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Glycol chitosan

Manufactured by Merck Group
Sourced in United States, Italy, Sao Tome and Principe

Glycol chitosan is a water-soluble derivative of the natural polysaccharide chitosan. It is a biocompatible and biodegradable material commonly used in various research and laboratory applications.

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40 protocols using glycol chitosan

1

Glycol Chitosan-EGCG Hydrogel Synthesis

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Initially, 3% (w/v) glycol chitosan (Molecular Weight degree of polymerization > 400, 60% titration; Sigma Aldrich, USA) solution was prepared by dissolving 300 mg of glycol chitosan in 10 mL of distilled water. Then, the EGCG (LG Healthcare, Republic of Korea) monomers were dissolved in Dimethyl sulfoxide (purity ≥99.9%, anhydrous, Sigma Aldrich, USA) at 42 mM, 98 mM, and 154 mM. Three different concentrations of EGCG solutions were diluted in 3% (w/v) glycol chitosan solutions to 3 mM, 7 mM, and 11 mM, respectively. Then, the SA_Ty stock solution was added to 5 μM. Pre-gel solutions were cross-linked for 3 h. Cross-linking time was verified by tilting vials until the flow of solutions was not observed.
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2

Glycol Chitosan-Based Curcumin Delivery System

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Glycol chitosan (GC, ≥60% (by titration), crystalline, Mw ≅ 585,000 g/mol), glycidyl methacrylate (GM), and curcumin (CUR) were purchased from Sigma-Aldrich (St. Louis, MO, USA). 4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride (DMT-MM) was obtained from Wako Pure Chemical Industries, Ltd. (Osaka, Japan). Dialysis tubing (Spectrum Laboratories Inc., Rancho Dominguez, CA, USA) was used for purification. The mouse L-929 fibroblast cell line was supplied by Korean Cell Line Bank (Seoul, Korea). All the chemicals were used as received without further purification.
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3

SDS-PAGE Protein Activity Assay

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The protein samples were added to SDS–PAGE sample buffer and heated at 100°C for 15 min. The proteins were separated on a 10% polyacrylamide gel containing 0.01% glycol chitosan (Sigma-Aldrich, St. Louis, MO, United States). The gel was cut into two parts; the negative control was not immersed in a refolding buffer, and the other part of the gel was immersed in a refolding buffer (50 mM Tris–HCl pH 7.5, 1% Triton X-100) at 37°C overnight. The gel was washed with distilled water and then stained with 0.01% (w/v) calcofluor white M2R in 10 mM Tris–HCl (pH 7.5). After 5 min, the brightener solution was removed, and the gel was washed with distilled water. Protein activity was visualized by placing the gels on a UV transilluminator (Trudel and Asselin, 1989 (link)). The two parts of the gel were photographed together.
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4

Chitin-Based Antioxidant Assays

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Chitin (from shrimp shells, coarse flakes), glycol chitosan, GlcNAc and biotin were from Sigma Aldrich (St. Louis, MO, USA). Chitosan CHIT100 and CHIT600 (both from shrimp shells) were from Acros Organics (Thermo Fischer Scientific Inc., Waltham, MA). Chitosan QS2 (from Pandalus borealis) was from InFiQuS (Madrid, Spain). Colloidal Chitin, glycol Chitin and chitosan solutions were obtained as explained previously [20 (link)]. ABTS (2,2′-azino-bis (3-ethylbenzothiazoline-6-sulfonate), DPPH (2,2-diphenyl-1-picrylhydrazyl), N,N′, -di-acetyl-glucosamine ((GlcNAc)2), N,N′,Nʺ -tri-acetyl-glucosamine ((GlcNAc)3) and N,N′,Nʺ,N′ʺ -tetra-acetyl-glucosamine ((GlcNAc)4) were from Carbosynth Ltd. (Berkshire, UK). Yeast Nitrogen Base w/o amino acids (YNB) was from Difco (BD, Sparks, MD, USA). All reagents were of the highest purity grade.
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5

Nisin A-Based Antimicrobial Hydrogel Synthesis

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Nisin A (95%, isolated from Lactococcus lactis in sauerkraut) was obtained from Handary, Belgium. Dextran (from Leuconostoc mesenteroides, 100–200 kDa), Dextran 60 (from L. mesenteroides, ~ 60 kDa), alginic acid (from brown algae, low viscosity (4–12 cps), M/G ratio 1.43 as determined by 13C SS-NMR below), sodium (meta) periodate (> 99%), ethylene glycol (99%), N-hydroxysulfosuccinimide sodium salt (S-NHS, > 98%), N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (EDC, crystalline), adipic acid dihydrazide (ADH, > 98%), hydroxylamine hydrochloride, glycol chitosan (degree of deacetylation: > 60%), trifluroacetic acid (TFA, > 99%), acetonitrile (ACN, > 99.9%), phosphate-buffered saline (tablets, PBS), and sodium dodecyl sulphate were all purchased from Sigma-Aldrich, Ireland. Dimethyl sulfoxide (DMSO, for molecular biology) was purchased from VWR International. Liquid nitrogen was supplied by BOC Gases (Ireland). Glycine (lab grade), 2,4,6-trinitrobenzene sulfonic acid (5% w/v, MeOH), potassium chloride (99%) and hydrochloric acid (37%, fuming) were purchased from Fisher Scientific, Ireland. Pullulan/Dextran standards for light scattering/tetra detection (TDS3030) were provided by Particular Sciences, Dublin, Ireland. Staphylococcus aureus (DSM 20231) was purchased from the Leibniz Institute DSMZ-German collection of Microorganisms and Cell Cultures.
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6

