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tbs t  (Rockland Immunochemicals)


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    Structured Review

    Rockland Immunochemicals tbs t
    Tbs T, supplied by Rockland Immunochemicals, used in various techniques. Bioz Stars score: 95/100, based on 155 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/tris+buffer/1X+TBS+pH+7%2E8/pmc08268745-172-37-23
    Average 95 stars, based on 155 article reviews
    tbs t - by Bioz Stars, 2026-11
    95/100 stars

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    Related Articles

    Incubation:

    Article Title: Impact of Melatonin on RAW264.7 Macrophages during Mechanical Strain
    Article Snippet: ACTIN (E1C602-2, EnoGene, New York, NY, USA) and PTGS2 (PA5-16817, Thermo Fisher Scientific, Waltham, MA, USA) were used as primary antibodies. .. These were each incubated overnight at 4 °C and after washing three times in TBS-T, the membrane was incubated in the secondary antibody (611-1302, Rockland Immunochemicals, Gilbertsville, PA, USA) for 1 h at room temperature. .. After washing in TBS-T, Luminata Crescendo Western HRP Substrate (WBLUR0100, Sigma Aldrich, St. Louis, MO, USA) was added and the signal was digitized using the VWR Genoplex documentation system (VWR international, Radnor, PA, USA).

    Article Title: Large-Scale Functionalized Metasurface-Based SARS-CoV-2 Detection and Quantification
    Article Snippet: In brief, 100 ng of spike protein in 30 μL was mixed with 10 μL of 4× loading buffer (NuPAGE LDS), heated at 95 °C for 5 min, loaded in 4–12% SDS-polyacrylamide electrophoresis gradient gel (Thermo Fisher-Invitrogen, Waltham, MA, USA), and run at 80 V for 2 h. We then electroblotted the gels onto a nitrocellulose membrane (0.2 μm pore size, Schleicher & Schuell, Keene, NH, USA). .. The membrane was blocked with 5% nonfat dry milk in tris-buffered saline containing 0.01% Tween-20 (TBS-T, pH 7.6) for 30 min and then incubated with the anti-rabbit SPK monoclonal antibody overnight at 4 °C on a rocking platform for 24 h. The following day, the membrane was washed with TBS-T, incubated with the 1:10 000 dilution of a peroxidase conjugated goat anti-rabbit IgG secondary antibody (Rockland Immunochemicals, Gilbersville, PA, USA), and allowed to rock for 2 h at room temperature. .. The blots were washed three times in PBS-T, developed using Pierce ECL Western blotting substrate (Thermo Fisher Scientific, Waltham, MA, USA), and imaged with the IVIS Lumina III in vivo imaging system.

    Article Title: Maternal Undernutrition Induces Cell Signalling and Metabolic Dysfunction in Undifferentiated Mouse Embryonic Stem Cells
    Article Snippet: .. Membranes were washed with TBS-T and probed with primary antibodies (Supplementary Table ) overnight at 4 °C, washing and incubation with secondary antibody conjugated to IRDyeTM 800CW (Rockland Inc. Molecular Probes) near-infrared (IR) fluorochrome for 1 h at room temperature in the dark. .. Following further washing, blots were scanned using the LI-COR Odyssey IR imaging system (LI-COR Biosciences).

    Article Title: Anti‑inflammatory effects of Nypa fruticans Wurmb via NF‑κB and MAPK signaling pathways in macrophages
    Article Snippet: The anti-COX-2 polyclonal antibody (ab15919) and anti-NF-κB p65 polyclonal antibody (ab16502) were purchased from Abcam. .. The membrane was then washed thrice with TBS-T for 15 min. After washing, horse radish peroxidase (HRP)-labeled secondary antibodies, including anti-mouse IgG-HRP monoclonal antibody (18-8817-33, Rockland) and anti-rabbit IgG-HRP monoclonal antibody (18-8816-33) were incubated (1:10,000) for 1 h at room temperature. .. Protein bands were detected using an enhanced chemiluminescence (ECL) substrate solution (Bio-Rad) and visualized using the ChemiDoc imaging system (Bio-Rad).

    Article Title: Simvastatin Abrogates TGF-β Induced Stimulation of Normal Human Dermal Fibroblast Collagen Gene Expression in Culture
    Article Snippet: For Western blot analysis of collagen type I production under basal conditions and under TGF-β1 +/- Simvastatin treatment, the media of the cell cultures were removed and equal aliquots were boiled in an SDS buffer containing 1% β-mercaptoethanol for 5 min, then loaded into 8% or 10% Tris- glycine polyacrylamide gels (Invitrogen) and the proteins separated by electrophoresis as described previously [33]. .. The separated proteins were transferred to a nitrocellulose membrane (Bio-Rad), and incubated in a blocking buffer containing 5% nonfat dry milk in Tris-buffered saline with Tween (TBST) for 1 h. The membrane was incubated with a polyclonal anti-collagen type 1 antibody (Rockland) in a buffer containing 3% nonfat dry milk with TBST at room temperature overnight, washed with TBST and then incubated for 1.5 h with HRP-conjugated antirabbit IgG (Amersham Biosciences). .. After several washes with TBST the immunoreactive bands corresponding to collagen type 1 were visualized by ECL (Amersham Biosciences).

