 1 m m <t>EDTA,</t> 10% glycerol buffer, pH 7.6 for 0, 5, 10,
    M Edta, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/m edta/product/Bio-Rad
    Average 99 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    m edta - by Bioz Stars, 2021-05
    99/100 stars
      Buy from Supplier

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    Protease protection assays for GR A-NTD, GR C2-NTD, and GR C3-NTD. Trypsin digestions were performed at a protein (1 mg/ml):trypsin mass ratio of 1000:1 at 22 °C in 10 m m HEPES, 80 m m NaCl, 1 m m EDTA, 10% glycerol buffer, pH 7.6 for 0, 5, 10,

    Journal: The Journal of Biological Chemistry

    Article Title: Thermodynamic Dissection of the Intrinsically Disordered N-terminal Domain of Human Glucocorticoid Receptor *

    doi: 10.1074/jbc.M112.355651

    Figure Lengend Snippet: Protease protection assays for GR A-NTD, GR C2-NTD, and GR C3-NTD. Trypsin digestions were performed at a protein (1 mg/ml):trypsin mass ratio of 1000:1 at 22 °C in 10 m m HEPES, 80 m m NaCl, 1 m m EDTA, 10% glycerol buffer, pH 7.6 for 0, 5, 10,

    Article Snippet: Digestions were performed at a protein:trypsin mass ratio of 1000:1 in 10 m m HEPES, 80 m m NaCl, 1 m m EDTA, 10% glycerol buffer, pH 7.6 for 0, 5, 10, and 30 min. Digestions were quenched by mixing the protein and trypsin mixture with 6× Laemmli sample buffer and boiling at 100 °C for 10 min. A 40-μg sample at each time point was separated on 4–15% Tris-HCl gel (Bio-Rad) with SDS-Tris-glycine gel running buffer.

    Techniques: