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restore plus western blot stripping buffer  (Thermo Fisher)


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    Structured Review

    Thermo Fisher restore plus western blot stripping buffer
    Restore Plus Western Blot Stripping Buffer, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/restore+plus+western+blot+stripping+buffer/Semi+dry+blot+transfer+buffer/pm41549045-106-5-11
    Average 96 stars, based on 1 article reviews
    restore plus western blot stripping buffer - by Bioz Stars, 2026-10
    96/100 stars

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    Related Articles

    Membrane:

    Article Title: Proximity Labeling of NIMA Kinase Complex Components in C. elegans
    Article Snippet: .. The resulting blot was imaged, and the membrane was then washed with 1× TBS buffer for 30 seconds and was stripped using Restore PLUS Western Blot Stripping Buffer (Thermo Fisher Scientific, Cat# 46430) for 30 minutes at 37°C with shaking. ..

    Article Title: Supporting Information for Presynaptic neurons self-tune by inversely coupling neurotransmitter release with the abundance of CaV2 voltage-gated Ca2+ channels
    Article Snippet: The PVDF membrane was probed with primary mouse monoclonal anti-ubiquitin antibody (Santa Cruz Biotechnology, sc-8017; WB 1:1,000) and secondary HRP-linked anti-mouse IgG (Cell Signaling Technology, cat# 7076S; WB 1:10,000). .. The PVDF membrane was then stripped with Restore PLUS Western Blot Stripping Buffer (ThermoFisher Scientific, cat# 46430) for 15 minutes. .. The membrane was then probed with primary rabbit monoclonal anti-GFP antibody (Cell Signaling Technology, cat# 2956S WB 1:1,000) and HRP-linked anti-rabbit IgG (Cell Signaling Technology, cat# 7074S WB 1:10,000).

    Article Title: Phenotypic screens for SIRPA expression reveal RAB21 as a general regulator of macrophage surface identity.
    Article Snippet: Flow cytometry-based detection of total CD47 and CD47pyroGlu expression in cells treated with the QPCTL inhibitor SEN177 HAP1, Ramos, THP-1, and U-937 cells were seeded in 96-well plates and treated with a 9-point serial dilution of SEN177 (SigmaAldrich, #SML1615) from 50 μM to 7.6 nM for 72 h. The final volume per well was 100 μL, with 8,000 cells for HAP1, 10,000 for Ramos, 15,000 for U-937, and 30,000 for THP-1. .. After imaging, the IP membrane was stripped with Restore PLUS Western Blot Stripping Buffer (Thermo Scientific, #46430) and blocked, followed by probing with anti-Sirpa antibody, secondary antibody incubation, imaging, and processing as indicated in the ‘‘Western blot detection of total Sirpa levels in RAW264.7 lines’’ section. .. Flow cytometry-based detection of total CD47 and CD47pyroGlu expression in cells treated with the QPCTL inhibitor SEN177 HAP1, Ramos, THP-1, and U-937 cells were seeded in 96-well plates and treated with a 9-point serial dilution of SEN177 (SigmaAldrich, #SML1615) from 50 μM to 7.6 nM for 72 h. The final volume per well was 100 μL, with 8,000 cells for HAP1, 10,000 for Ramos, 15,000 for U-937, and 30,000 for THP-1.

    Western Blot:

    Article Title: Proximity Labeling of NIMA Kinase Complex Components in C. elegans
    Article Snippet: .. The resulting blot was imaged, and the membrane was then washed with 1× TBS buffer for 30 seconds and was stripped using Restore PLUS Western Blot Stripping Buffer (Thermo Fisher Scientific, Cat# 46430) for 30 minutes at 37°C with shaking. ..

    Article Title: Supporting Information for Presynaptic neurons self-tune by inversely coupling neurotransmitter release with the abundance of CaV2 voltage-gated Ca2+ channels
    Article Snippet: The PVDF membrane was probed with primary mouse monoclonal anti-ubiquitin antibody (Santa Cruz Biotechnology, sc-8017; WB 1:1,000) and secondary HRP-linked anti-mouse IgG (Cell Signaling Technology, cat# 7076S; WB 1:10,000). .. The PVDF membrane was then stripped with Restore PLUS Western Blot Stripping Buffer (ThermoFisher Scientific, cat# 46430) for 15 minutes. .. The membrane was then probed with primary rabbit monoclonal anti-GFP antibody (Cell Signaling Technology, cat# 2956S WB 1:1,000) and HRP-linked anti-rabbit IgG (Cell Signaling Technology, cat# 7074S WB 1:10,000).

