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equilibration buffer  (Bio-Rad)


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    Structured Review

    Bio-Rad equilibration buffer
    Equilibration Buffer, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 97/100, based on 6594 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/equilibration+buffer/Lysis+Buffer/pmc13006527-139-38-36
    Average 97 stars, based on 6594 article reviews
    equilibration buffer - by Bioz Stars, 2026-09
    97/100 stars

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    Related Articles

    Membrane:

    Article Title: Microtubule lattice defects facilitate spastin-mediated severing
    Article Snippet: The cell lysate was then centrifuged for 45 min at 40,000 rpm (190,000 g ) using Type 45 Ti rotor in an Optima XPN-80 ultracentrifuge following the addition of Benzonase (1:10,000, from Sigma Aldrich). .. The supernatant was filtered through a 0.45 μm membrane and subsequently incubated with Ni-NTA agarose beads (160019892, Qiagen) for 2 h. The beads were washed several times in a 10 ml gravity flow column (Econo-Pacchromatography columns, BioRad) with equilibration buffer (Lysis buffer with 30 mM Imidazole) and eluted with equilibration buffer containing 200 mM imidazole. ..

    Article Title: Microtubule lattice defects facilitate spastin-mediated severing.
    Article Snippet: The cell lysate was then centrifuged for 45 min at 40,000 rpm using Type 45 Ti rotor in an Optima XPN-80 ultracentrifuge following the addition of Benzonase (1:10000, from Sigma Aldrich). .. The supernatant was filtered through a 0.45 μm membrane and subsequently incubated with NiNTA agarose beads (160019892, Qiagen) for 2 h. The beads were washed several times in a 10 ml gravity flow column (Econo-Pacchromatography columns, Biorad) with equilibration buffer (Lysis buffer with 30 mM Imidazole) and eluted with equilibration buffer containing 200 mM imidazole. ..

    Incubation:

    Article Title: Microtubule lattice defects facilitate spastin-mediated severing
    Article Snippet: The cell lysate was then centrifuged for 45 min at 40,000 rpm (190,000 g ) using Type 45 Ti rotor in an Optima XPN-80 ultracentrifuge following the addition of Benzonase (1:10,000, from Sigma Aldrich). .. The supernatant was filtered through a 0.45 μm membrane and subsequently incubated with Ni-NTA agarose beads (160019892, Qiagen) for 2 h. The beads were washed several times in a 10 ml gravity flow column (Econo-Pacchromatography columns, BioRad) with equilibration buffer (Lysis buffer with 30 mM Imidazole) and eluted with equilibration buffer containing 200 mM imidazole. ..

    Article Title: Microtubule lattice defects facilitate spastin-mediated severing.
    Article Snippet: The cell lysate was then centrifuged for 45 min at 40,000 rpm using Type 45 Ti rotor in an Optima XPN-80 ultracentrifuge following the addition of Benzonase (1:10000, from Sigma Aldrich). .. The supernatant was filtered through a 0.45 μm membrane and subsequently incubated with NiNTA agarose beads (160019892, Qiagen) for 2 h. The beads were washed several times in a 10 ml gravity flow column (Econo-Pacchromatography columns, Biorad) with equilibration buffer (Lysis buffer with 30 mM Imidazole) and eluted with equilibration buffer containing 200 mM imidazole. ..

    Lysis:

    Article Title: Microtubule lattice defects facilitate spastin-mediated severing
    Article Snippet: The cell lysate was then centrifuged for 45 min at 40,000 rpm (190,000 g ) using Type 45 Ti rotor in an Optima XPN-80 ultracentrifuge following the addition of Benzonase (1:10,000, from Sigma Aldrich). .. The supernatant was filtered through a 0.45 μm membrane and subsequently incubated with Ni-NTA agarose beads (160019892, Qiagen) for 2 h. The beads were washed several times in a 10 ml gravity flow column (Econo-Pacchromatography columns, BioRad) with equilibration buffer (Lysis buffer with 30 mM Imidazole) and eluted with equilibration buffer containing 200 mM imidazole. ..

    Article Title: Microtubule lattice defects facilitate spastin-mediated severing.
    Article Snippet: The cell lysate was then centrifuged for 45 min at 40,000 rpm using Type 45 Ti rotor in an Optima XPN-80 ultracentrifuge following the addition of Benzonase (1:10000, from Sigma Aldrich). .. The supernatant was filtered through a 0.45 μm membrane and subsequently incubated with NiNTA agarose beads (160019892, Qiagen) for 2 h. The beads were washed several times in a 10 ml gravity flow column (Econo-Pacchromatography columns, Biorad) with equilibration buffer (Lysis buffer with 30 mM Imidazole) and eluted with equilibration buffer containing 200 mM imidazole. ..

