natural biomacromolecules such as structural proteins and polysaccharides composed of the basic building blocks of life: amino acids and carbohydrates. Understand their molecular structure, self-assembly and interaction in solvents such as ionic liquids (ILS) is very important to release new material flora, revolutionizing the way we make multi-structural systems and multi-functional with tunable physicochemical properties.
Ionic liquids are superior to organic solvents because they do not produce unwanted by-products and is considered a green replacement for their reusability. In addition, they will significantly improve the biopolymer miscibility with other materials while maintaining the mechanical properties of the biopolymer in the final product. Understanding and controlling the physicochemical properties of the biopolymer in an ionic liquid matrix will be very important for the progress leading to the ability to create powerful multi-level 1D structural fiber material.
It will also help to predict the relationship between fiber and protein secondary structure conformation or carbohydrate crystallinity, thereby creating potential applications for cell growth signaling, ionic conductivity, liquid diffusion and thermal conductivity, and some applications in the biomedical and environmental sciences. It will also enable the regeneration of the biopolymer composite fiber materials with useful functionality and a customized selection is important for additive manufacturing.
Specific skills fiber materials have proven to vary based on their fabrication methods including electrospinning and post-treatment. This review serves to provide basic knowledge is commonly used in protein and polysaccharide biopolymer and method of fabrication of their fiber from a variety of ionic liquids, as well as the effect of post-treatment on fiber materials and their applications in biomedical research and pharmaceuticals, wound healing, filter environmental and chemical research sustainable and green.
Increased absorption of phenol solution using a modified silver nanoparticles Palm Kernel Shell Activated Carbon
Modified Palm Kernel Shell Activated Carbon (PKSAC) use silver nanoparticles (Ag-NP-PKSAC) investigated the uptake of phenol from aqueous solution. The effect of temperature (500-700 ° C), time (90-120 minutes), and alkali concentration (0.1-0.5 M) were studied on yield and methylene blue number for synthesis.
The influence of the initial concentration (100-200 mg / L), agitation (150-250 rpm), the contact time (30-120 minutes), and adsorbent dosage (0.15 to 0.25 g) were studied in batch experiments on the percentage elimination of phenol , MCC, char, PKSAC and Ag-NP-PKSAC characterized using BET, FTIR, SEM, and the proximate analysis. Synthesis PKSAC optimum at 608 ° C, 0.5 M KOH, and carbonization holding time of 60 minutes.
Description: The Brucella IgM Antibody ELISA Test Kit has been designed for the the detection and the quantitative determination of specific IgM antibodies against Brucella in serum and plasma.
Description: Quantitative sandwich ELISA for measuring Human Brucella Antibody IgM (Brucella-Ab-IgM) in samples from cell culture supernatants, serum, whole blood, plasma and other biological fluids.
ELISA kit for Human Brucella Antibody IgM (Brucella-Ab-IgM)
Description: Quantitative sandwich ELISA for measuring Human Brucella Antibody IgM (Brucella-Ab-IgM) in samples from cell culture supernatants, serum, whole blood, plasma and other biological fluids.
ELISA kit for Human Brucella Antibody IgM (Brucella-Ab-IgM)
Description: Quantitative sandwich ELISA for measuring Human Brucella Antibody IgM (Brucella-Ab-IgM) in samples from cell culture supernatants, serum, whole blood, plasma and other biological fluids.
Description: The membrane of this plate has a consistent physical structure with a smooth surface morphology, this makes it ideal for use in bead based assays as the microspheres do not get trapped in the membrane, allowing for efficient bead recovery. The filter plate is suggested no more than 350μL and no less than 1.2μm loading.
AssayStar 384 Square Well Assay Plate, Black Solid Bottom - 100 plates
Description: Qualitativeindirect ELISA kit for measuring Human brucella antibody (IgM) in samples from serum, plasma. A new trial version of the kit, which allows you to test the kit in your application at a reasonable price.
Description: Qualitativeindirect ELISA kit for measuring Human brucella antibody (IgM) in samples from serum, plasma. Now available in a cost efficient pack of 5 plates of 96 wells each, conveniently packed along with the other reagents in 5 separate kits.
Description: This product includes one 96-well plate with 96 protein folding solutions, 0.5 ml in each well of the mother plate; 1.4 ml of Inclusion Body Solubilizer; 4 ml of Neutralizer. Each experiment uses 0.1 ml of the solutions from the mother plate. Each mother plate contains 0.5 ml of solutions in each well and can be used for multiple experiments of folding various proteins.
96 Well ELISA Plate, 8-Well, Detachable, High Binding, White Frame & CLear Well,
Phenol optimum absorption was 85.64, 90.29 and 91.70% for PKSAC, Ag-NP-PKSAC and commercial adsorbents, respectively. The mechanism of phenol adsorption followed Langmuir isotherm and best described as a physio-absorption by the pseudo-second-order kinetics. Phenol showed high affinity (ΔS ° = 0.0079 kJ / mol K) for Ag-NP-PKSAC with favorable adsorption (AG ° = -1.551 kJ / mol) at high temperature for the endothermic (ΔH ° = 1.072 kJ / mol) properties system. The results obtained in this study compares favorably with literature.
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