    Article Title: IMPDH inhibition induces DNA replication stress and ATR sensitivity in Merkel cell carcinoma
    Article Snippet: .. For blots that were reblotted, blots were washed with TBST once and then stripped by incubation with Restore PLUS western blot stripping buffer (Thermo Scientific) for 10 min. Blots were then washed three times with TBST and blocked with 5% milk in TBST for 1 h at room temperature. ..

    Article Title: Phenotypic screens for SIRPA expression reveal RAB21 as a general regulator of macrophage surface identity.
    Article Snippet: Flow cytometry-based detection of total CD47 and CD47pyroGlu expression in cells treated with the QPCTL inhibitor SEN177 HAP1, Ramos, THP-1, and U-937 cells were seeded in 96-well plates and treated with a 9-point serial dilution of SEN177 (SigmaAldrich, #SML1615) from 50 μM to 7.6 nM for 72 h. The final volume per well was 100 μL, with 8,000 cells for HAP1, 10,000 for Ramos, 15,000 for U-937, and 30,000 for THP-1. .. After imaging, the IP membrane was stripped with Restore PLUS Western Blot Stripping Buffer (Thermo Scientific, #46430) and blocked, followed by probing with anti-Sirpa antibody, secondary antibody incubation, imaging, and processing as indicated in the ‘‘Western blot detection of total Sirpa levels in RAW264.7 lines’’ section. .. Flow cytometry-based detection of total CD47 and CD47pyroGlu expression in cells treated with the QPCTL inhibitor SEN177 HAP1, Ramos, THP-1, and U-937 cells were seeded in 96-well plates and treated with a 9-point serial dilution of SEN177 (SigmaAldrich, #SML1615) from 50 μM to 7.6 nM for 72 h. The final volume per well was 100 μL, with 8,000 cells for HAP1, 10,000 for Ramos, 15,000 for U-937, and 30,000 for THP-1.

    Article Title: Bruton tyrosine kinase (Btk) in neutrophils is indispensable for initiating and maintaining skin inflammation in a model of pemphigoid diseases.
    Article Snippet: Afterwards, membranes were incubated with rabbit anti-Btk (D3H5; Cell Signaling Technology, Danvers, MA, USA; RRID: AB_10950506) over night and subsequently with horseradish peroxidase-labelled polyclonal goat anti-rabbit (Agilent, Santa Clara, CA, USA; RRID: AB_2617138) for 60 min. Membranes were developed using Clarity Western ECL substrate (BioRad, Feldkirchen, Germany). .. Afterwards, membranes were stripped using Restore Plus Western blot stripping buffer (Thermo Fisher Scientific) according to the manufacturer's instructions, blocked with 5% BSA in TBS-T for 1 h and reprobed with rabbit anti-β-actin (13E5; Cell Signalling Technology; RRID: AB_2223172) and subsequently with HRP-labelled polyclonal goat anti-rabbit for 1 h before developed with ECL substrate. ..

    Article Title: TUG protein acts through a disordered region to organize the early secretory pathway.
    Article Snippet: Control and floxed MEFs were treated withAd5CMVCre (Ad-Cre), an adenovirus containingCre recombinase, which was purchased from the Gene Transfer Vector Core at the University of Iowa. .. For re-probing themembranes using adifferent primaryantibody, membranes were stripped using the Restore PLUS western blot stripping buffer (Thermo Fischer Scientific) for 15min at room temperature. ..

    Article Title: TUG protein acts through a disordered region to organize the early secretory pathway
    Article Snippet: Proteins were detected using chemiluminescence (Pierce ECL; Thermo Fisher Scientific) and imaged on ImageQuant LAS400 (Amersham). .. For re-probing the membranes using a different primary antibody, membranes were stripped using the Restore PLUS western blot stripping buffer (Thermo Fischer Scientific) for 15 min at room temperature. .. Control and floxed MEFs were treated with Ad5CMVCre (Ad-Cre), an adenovirus containing Cre recombinase, which was purchased from the Gene Transfer Vector Core at the University of Iowa.

    Stripping:

    Article Title: Proximity Labeling of NIMA Kinase Complex Components in C. elegans
    Article Snippet: .. The resulting blot was imaged, and the membrane was then washed with 1× TBS buffer for 30 seconds and was stripped using Restore PLUS Western Blot Stripping Buffer (Thermo Fisher Scientific, Cat# 46430) for 30 minutes at 37°C with shaking. ..