Glycol Chitosan-Based Bone Tissue Engineering

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Glycol chitosan (GC, B100 kDa), glycidyl methacrylate (GMA), lysozyme from chicken egg white, tween-20, p-nitrophenol phosphate, β-glycerophosphate, L-ascorbic acid, dexamethasone, riboflavin (RF), nitro blue tetrazolium (NBT), 5-bromo-4-chloro-3-indoxylphosphate, alizarin red S and ethylene diaminetetraacetic acid (EDTA) were supplied by Sigma-Aldrich (St. Louis, MO). Low glucose dulbecco’s modified eagle’s medium (DMEM), penicillin/streptomycin (P/S, 100 U mL−1) and trypsin were purchased from Life Technologies (Grand Island, NY). Fetal bovine serum (FBS) was obtained by Mediatech Inc. (Manassas, VA). All solvents and products were used without further purification.
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7

Glycol Chitosan-based Magnetic Nanoparticle Conjugates

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Glycol chitosan (250 kDa molecular weight, degree of deacetylation > 60%), 5β-cholanic acid, N-(3-dimethylaminopropyl)-N’-ethylcarbodiimide hydrochloride (EDC), and N-Hydroxy-Succinimide (NHS) were purchased from Sigma-Aldrich (St. Louis, MO). Monoreactive hydroxysuccinimide ester of Cyanine 5.5 (Cy5.5-NHS) was obtained from Lumiprobe (Hallandale Beach, FL). Biotin-4-fluorescein (B4F) was obtained from Biotium (Hayward, CA). Superparamagnetic iron oxide nanoparticles (nano-screenMAG-ARA, nano-screenMAG-Streptavidin) were purchased from Chemicell (Germany). These magnetic nanoparticles (MNPs) consist of a magnetite core covered by a fluorescence layer (λem,max= 413 nm or 613 nm). Anti-LKB1 and SAD-antibodies were from EMD Millipore (Billerica, MA). Anti-FLAG®M2 antibody was from Sigma (St. Louis, MO). Neuronal Class III β-Tubulin (Tuj1) antibody and pan-axonal neurofilament marker SMI-312, were purchased from Covance (Princeton, NJ). Anti-STRAD, anti-Tau, and phospho-site-specific antibody for Tau at Ser-262, were purchased from Santa Cruz Biotechnology (Santa Cruz, CA). Anti-β-actin antibody was from Cell Signaling Technology (Danvers, MA).
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8

Glycol Chitosan-Doxorubicin Conjugate Synthesis

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Glycol chitosan (MW = 250 kDa; degree of deacetylation > 60%), doxorubicin hydrochloride (DOX-HCl), 5β-cholanic acid, 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide hydrochloride (EDC), N-hydroxysuccinimide (NHS), triethylamine (TEA), anhydrous methanol and anhydrous dimethyl sulfoxide (DMSO) were purchased from Sigma-Aldrich (Merck, Darmstadt, Germany). A fluorescent molecule, Cy5.5-NHS ester, was purchased from Lumiprobe Corporation (Hunt Valley, MD, USA). All other chemicals were purchased as reagent grade and used without further purification or modification.
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9

Apoptosis Assay with GC and RACC

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Glycol chitosan (GC), retinoic acid chlorochalcone (RACC), dialysis membranes (MWCO = 12,000 g/mol) and propidium iodide (PI) were purchased from Sigma Chem. Co. Ltd. (St. Louis, MO, USA). FITC-annexin V was obtained from Santa Cruz, CA, 95060, USA.
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10

Glycol Chitosan-Based Fluorescent Probes

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Glycol chitosan (GC; molecular weight, 2.5 × 105 Da; the degree of deacetylation, 82.7%), 5β-cholanic acid, N-hydroxysuccinimide (NHS; purity, >99%), 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide hydrochloride (EDC; purity, >99%), methanol (purity, >99%), and anhydrous dimethyl sulfoxide (DMSO; purity, >99%) were purchased from Sigma Aldrich (St. Louis, MO, USA). The mono-functional hydroxysuccinimide ester of cyanine 5.5 (Cy5.5-NHS) and indocyanine green (ICG-NHS) were purchased from GE Healthcare Life Sciences (Chicago, IL, USA) and Bioacts (Incheon, Korea), respectively. For the cell experiments, the Roswell Park Memorial Institute 1640 (RPMI-1640) medium, Dulbecco’s phosphate buffered saline (DPBS), fetal bovine serum (FBS), antibiotics (penicillin with streptomycin), and trypsin–EDTA were purchased from Welgene. Inc. (Daegu, Korea). All the other chemicals were purchased at reagent grade and used without further purification.
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