pbs thermo fisher scientific (Thermo Fisher)

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Thermo Fisher pbs thermo fisher scientific
Pbs Thermo Fisher Scientific, 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/microarray+hybridization+buffer+ii/PBS/pm30096312-291-71-72
Average 99 stars, based on 1 article reviews

pbs thermo fisher scientific - by Bioz Stars, 2026-10

99/100 stars

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Article Title: Derivatives of dolaproine-dolaisoleuine peptides
Article Snippet: After 72 h of acclimatization, the mice are implanted with SW780 human bladder cancer cells (2×106 cells/mouse), suspended in 50% complete cultrex (Trevigen, Inc.) mixed with PBS (Gibco), and the tumor growth rate is monitored.

Incubation:

Article Title: Biomineralized outer membrane vesicles for synergistic immuno-photodynamic therapy of oral squamous cell carcinoma
Article Snippet: .. First, OMVs containing 1 mg of total protein were dispersed in 1 mL of PBS (Gibco) and incubated overnight in a constant-temperature shaking incubator (200 rpm) at 37 °C to reach equilibrium. ..

Article Title: Compound design of a patient-derived 3D cell culture system modelling early peritoneal endometriosis
Article Snippet: Cells were permeabilised with 0.25% (v/v) Triton X-100 (Thermo Fisher Scientific, 85111) in PBS for 10 min at RT and blocked with 2% (w/v) bovine serum albumin (BSA; Sigma-Aldrich, A3803) for 1 h at RT. .. Cells were incubated with primary antibodies overnight at 4°C , followed by three 15 min PBS washes and incubation with secondary antibodies AlexaFluor 488 goat-anti-mouse IgG1 (Invitrogen, A21121) and AlexaFluor 568 goat-anti-rabbit (Invitrogen, A11011) at 1:1000 dilution, and DAPI (Sigma-Aldrich, D9542) in a 1:500 dilution, for 1 h at RT. .. The slides were mounted using Fluoromount (Invitrogen, 00-4958-02).

Article Title: Immunomodulatory topographies regulate myofibroblast differentiation and influence fibrous encapsulation of glaucoma drainage devices
Article Snippet: Next, the cells were permeabilized with 0.5 % Triton X-100 (Merck) dissolved in PBS for 10 min and blocked with 3 % (w/v) bovine serum albumin (Merck) in PBS for 30 min and then with 5 % (v/v) goat serum (Fisher Scientific) dissolved in PBS for 30 min. Next, cells were incubated with a primary antibody using mouse monoclonal anti α-smooth muscle actin diluted in PBS (1:600; Sigma: A5228) overnight at 4 °C. .. The next day, the cells were washed 3 times with PBS and then incubated with a secondary antibody goat anti-mouse Alexa Flour 488 diluted in PBS (1:500; Molecular probes: A21121) and incubated in the dark for 1 h at room temperature. .. For the α-SMA screen, cells were washed three times with PBS and stained with phalloidin-TRITC diluted in PBS (1:200, ThermoFisher) for 45 min and washed 3 times again with PBS and stained with 4′,6-Diamidino-2-Phenylindole (DAPI) (Sigma Aldrich; 1:500) for 15 min. For the macrophage screen, the cell membrane was stained using CellMask orange (1:1000; ThermoFisher) for 10 min at room temperature.

Incubator:

Staining:

Article Title: Immunomodulatory topographies regulate myofibroblast differentiation and influence fibrous encapsulation of glaucoma drainage devices
Article Snippet: The next day, the cells were washed 3 times with PBS and then incubated with a secondary antibody goat anti-mouse Alexa Flour 488 diluted in PBS (1:500; Molecular probes: A21121) and incubated in the dark for 1 h at room temperature. .. For the α-SMA screen, cells were washed three times with PBS and stained with phalloidin-TRITC diluted in PBS (1:200, ThermoFisher) for 45 min and washed 3 times again with PBS and stained with 4′,6-Diamidino-2-Phenylindole (DAPI) (Sigma Aldrich; 1:500) for 15 min. For the macrophage screen, the cell membrane was stained using CellMask orange (1:1000; ThermoFisher) for 10 min at room temperature. .. Afterward, cells were washed with PBS 3 times and stained with DAPI (Sigma Aldrich; 1:500) for 15 min. After staining, all the surfaces were washed three times with PBS after which they were mounted onto a glass slide using Mowiol (Sigma).

Membrane:

Article Title: Immunomodulatory topographies regulate myofibroblast differentiation and influence fibrous encapsulation of glaucoma drainage devices
Article Snippet: The next day, the cells were washed 3 times with PBS and then incubated with a secondary antibody goat anti-mouse Alexa Flour 488 diluted in PBS (1:500; Molecular probes: A21121) and incubated in the dark for 1 h at room temperature. .. For the α-SMA screen, cells were washed three times with PBS and stained with phalloidin-TRITC diluted in PBS (1:200, ThermoFisher) for 45 min and washed 3 times again with PBS and stained with 4′,6-Diamidino-2-Phenylindole (DAPI) (Sigma Aldrich; 1:500) for 15 min. For the macrophage screen, the cell membrane was stained using CellMask orange (1:1000; ThermoFisher) for 10 min at room temperature. .. Afterward, cells were washed with PBS 3 times and stained with DAPI (Sigma Aldrich; 1:500) for 15 min. After staining, all the surfaces were washed three times with PBS after which they were mounted onto a glass slide using Mowiol (Sigma).

Sequencing:

Article Title: Haplotype-resolved genome assemblies of BJ and IMR-90 human fibroblast cell lines reveal extensive structural variation and enable reanalysis of historical sequencing data
Article Snippet: Both cell lines were authenticated by STR profiling at ATCC ( https://www.atcc.org/ , last accessed 27 February 2026). .. Cells for sequencing were harvested with 0.25% Trypsin–ethylenediaminetetraacetic acid (EDTA) (Thermo Fisher, Cat. No. 25200072), washed with 1× PBS (pH 7.4; Thermo Fisher, Cat. No. 10010023), counted on a Countess II FL Automated Cell Counter (Thermo Fisher, Cat. No. AMQAF1000), and used as input for NEB Monarch HMW genomic DNA (gDNA) isolation, Hi-C crosslinking, RNeasy Plus Mini isolation, or frozen as dry pellets and stored at −80°C for use in Oxford Nanopore Technologies (ONT) Ultra-Long (UL) library preparations. .. Estimated cumulative population doubling level (PDL) calculations were performed using PDL = 3.32 (logXe-logXb) + S where log is the base 10 logarithm, Xb is the cell number at the beginning of the incubation period, Xe is the cell number at the end of the incubation period, and S is the starting PDL (ref ATCC Animal Cell Culture Guide ACCG-042024-v08, p6).