    Article Title: Supporting Information for Presynaptic neurons self-tune by inversely coupling neurotransmitter release with the abundance of CaV2 voltage-gated Ca2+ channels
    Article Snippet: The PVDF membrane was probed with primary mouse monoclonal anti-ubiquitin antibody (Santa Cruz Biotechnology, sc-8017; WB 1:1,000) and secondary HRP-linked anti-mouse IgG (Cell Signaling Technology, cat# 7076S; WB 1:10,000). .. The PVDF membrane was then stripped with Restore PLUS Western Blot Stripping Buffer (ThermoFisher Scientific, cat# 46430) for 15 minutes. .. The membrane was then probed with primary rabbit monoclonal anti-GFP antibody (Cell Signaling Technology, cat# 2956S WB 1:1,000) and HRP-linked anti-rabbit IgG (Cell Signaling Technology, cat# 7074S WB 1:10,000).

    Article Title: IMPDH inhibition induces DNA replication stress and ATR sensitivity in Merkel cell carcinoma
    Article Snippet: .. For blots that were reblotted, blots were washed with TBST once and then stripped by incubation with Restore PLUS western blot stripping buffer (Thermo Scientific) for 10 min. Blots were then washed three times with TBST and blocked with 5% milk in TBST for 1 h at room temperature. ..

    Article Title: Phenotypic screens for SIRPA expression reveal RAB21 as a general regulator of macrophage surface identity.
    Article Snippet: Flow cytometry-based detection of total CD47 and CD47pyroGlu expression in cells treated with the QPCTL inhibitor SEN177 HAP1, Ramos, THP-1, and U-937 cells were seeded in 96-well plates and treated with a 9-point serial dilution of SEN177 (SigmaAldrich, #SML1615) from 50 μM to 7.6 nM for 72 h. The final volume per well was 100 μL, with 8,000 cells for HAP1, 10,000 for Ramos, 15,000 for U-937, and 30,000 for THP-1. .. After imaging, the IP membrane was stripped with Restore PLUS Western Blot Stripping Buffer (Thermo Scientific, #46430) and blocked, followed by probing with anti-Sirpa antibody, secondary antibody incubation, imaging, and processing as indicated in the ‘‘Western blot detection of total Sirpa levels in RAW264.7 lines’’ section. .. Flow cytometry-based detection of total CD47 and CD47pyroGlu expression in cells treated with the QPCTL inhibitor SEN177 HAP1, Ramos, THP-1, and U-937 cells were seeded in 96-well plates and treated with a 9-point serial dilution of SEN177 (SigmaAldrich, #SML1615) from 50 μM to 7.6 nM for 72 h. The final volume per well was 100 μL, with 8,000 cells for HAP1, 10,000 for Ramos, 15,000 for U-937, and 30,000 for THP-1.

    Article Title: Bruton tyrosine kinase (Btk) in neutrophils is indispensable for initiating and maintaining skin inflammation in a model of pemphigoid diseases.
    Article Snippet: Afterwards, membranes were incubated with rabbit anti-Btk (D3H5; Cell Signaling Technology, Danvers, MA, USA; RRID: AB_10950506) over night and subsequently with horseradish peroxidase-labelled polyclonal goat anti-rabbit (Agilent, Santa Clara, CA, USA; RRID: AB_2617138) for 60 min. Membranes were developed using Clarity Western ECL substrate (BioRad, Feldkirchen, Germany). .. Afterwards, membranes were stripped using Restore Plus Western blot stripping buffer (Thermo Fisher Scientific) according to the manufacturer's instructions, blocked with 5% BSA in TBS-T for 1 h and reprobed with rabbit anti-β-actin (13E5; Cell Signalling Technology; RRID: AB_2223172) and subsequently with HRP-labelled polyclonal goat anti-rabbit for 1 h before developed with ECL substrate. ..

    Article Title: TUG protein acts through a disordered region to organize the early secretory pathway.
    Article Snippet: Control and floxed MEFs were treated withAd5CMVCre (Ad-Cre), an adenovirus containingCre recombinase, which was purchased from the Gene Transfer Vector Core at the University of Iowa. .. For re-probing themembranes using adifferent primaryantibody, membranes were stripped using the Restore PLUS western blot stripping buffer (Thermo Fischer Scientific) for 15min at room temperature. ..

