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paraformaldehyde solution  (Thermo Fisher)


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    Structured Review

    Thermo Fisher paraformaldehyde solution
    Paraformaldehyde Solution, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/fixative+solution/Paraformaldehyde+fixative+solution/pm42331167-97-6-38
    Average 97 stars, based on 1 article reviews
    paraformaldehyde solution - by Bioz Stars, 2026-10
    97/100 stars

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    Related Articles

    Infection:

    Article Title: Rational Design of a Chimpanzee Adenoviral-Vector Vaccine Against Yellow Fever Through the Modification of Antigen Transmembrane Domains.
    Article Snippet: .. T-RexTM-293 cells (Thermo Fisher Scientific, UK) grown on glass coverslips of 13 mm diameter were infected at a MOI of 10 IU/cell with ChAdOx1 viruses and incubated at 37 ◦C under 5% CO2 for 18 h. After 18 h, the cells were fixed with Image-ITTM Paraformaldehyde 4% Fixative solution (Thermo Scientific, UK) for 10 min at room temperature (RT), followed by permeabilization with a PBS buffer containing 0.1% v/v Triton-X100 in PBS. .. The YFV E proteins were visualized using the Yellow Fever Virus antibody 2D12 (0G5) (Bio-Rad, Watford, UK), and the Golgi apparatus was visualized using the Anti-GM130 antibody [EP892Y] cis-Golgi Marker (Abcam, Cambridge, UK), both at dilutions of 1:100 in a PBS buffer containing 2% v/v FBS (blocking buffer), for 1 h at RT.

    Incubation:

    Article Title: Rational Design of a Chimpanzee Adenoviral-Vector Vaccine Against Yellow Fever Through the Modification of Antigen Transmembrane Domains.
    Article Snippet: .. T-RexTM-293 cells (Thermo Fisher Scientific, UK) grown on glass coverslips of 13 mm diameter were infected at a MOI of 10 IU/cell with ChAdOx1 viruses and incubated at 37 ◦C under 5% CO2 for 18 h. After 18 h, the cells were fixed with Image-ITTM Paraformaldehyde 4% Fixative solution (Thermo Scientific, UK) for 10 min at room temperature (RT), followed by permeabilization with a PBS buffer containing 0.1% v/v Triton-X100 in PBS. .. The YFV E proteins were visualized using the Yellow Fever Virus antibody 2D12 (0G5) (Bio-Rad, Watford, UK), and the Golgi apparatus was visualized using the Anti-GM130 antibody [EP892Y] cis-Golgi Marker (Abcam, Cambridge, UK), both at dilutions of 1:100 in a PBS buffer containing 2% v/v FBS (blocking buffer), for 1 h at RT.

    Article Title: Programmed DNA elimination was present in the last common ancestor of Caenorhabditis nematodes
    Article Snippet: .. Worms were then dissected in 10 μl of 1 mM levamisole on poly-L-lysine-coated slides, freeze-cracked, and fixed in pre-chilled methanol (−30°C) in a fixation jar for 10 min. Each slide was washed twice in PBST (0.05% Tween-20 in 1X PBS buffer), followed by incubation with 40 μl of fixative solution (3.7% formaldehyde, 0.8% methanol in 1X PBS) for 10 min. After a PBST wash, slides were treated with 2X SSCT (2X saline-sodium citrate [SSC] buffer [Thermo Fisher Scientific: 15557–04] and 0.5% Triton X-100). .. They were incubated in denaturation buffer (50% formamide in 1X SSCT) at 60°C for 30 min, then overlaid with 10 μl of probe mixture (10% dextran sulfate, 2X SSC, 50% formamide, 1 μM of DNA probe [Ca_SR2: 5’-Alexa488-GTGGACAAAAATCGACAAAACAAAGACC-3’ (Eurofins), Ca_SR8: 5’-CY3-CAGTTTTGACGTCATCAGTTCAA-3’ (Eurofins), Telomere: 5’-CY3-TTAGGCTTAGGCTTAGGCTTAGGC-CY3-3’, (Integrated DNA Technologies)], 1 mg/ml of RNase A and 0.1% Tween-20).

    Saline:

    Article Title: Programmed DNA elimination was present in the last common ancestor of Caenorhabditis nematodes
    Article Snippet: .. Worms were then dissected in 10 μl of 1 mM levamisole on poly-L-lysine-coated slides, freeze-cracked, and fixed in pre-chilled methanol (−30°C) in a fixation jar for 10 min. Each slide was washed twice in PBST (0.05% Tween-20 in 1X PBS buffer), followed by incubation with 40 μl of fixative solution (3.7% formaldehyde, 0.8% methanol in 1X PBS) for 10 min. After a PBST wash, slides were treated with 2X SSCT (2X saline-sodium citrate [SSC] buffer [Thermo Fisher Scientific: 15557–04] and 0.5% Triton X-100). .. They were incubated in denaturation buffer (50% formamide in 1X SSCT) at 60°C for 30 min, then overlaid with 10 μl of probe mixture (10% dextran sulfate, 2X SSC, 50% formamide, 1 μM of DNA probe [Ca_SR2: 5’-Alexa488-GTGGACAAAAATCGACAAAACAAAGACC-3’ (Eurofins), Ca_SR8: 5’-CY3-CAGTTTTGACGTCATCAGTTCAA-3’ (Eurofins), Telomere: 5’-CY3-TTAGGCTTAGGCTTAGGCTTAGGC-CY3-3’, (Integrated DNA Technologies)], 1 mg/ml of RNase A and 0.1% Tween-20).

    Staining:

    Article Title: Surface‐Capped Protein Nanoparticles for Nonviral Gene Delivery
    Article Snippet: .. After fixation, the fixative solution was discarded, and the cells were washed gently with PBS 3 times, followed by permeabilization with 0.25% Triton‐X100 (in PBS) for 10 min. After the permeabilization solution was discarded, and the cells were washed 3 times with PBS, Alexa Fluor 488 Phalloidin (1:400, Invitrogen) solution was added to each well to stain the cytoskeleton. .. To visualize the cell nuclei, scaffolds were stained with DAPI staining solution (1:1000, Abcam) for 10 min at RT.



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