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ice cold phosphate buffer saline solution pbs  (Thermo Fisher)


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    Structured Review

    Thermo Fisher ice cold phosphate buffer saline solution pbs
    Ice Cold Phosphate Buffer Saline Solution Pbs, supplied by Thermo Fisher, 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/product/ice+cold+phosphate+buffer+solution+pbs/Phosphate/pmc12901124-71-8-17
    Average 99 stars, based on 1 article reviews
    ice cold phosphate buffer saline solution pbs - by Bioz Stars, 2026-10
    99/100 stars

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    Radio Immunoprecipitation:

    Article Title: Oncometabolite D-2-Hydroxyglurate Directly Induces Epithelial-Mesenchymal Transition and is Associated with Distant Metastasis in Colorectal Cancer
    Article Snippet: Cycle sequencing was carried out using the BigDye Terminator v3.1 Cycle Sequencing kit (Thermo Fisher Scientific, MA). .. After washing the cells in ice-cold phosphate buffer solution (PBS), cells were pelleted and total protein extracts were made by lysing in radio-immunoprecipitation assay (RIPA) buffer (Thermo Fisher Scientific, MA). .. Cell lysates were measured for their protein concentrations using the Bradford method (BioRad, CA), after which they were separated by sodium dodecyl sulfate–polyacrylamide gel electrophoresis, then transferred to polyvinylidene difluoride membranes using iBlot (Life Technologies, CA).

    Lysis:

    Article Title: Acetylcholine muscarinic M2 receptor maintains human Schwann-like adipose-derived phenotype in the absence of differentiating medium.
    Article Snippet: .. For protein analysis, cells were rinsed with ice-cold phosphate buffer solution (PBS) and scraped in RIPA lysis buffer (Sigma-Aldrich, UK) containing a cocktail of protease and phosphatase inhibitors (Thermo Fisher Scientific, Loughborough, UK) and the whole cell lysates were used for western blot analysis (see Protein Extraction and Western blot section). .. For qPCR analysis, cells were scraped with RNA protect cell reagent (Qiagen, Manchester, UK) and then processed as described in ‘Quantitative real-time polymerase chain reaction (qRT-PCR)’.

    Article Title: Predominant enhancement of apoptosis induced by methyl jasmonate in bladder cancer cells
    Article Snippet: Methyl jasmonate (MJ) has recently attracted attention as a promising antitumoral compound because of its highly specific proapoptotic properties in a wide range of malignancies.. However, the high doses required to achieve a therapeutic benefit have limited its clinical development.. Here, we hypothesize that the family of inhibitor of apoptosis proteins (IAPs) may inhibit MJ-mediated apoptosis in cancer cells.

    Article Title: Bergamot essential oil nanoemulsions: antimicrobial and cytotoxic activity.
    Article Snippet: After evaluating cell cytotoxicity, the total protein content was determinedbyusing theMicroBCAprotein assaykit (ThermoFisher Scientific Inc., US). .. Briefly, the cells were washed with ice-cold phosphate buffer solution (PBS), and incubated for 15 min with 150 μL RIPA lysis buffer (Thermo Scientific, 89900), followed by the addition of 150 mL of Micro BCA working reagent and incubated at 37 °C for 2 h, according to manufacturer’s instructions. ..

    Western Blot:

    Article Title: Acetylcholine muscarinic M2 receptor maintains human Schwann-like adipose-derived phenotype in the absence of differentiating medium.
    Article Snippet: .. For protein analysis, cells were rinsed with ice-cold phosphate buffer solution (PBS) and scraped in RIPA lysis buffer (Sigma-Aldrich, UK) containing a cocktail of protease and phosphatase inhibitors (Thermo Fisher Scientific, Loughborough, UK) and the whole cell lysates were used for western blot analysis (see Protein Extraction and Western blot section). .. For qPCR analysis, cells were scraped with RNA protect cell reagent (Qiagen, Manchester, UK) and then processed as described in ‘Quantitative real-time polymerase chain reaction (qRT-PCR)’.

    Protein Extraction:

    Article Title: Acetylcholine muscarinic M2 receptor maintains human Schwann-like adipose-derived phenotype in the absence of differentiating medium.
    Article Snippet: .. For protein analysis, cells were rinsed with ice-cold phosphate buffer solution (PBS) and scraped in RIPA lysis buffer (Sigma-Aldrich, UK) containing a cocktail of protease and phosphatase inhibitors (Thermo Fisher Scientific, Loughborough, UK) and the whole cell lysates were used for western blot analysis (see Protein Extraction and Western blot section). .. For qPCR analysis, cells were scraped with RNA protect cell reagent (Qiagen, Manchester, UK) and then processed as described in ‘Quantitative real-time polymerase chain reaction (qRT-PCR)’.

    Incubation:

    Article Title: Predominant enhancement of apoptosis induced by methyl jasmonate in bladder cancer cells
    Article Snippet: Methyl jasmonate (MJ) has recently attracted attention as a promising antitumoral compound because of its highly specific proapoptotic properties in a wide range of malignancies.. However, the high doses required to achieve a therapeutic benefit have limited its clinical development.. Here, we hypothesize that the family of inhibitor of apoptosis proteins (IAPs) may inhibit MJ-mediated apoptosis in cancer cells.

    Article Title: Bergamot essential oil nanoemulsions: antimicrobial and cytotoxic activity.
    Article Snippet: After evaluating cell cytotoxicity, the total protein content was determinedbyusing theMicroBCAprotein assaykit (ThermoFisher Scientific Inc., US). .. Briefly, the cells were washed with ice-cold phosphate buffer solution (PBS), and incubated for 15 min with 150 μL RIPA lysis buffer (Thermo Scientific, 89900), followed by the addition of 150 mL of Micro BCA working reagent and incubated at 37 °C for 2 h, according to manufacturer’s instructions. ..

    Isolation:

    Article Title: Repeated Aconitine Treatment Induced the Remodeling of Mitochondrial Function via AMPK–OPA1–ATP5A1 Pathway
    Article Snippet: .. In brief, after cervical dislocation and disinfection, the heart tissues were immediately isolated and placed into the ice-cold phosphate buffer solution (PBS) (Gibco, Thermo Fisher Scientific, Waltham, MA, United States). .. After rinsing 4 times, the ventricular tissues were cut into less than 1 mm 3 tissue block and digested in trypsin (0.0625%, Sigma-Aldrich, St. Louis, MO, United States) for 5 min at room temperature (RT), followed by 5 min collagenase II (1 mg/ml, Solarbio, Beijing, China) enzymolysis at 37°C.



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