    Article Title: TUG protein acts through a disordered region to organize the early secretory pathway
    Article Snippet: Proteins were detected using chemiluminescence (Pierce ECL; Thermo Fisher Scientific) and imaged on ImageQuant LAS400 (Amersham). .. For re-probing the membranes using a different primary antibody, membranes were stripped using the Restore PLUS western blot stripping buffer (Thermo Fischer Scientific) for 15 min at room temperature. .. Control and floxed MEFs were treated with Ad5CMVCre (Ad-Cre), an adenovirus containing Cre recombinase, which was purchased from the Gene Transfer Vector Core at the University of Iowa.

    Incubation:

    Article Title: IMPDH inhibition induces DNA replication stress and ATR sensitivity in Merkel cell carcinoma
    Article Snippet: .. For blots that were reblotted, blots were washed with TBST once and then stripped by incubation with Restore PLUS western blot stripping buffer (Thermo Scientific) for 10 min. Blots were then washed three times with TBST and blocked with 5% milk in TBST for 1 h at room temperature. ..

    Article Title: Phenotypic screens for SIRPA expression reveal RAB21 as a general regulator of macrophage surface identity.
    Article Snippet: Flow cytometry-based detection of total CD47 and CD47pyroGlu expression in cells treated with the QPCTL inhibitor SEN177 HAP1, Ramos, THP-1, and U-937 cells were seeded in 96-well plates and treated with a 9-point serial dilution of SEN177 (SigmaAldrich, #SML1615) from 50 μM to 7.6 nM for 72 h. The final volume per well was 100 μL, with 8,000 cells for HAP1, 10,000 for Ramos, 15,000 for U-937, and 30,000 for THP-1. .. After imaging, the IP membrane was stripped with Restore PLUS Western Blot Stripping Buffer (Thermo Scientific, #46430) and blocked, followed by probing with anti-Sirpa antibody, secondary antibody incubation, imaging, and processing as indicated in the ‘‘Western blot detection of total Sirpa levels in RAW264.7 lines’’ section. .. Flow cytometry-based detection of total CD47 and CD47pyroGlu expression in cells treated with the QPCTL inhibitor SEN177 HAP1, Ramos, THP-1, and U-937 cells were seeded in 96-well plates and treated with a 9-point serial dilution of SEN177 (SigmaAldrich, #SML1615) from 50 μM to 7.6 nM for 72 h. The final volume per well was 100 μL, with 8,000 cells for HAP1, 10,000 for Ramos, 15,000 for U-937, and 30,000 for THP-1.

    Imaging:

    Article Title: Phenotypic screens for SIRPA expression reveal RAB21 as a general regulator of macrophage surface identity.
    Article Snippet: Flow cytometry-based detection of total CD47 and CD47pyroGlu expression in cells treated with the QPCTL inhibitor SEN177 HAP1, Ramos, THP-1, and U-937 cells were seeded in 96-well plates and treated with a 9-point serial dilution of SEN177 (SigmaAldrich, #SML1615) from 50 μM to 7.6 nM for 72 h. The final volume per well was 100 μL, with 8,000 cells for HAP1, 10,000 for Ramos, 15,000 for U-937, and 30,000 for THP-1. .. After imaging, the IP membrane was stripped with Restore PLUS Western Blot Stripping Buffer (Thermo Scientific, #46430) and blocked, followed by probing with anti-Sirpa antibody, secondary antibody incubation, imaging, and processing as indicated in the ‘‘Western blot detection of total Sirpa levels in RAW264.7 lines’’ section. .. Flow cytometry-based detection of total CD47 and CD47pyroGlu expression in cells treated with the QPCTL inhibitor SEN177 HAP1, Ramos, THP-1, and U-937 cells were seeded in 96-well plates and treated with a 9-point serial dilution of SEN177 (SigmaAldrich, #SML1615) from 50 μM to 7.6 nM for 72 h. The final volume per well was 100 μL, with 8,000 cells for HAP1, 10,000 for Ramos, 15,000 for U-937, and 30,000 for THP-1.

    other:

    Article Title: The role of gene duplication and paralog specialisation in the evolution of the mammalian PRPS complex.
    Article Snippet: Secondary Antibodies used were: Anti mouse (Jackson ImmunoResearch #115-035- 003), Anti rabbit (Jackson ImmunoResearch #111-035-003).



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