congo red staining solution (Thermo Fisher)

Thermo Fisher is a verified supplier

Thermo Fisher manufactures this product

About

News

Press Release

Team

Advisors

Partners

Contact

Bioz Stars

Bioz vStars

Buy from Supplier

Structured Review

Thermo Fisher congo red staining solution
Congo Red Staining Solution, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/congo-red+solution/pm40500460-36-1-17
Average 90 stars, based on 1 article reviews

congo red staining solution - by Bioz Stars, 2026-10

90/100 stars

Images

Sterility:

Article Title: Biofilm Formation in Arcobacter butzleri and Arcobacter cryaerophilus: Phenotypic and Genotypic Characterization of Food and Environmental Isolates
Article Snippet: .. CRA was composed of 37 g/L Brain Heart Infusion broth, 10 g/L agar, and 0.1 g/L sterile Congo red solution (CAS: 573-58-0; Acros Organics, Geel, Belgium) [22,23]. ..

Article Title: Hydrophilic inflatable penile prosthesis surface coatings readily rebind antibiotics and maintain antimicrobial efficacy ex vivo.
Article Snippet: .. A Congo Red staining solution at 25 g/L was made using sterile water according to manufacturer recommendations (ThermoFischer ScientificTM, Waltham, MA). .. PP were submerged in Congo Red solution for 5 min, after which the material was rinsed in sterile NS to remove any loosely adherent dye, covered in aluminum foil to protect from light which could cause degradation of the Congo Red dye, dried in a laminar flow hood for two hours, and evaluated at low and high magnification microscopically, using a Nikon® Eclipse E600 microscope (Tokyo, Japan) [10].

Article Title: Biofilm Formation in Arcobacter butzleri and Arcobacter cryaerophilus : Phenotypic and Genotypic Characterization of Food and Environmental Isolates
Article Snippet: .. CRA was composed of 37 g/L Brain Heart Infusion broth, 10 g/L agar, and 0.1 g/L sterile Congo red solution (CAS: 573-58-0; Acros Organics, Geel, Belgium) [ , ]. ..

Staining:

Concentration Assay:

Article Title: Effect of ultrasonic-assisted H 2 O 2 /ascorbic acid modification on Platycodon grandiflorum polysaccharide: structural characterization and in vitro functional activities.
Article Snippet: .. Congo red solution (80 μmol/L, 2 mL) was mixed with polysaccharide solution (2 mg/mL, 2 mL), followed by addition of NaOH solution (1 mol/L) to achieve a final NaOH concentration of 0–0.5 mol/ L. After reacting at room temperature for 5 min, the maximum absorption wavelength (λ_max) was measured using a microplate reader (Multiskan, Thermo Fisher Scientific, MA, USA). .. Thermal stability was evaluated using a thermogravimetric analyzer (NETZSCH TG209F3, Shanghai, China).

Incubation:

Article Title: Divergent CPEB prion-like domains reveal different assembly mechanisms for a generic amyloid-like fold
Article Snippet: .. After the incubation time, the protein solutions were mixed with a 30 μ M Congo Red solution (in 5 mM sodium phosphate buffer+300 mM NaCl, pH 7.5) and incubated at room temperature for 30 min. Congo Red binding was calculated by measuring bathochromic and hyperchromic shifts in the samples, using a UV-visible spectrophotometer (Nanodrop, Thermo Scientific), and applying the following equation Congo Red μ /mol/l) = A 540 /25,295 – A 480 /46,306 ( ). .. Congo Red bound to amyloid aggregates exhibited typical applegreen birefringence, as monitored under polarized light Leica DMI6000B inverted optical microscope (Leica Microsystems).

Binding Assay:

Spectrophotometry:

other:

Article Title: Influence of electrostatic interactions on the fibrillation process of human serum albumin.
Article Snippet: The fibrillation propensity of the multidomain protein human serum albumin (HSA) has been analyzed under physiological and acidic conditions at room and elevated temperatures with varying ionic strengths by different spectroscopic techniques.. The kinetics of fibril formation under the different solution conditions and the structures of resulting fibrillar aggregates were also determined.. In this way, we have observed that fibril formation is largely affected by electrostatic shielding: at physiological pH, fibrillation is progressively more efficient and faster in the presence of up to 50 mM NaCl; meanwhile, at larger salt concentrations, excessive shielding and further enhancement of the solution hydrophobicity might involve a change in the energy landscape of the aggregation process, which makes the fibrillation process difficult.

Review