    Article Title: Impact of Leptin on the Expression Profile of Macrophages during Mechanical Strain In Vitro
    Article Snippet: The membranes were incubated in specific primary antibody, i.e., PTGS2 (PA5-16817, Thermo Fisher Scientific, Waltham, MA, USA) and ACTIN (A2066, Sigma-Aldrich, St. Louis, MO, USA), overnight at 4 °C on a roller mixer. .. The membranes were washed three times with TBS-T for 10 min each and incubated with secondary antibody (611-1302, Rockland Immunochemicals, Gilbertsville, PA, USA) for 1 h at room temperature. ..

    Membrane:

    Article Title: Impact of Melatonin on RAW264.7 Macrophages during Mechanical Strain
    Article Snippet: ACTIN (E1C602-2, EnoGene, New York, NY, USA) and PTGS2 (PA5-16817, Thermo Fisher Scientific, Waltham, MA, USA) were used as primary antibodies. .. These were each incubated overnight at 4 °C and after washing three times in TBS-T, the membrane was incubated in the secondary antibody (611-1302, Rockland Immunochemicals, Gilbertsville, PA, USA) for 1 h at room temperature. .. After washing in TBS-T, Luminata Crescendo Western HRP Substrate (WBLUR0100, Sigma Aldrich, St. Louis, MO, USA) was added and the signal was digitized using the VWR Genoplex documentation system (VWR international, Radnor, PA, USA).

    Article Title: Large-Scale Functionalized Metasurface-Based SARS-CoV-2 Detection and Quantification
    Article Snippet: In brief, 100 ng of spike protein in 30 μL was mixed with 10 μL of 4× loading buffer (NuPAGE LDS), heated at 95 °C for 5 min, loaded in 4–12% SDS-polyacrylamide electrophoresis gradient gel (Thermo Fisher-Invitrogen, Waltham, MA, USA), and run at 80 V for 2 h. We then electroblotted the gels onto a nitrocellulose membrane (0.2 μm pore size, Schleicher & Schuell, Keene, NH, USA). .. The membrane was blocked with 5% nonfat dry milk in tris-buffered saline containing 0.01% Tween-20 (TBS-T, pH 7.6) for 30 min and then incubated with the anti-rabbit SPK monoclonal antibody overnight at 4 °C on a rocking platform for 24 h. The following day, the membrane was washed with TBS-T, incubated with the 1:10 000 dilution of a peroxidase conjugated goat anti-rabbit IgG secondary antibody (Rockland Immunochemicals, Gilbersville, PA, USA), and allowed to rock for 2 h at room temperature. .. The blots were washed three times in PBS-T, developed using Pierce ECL Western blotting substrate (Thermo Fisher Scientific, Waltham, MA, USA), and imaged with the IVIS Lumina III in vivo imaging system.

    Article Title: Anti‑inflammatory effects of Nypa fruticans Wurmb via NF‑κB and MAPK signaling pathways in macrophages
    Article Snippet: The anti-COX-2 polyclonal antibody (ab15919) and anti-NF-κB p65 polyclonal antibody (ab16502) were purchased from Abcam. .. The membrane was then washed thrice with TBS-T for 15 min. After washing, horse radish peroxidase (HRP)-labeled secondary antibodies, including anti-mouse IgG-HRP monoclonal antibody (18-8817-33, Rockland) and anti-rabbit IgG-HRP monoclonal antibody (18-8816-33) were incubated (1:10,000) for 1 h at room temperature. .. Protein bands were detected using an enhanced chemiluminescence (ECL) substrate solution (Bio-Rad) and visualized using the ChemiDoc imaging system (Bio-Rad).