    Electrofocusing:

    Article Title: A panel of four autoantibodies to tumour-associated antigens in patients with prostate cancer and its potential for multi-cancer detection.
    Article Snippet: .. The focused IEF strips were then equilibrated with equilibration buffer (Bio-Rad, USA) and placed into SDS-PAGE gel to run the second-dimension separation. ..

    Article Title: Exploring Opuntia ficus-indica as a Strategy to Mitigate High Temperatures Effects in Vineyards: Insights into Physiological and Proteomic Responses
    Article Snippet: Isoelectric focusing (IEF) was performed using an IPGphor system (GE Healthcare, Chicago, IL, USA) at 12 ◦C by increasing the voltage in the following steps: 200 v a 1 vh, 200–3500 V until reaching 2800 vh; 3500 V until reaching 10,000 vh; 3500 V until reach‐ ing 5200 vh. .. After IEF, strips were equilibrated for 15 min in equilibration buffer [75 mM Tris‐HCl, pH 8.8; 6 M urea; 29.3% (v/v) glycerol; 2% (w/v) sodium dodecyl sulfate (SDS); and 0.002% bromophenol blue] with 1% (w/v) dithiothreitol (DTT), then replacing DTT by 2.5% iodoacetamide (w/v), followed by separation of proteins based on molecular masses using a 14% polyacrylamide sodium dodecyl sulfate‐polyacrylamide gel electrophoresis (SDS‐PAGE) mini‐gel (Protean xi, Bio‐Rad, Hercules, CA, USA), using the Laemmli buffer system [28]. ..

    Article Title: A panel of four autoantibodies to tumour-associated antigens in patients with prostate cancer and its potential for multi-cancer detection
    Article Snippet: .. The focused IEF strips were then equilibrated with equilibration buffer (Bio-Rad, USA) and placed into SDS-PAGE gel to run the second-dimension separation. ..

    SDS Page:

    Article Title: A panel of four autoantibodies to tumour-associated antigens in patients with prostate cancer and its potential for multi-cancer detection.
    Article Snippet: .. The focused IEF strips were then equilibrated with equilibration buffer (Bio-Rad, USA) and placed into SDS-PAGE gel to run the second-dimension separation. ..

    Article Title: Nuclear Smooth Muscle α-actin Participates in Vascular Smooth Muscle Cell Differentiation
    Article Snippet: Samples were loaded onto 24 cm, pH 4–7, immobilized pH gradient strips (Bio-Rad) overnight and focused in a PROTEAN® i12TM IEF System (Bio-Rad) for 60kVh. .. The strips were equilibrated in Equilibration Buffer I and II (Bio-Rad), the center third parts were cut out and saved, and the strips were gently inserted into a 8-12% SDS-PAGE mini-gel (Bio-Rad). .. The gel was run, transferred to nitrocellulose membrane, blotted with anti-pan actin antibody (MA5-11869, Sigma), and visualized as described in routine immunoblotting.

    Article Title: A panel of four autoantibodies to tumour-associated antigens in patients with prostate cancer and its potential for multi-cancer detection
    Article Snippet: .. The focused IEF strips were then equilibrated with equilibration buffer (Bio-Rad, USA) and placed into SDS-PAGE gel to run the second-dimension separation. ..

    Nucleic Acid Electrophoresis:

    Article Title: Exploring Opuntia ficus-indica as a Strategy to Mitigate High Temperatures Effects in Vineyards: Insights into Physiological and Proteomic Responses
    Article Snippet: Isoelectric focusing (IEF) was performed using an IPGphor system (GE Healthcare, Chicago, IL, USA) at 12 ◦C by increasing the voltage in the following steps: 200 v a 1 vh, 200–3500 V until reaching 2800 vh; 3500 V until reaching 10,000 vh; 3500 V until reach‐ ing 5200 vh. .. After IEF, strips were equilibrated for 15 min in equilibration buffer [75 mM Tris‐HCl, pH 8.8; 6 M urea; 29.3% (v/v) glycerol; 2% (w/v) sodium dodecyl sulfate (SDS); and 0.002% bromophenol blue] with 1% (w/v) dithiothreitol (DTT), then replacing DTT by 2.5% iodoacetamide (w/v), followed by separation of proteins based on molecular masses using a 14% polyacrylamide sodium dodecyl sulfate‐polyacrylamide gel electrophoresis (SDS‐PAGE) mini‐gel (Protean xi, Bio‐Rad, Hercules, CA, USA), using the Laemmli buffer system [28]. ..



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