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cas  (Thermo Fisher)


Bioz Verified Symbol Thermo Fisher is a verified supplier
Bioz Manufacturer Symbol Thermo Fisher manufactures this product  
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  • 94

    Structured Review

    Thermo Fisher cas
    Cas, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/sucrose/Sucrose%2C+Molecular+Biology+Grade/pmc13091047-17-9-5
    Average 94 stars, based on 1 article reviews
    cas - by Bioz Stars, 2026-09
    94/100 stars

    Images

    Related Articles

    Immunofluorescence:

    Article Title: NuMA1 controls myonuclear motility in striated skeletal muscle through AMPK activity and is impaired in Duchenne muscular dystrophy.
    Article Snippet: .. Primary myoblasts were put in differentiation media for 3 days before fixation in 4% PFA (Thermoscientific 043368.9M)/ 4% sucrose (Acros organics 177140010) in PBS for 20 min at 37°C and immunofluorescence protocol followed. .. - On primary cells Cells were fixed in 4% paraformaldehyde (Thermoscientific 043368.9M) – 4% sucrose (Acros organics 177140010) – 0,1% TritonX-100 in PBS for 20 min at 37°C followed by washes with PBS and membranes permeabilization with 0.5% Triton-X100 in PBS for 5 min at Room Temperature (RT).

    Imaging:

    Article Title: Kinemomics: spatiotemporal morphodynamic mapping of ventricular kinematic subpopulations in organotypic fetal heart slices
    Article Snippet: .. After live imaging, heart slice sections were fixed with 4% PFA overnight at 4°C, washed with 1x phosphate-buffered saline (PBS; Gibco, 20012-027) twice for at least 1 hr, placed in 15% sucrose (Thermo Scientific, A15583.36) in PBS at 4°C until sinks, then transferred into 30% sucrose in PBS until sinks. ..

    Saline:

    Article Title: Kinemomics: spatiotemporal morphodynamic mapping of ventricular kinematic subpopulations in organotypic fetal heart slices
    Article Snippet: .. After live imaging, heart slice sections were fixed with 4% PFA overnight at 4°C, washed with 1x phosphate-buffered saline (PBS; Gibco, 20012-027) twice for at least 1 hr, placed in 15% sucrose (Thermo Scientific, A15583.36) in PBS at 4°C until sinks, then transferred into 30% sucrose in PBS until sinks. ..

    Incubation:

    Article Title: Nicotinamide-Loaded Peptoid Nanotubes for Energy Regeneration in Acute Brain Injury.
    Article Snippet: .. The inhibitors used were chlorpromazine hydrochloride (Sigma), cytochalasin D (Sigma), amiloride hydrochloride hydrate (Sigma), sucrose (Thermo Fisher Scientific), and genistein (Sigma).72−75 After treatment, cells were incubated with LysoTracker (75 nM, Invitrogen) for 1 h and fixed with 10% formalin phosphate buffer (Thermo Fisher Scientific) for 10 min. .. Subsequently, cells were stained with Tomato Lectin (1 μg/mL, 1 h) and ToPro-3 (0.1 μg/mL, 15 min; Thermo Fisher Scientific) in PBS at room temperature.

    Sterility:

    Article Title: Priming of defence signalling in grapevine cells depends on actin filaments.
    Article Snippet: Cell cultivation and priming by aluminium Suspension cultures of Vitis rupestris were grown in a modified Murashige-Skoog liquid at weekly subcultivation as described previously (Maisch and Nick 2007). .. For 1 3 priming by aluminium (Fig. 1A), cells were collected by sterile filtration through a bottle-top filter (Nalgene) and resuspended in 3% sucrose, acidified to pH 4.5 using 1 M HCl and supplemented with 3 mM CaCl2 and 200 μM AlCl3 (Sigma-Aldrich, Deisenhofen, Germany). .. The cells were then returned to the shaker for another 2 h before elicitation with harpin 9 μg·mL− 1 (ProAct, 1% w/v harpin protein, Plant Health Cure, Ojsterwijk, Netherlands).

    Filtration:

    Article Title: Priming of defence signalling in grapevine cells depends on actin filaments.
    Article Snippet: Cell cultivation and priming by aluminium Suspension cultures of Vitis rupestris were grown in a modified Murashige-Skoog liquid at weekly subcultivation as described previously (Maisch and Nick 2007). .. For 1 3 priming by aluminium (Fig. 1A), cells were collected by sterile filtration through a bottle-top filter (Nalgene) and resuspended in 3% sucrose, acidified to pH 4.5 using 1 M HCl and supplemented with 3 mM CaCl2 and 200 μM AlCl3 (Sigma-Aldrich, Deisenhofen, Germany). .. The cells were then returned to the shaker for another 2 h before elicitation with harpin 9 μg·mL− 1 (ProAct, 1% w/v harpin protein, Plant Health Cure, Ojsterwijk, Netherlands).



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