    Article Title: Simvastatin Abrogates TGF-β Induced Stimulation of Normal Human Dermal Fibroblast Collagen Gene Expression in Culture
    Article Snippet: For Western blot analysis of collagen type I production under basal conditions and under TGF-β1 +/- Simvastatin treatment, the media of the cell cultures were removed and equal aliquots were boiled in an SDS buffer containing 1% β-mercaptoethanol for 5 min, then loaded into 8% or 10% Tris- glycine polyacrylamide gels (Invitrogen) and the proteins separated by electrophoresis as described previously [33]. .. The separated proteins were transferred to a nitrocellulose membrane (Bio-Rad), and incubated in a blocking buffer containing 5% nonfat dry milk in Tris-buffered saline with Tween (TBST) for 1 h. The membrane was incubated with a polyclonal anti-collagen type 1 antibody (Rockland) in a buffer containing 3% nonfat dry milk with TBST at room temperature overnight, washed with TBST and then incubated for 1.5 h with HRP-conjugated antirabbit IgG (Amersham Biosciences). .. After several washes with TBST the immunoreactive bands corresponding to collagen type 1 were visualized by ECL (Amersham Biosciences).

    Saline:

    Article Title: Large-Scale Functionalized Metasurface-Based SARS-CoV-2 Detection and Quantification
    Article Snippet: In brief, 100 ng of spike protein in 30 μL was mixed with 10 μL of 4× loading buffer (NuPAGE LDS), heated at 95 °C for 5 min, loaded in 4–12% SDS-polyacrylamide electrophoresis gradient gel (Thermo Fisher-Invitrogen, Waltham, MA, USA), and run at 80 V for 2 h. We then electroblotted the gels onto a nitrocellulose membrane (0.2 μm pore size, Schleicher & Schuell, Keene, NH, USA). .. The membrane was blocked with 5% nonfat dry milk in tris-buffered saline containing 0.01% Tween-20 (TBS-T, pH 7.6) for 30 min and then incubated with the anti-rabbit SPK monoclonal antibody overnight at 4 °C on a rocking platform for 24 h. The following day, the membrane was washed with TBS-T, incubated with the 1:10 000 dilution of a peroxidase conjugated goat anti-rabbit IgG secondary antibody (Rockland Immunochemicals, Gilbersville, PA, USA), and allowed to rock for 2 h at room temperature. .. The blots were washed three times in PBS-T, developed using Pierce ECL Western blotting substrate (Thermo Fisher Scientific, Waltham, MA, USA), and imaged with the IVIS Lumina III in vivo imaging system.

    Article Title: Simvastatin Abrogates TGF-β Induced Stimulation of Normal Human Dermal Fibroblast Collagen Gene Expression in Culture
    Article Snippet: For Western blot analysis of collagen type I production under basal conditions and under TGF-β1 +/- Simvastatin treatment, the media of the cell cultures were removed and equal aliquots were boiled in an SDS buffer containing 1% β-mercaptoethanol for 5 min, then loaded into 8% or 10% Tris- glycine polyacrylamide gels (Invitrogen) and the proteins separated by electrophoresis as described previously [33]. .. The separated proteins were transferred to a nitrocellulose membrane (Bio-Rad), and incubated in a blocking buffer containing 5% nonfat dry milk in Tris-buffered saline with Tween (TBST) for 1 h. The membrane was incubated with a polyclonal anti-collagen type 1 antibody (Rockland) in a buffer containing 3% nonfat dry milk with TBST at room temperature overnight, washed with TBST and then incubated for 1.5 h with HRP-conjugated antirabbit IgG (Amersham Biosciences). .. After several washes with TBST the immunoreactive bands corresponding to collagen type 1 were visualized by ECL (Amersham Biosciences).

    Article Title: Differential dysregulation of granule subsets in WASH-deficient neutrophil leukocytes resulting in inflammation
    Article Snippet: .. The membranes were blocked with tris-buffered saline (TBS) containing 5% (wt/vol) blotting-grade nonfat dry milk blocker (Rockland, Limerick, PA) and 0.1% (wt/vol) Tween 20. .. Proteins were detected by probing the membranes with the indicated primary antibodies at appropriate dilutions and using a detection system consisting of horseradish peroxidase–conjugated secondary antibodies (Bio-Rad Laboratories, Hercules, CA) and the chemiluminescence substrates SuperSignal, WestPico, and WestFemto (Thermo Scientific) and then visualized using the c600 Azure Biosystem or by film development.

    Transcranial Magnetic Stimulation:

    Article Title: Anti‑inflammatory effects of Nypa fruticans Wurmb via NF‑κB and MAPK signaling pathways in macrophages
    Article Snippet: The anti-COX-2 polyclonal antibody (ab15919) and anti-NF-κB p65 polyclonal antibody (ab16502) were purchased from Abcam. .. The membrane was then washed thrice with TBS-T for 15 min. After washing, horse radish peroxidase (HRP)-labeled secondary antibodies, including anti-mouse IgG-HRP monoclonal antibody (18-8817-33, Rockland) and anti-rabbit IgG-HRP monoclonal antibody (18-8816-33) were incubated (1:10,000) for 1 h at room temperature. .. Protein bands were detected using an enhanced chemiluminescence (ECL) substrate solution (Bio-Rad) and visualized using the ChemiDoc imaging system (Bio-Rad).

    Article Title: Impact of Leptin on the Expression Profile of Macrophages during Mechanical Strain In Vitro
    Article Snippet: The membranes were incubated in specific primary antibody, i.e., PTGS2 (PA5-16817, Thermo Fisher Scientific, Waltham, MA, USA) and ACTIN (A2066, Sigma-Aldrich, St. Louis, MO, USA), overnight at 4 °C on a roller mixer. .. The membranes were washed three times with TBS-T for 10 min each and incubated with secondary antibody (611-1302, Rockland Immunochemicals, Gilbertsville, PA, USA) for 1 h at room temperature. ..

    Blocking Assay:

    Article Title: Simvastatin Abrogates TGF-β Induced Stimulation of Normal Human Dermal Fibroblast Collagen Gene Expression in Culture
    Article Snippet: For Western blot analysis of collagen type I production under basal conditions and under TGF-β1 +/- Simvastatin treatment, the media of the cell cultures were removed and equal aliquots were boiled in an SDS buffer containing 1% β-mercaptoethanol for 5 min, then loaded into 8% or 10% Tris- glycine polyacrylamide gels (Invitrogen) and the proteins separated by electrophoresis as described previously [33]. .. The separated proteins were transferred to a nitrocellulose membrane (Bio-Rad), and incubated in a blocking buffer containing 5% nonfat dry milk in Tris-buffered saline with Tween (TBST) for 1 h. The membrane was incubated with a polyclonal anti-collagen type 1 antibody (Rockland) in a buffer containing 3% nonfat dry milk with TBST at room temperature overnight, washed with TBST and then incubated for 1.5 h with HRP-conjugated antirabbit IgG (Amersham Biosciences). .. After several washes with TBST the immunoreactive bands corresponding to collagen type 1 were visualized by ECL (Amersham Biosciences).

    Article Title: EXO1-mediated DNA repair by single-strand annealing is essential for BRCA1-deficient cells
    Article Snippet: Proteins were separated by SDS-PAGE on 4-12 % gradient gels (ThermoFisher Scientific) or 4-15% Criterion TGX pre-cast midi protein gel (Bio-Rad, Hercules, CA, USA) and transferred to Amersham Protran premium 0.45 μm nitrocellulose membrane (GE Healthcare Life Sciences, Chicago, IL, USA). .. Membranes were blocked with 5% skimmed milk (Santa Cruz Biotechnology, Dallas, TX, USA) in 1x TBS or Blocking buffer for fluorescent WB (Rockland, Pottstown, PA, USA), and stained with primary and secondary antibodies. .. After secondary antibody-staining, the membranes were imaged on an Odyssey CLx scanner (LI-COR BioSciences, Milton, UK), followed by image analysis using ImageStudio (LI-COR BioSciences).

    Western Blot:

    Article Title: EXO1-mediated DNA repair by single-strand annealing is essential for BRCA1-deficient cells
    Article Snippet: Proteins were separated by SDS-PAGE on 4-12 % gradient gels (ThermoFisher Scientific) or 4-15% Criterion TGX pre-cast midi protein gel (Bio-Rad, Hercules, CA, USA) and transferred to Amersham Protran premium 0.45 μm nitrocellulose membrane (GE Healthcare Life Sciences, Chicago, IL, USA). .. Membranes were blocked with 5% skimmed milk (Santa Cruz Biotechnology, Dallas, TX, USA) in 1x TBS or Blocking buffer for fluorescent WB (Rockland, Pottstown, PA, USA), and stained with primary and secondary antibodies. .. After secondary antibody-staining, the membranes were imaged on an Odyssey CLx scanner (LI-COR BioSciences, Milton, UK), followed by image analysis using ImageStudio (LI-COR BioSciences).

    Staining:

    Article Title: EXO1-mediated DNA repair by single-strand annealing is essential for BRCA1-deficient cells
    Article Snippet: Proteins were separated by SDS-PAGE on 4-12 % gradient gels (ThermoFisher Scientific) or 4-15% Criterion TGX pre-cast midi protein gel (Bio-Rad, Hercules, CA, USA) and transferred to Amersham Protran premium 0.45 μm nitrocellulose membrane (GE Healthcare Life Sciences, Chicago, IL, USA). .. Membranes were blocked with 5% skimmed milk (Santa Cruz Biotechnology, Dallas, TX, USA) in 1x TBS or Blocking buffer for fluorescent WB (Rockland, Pottstown, PA, USA), and stained with primary and secondary antibodies. .. After secondary antibody-staining, the membranes were imaged on an Odyssey CLx scanner (LI-COR BioSciences, Milton, UK), followed by image analysis using ImageStudio (LI-COR BioSciences).



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