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Sodium triphosphate

Manufactured by Merck Group
Sourced in United States, Germany

Sodium triphosphate is a chemical compound with the formula Na5P3O10. It is a white, crystalline solid that is soluble in water. Sodium triphosphate is used as a sequestering agent, water softener, and detergent builder in various industrial and household applications.

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8 protocols using sodium triphosphate

1

Acetylcholinesterase Inhibition Assay

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Acetylcholinesterase from electric eel, lyophilized powder (≥1000 units/mg protein), acetylthiocholine chloride (ATChCl), 5,5′-dithiobis(2-nitrobenzoic acid) (DTNB), GA solution (50%), galanthamine hydrobromide, carbofuran (98%), phosphate buffer saline (PBS) pH 7.4, isopropyl alcohol (i-PrOH), dimethyl sulfoxide (DMSO), tetraethyl orthosilicate (TEOS), 3-aminopropyltriethoxysilan (APTES), N1-(3-Trimethoxysilylpropyl)diethylenetriamine (BAATMS), sodium borohydride, ammonia, iron(III) nitrate nonahydrate, sodium triphosphate, and calcium nitrate tetrahydrate were purchased from Sigma-Aldrich (St. Louis, MO, USA). Ethanol (EtOH), methanol (MeOH), sodium acetate and acetic acid were obtained from PENTA (Prague, Czech Republic). SWV assay was performed using electrochemical device PalmSens (PalmSens BV, Houten, The Netherlands) connected with computer and operated by software PSTrace 4.8.1 (PalmSens BV, Houten, The Netherlands). Screen-printed sensors (Metrohm, Herisau, Switzerland) were sized 34 × 10 × 0.5 mm with a 4 mm diameter carbon working electrode, silver reference electrode, and carbon auxiliary electrode.
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2

Multifunctional Nanoparticle Synthesis

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Sodium nitrite, L-cysteine, tetramethylorthosilicate, low molecular weight chitosan, ethanolamine, ferrous chloride (FeCl2), ferric chloride (FeCl3) anhydrous, sodium triphosphate, and hydrochloric acid were purchased from Sigma-Aldrich (Germany). All other solvents and reagents were of high purity and used as received.
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3

Astaxanthin-Loaded Chitosan Nanoparticles

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Chitosan (CS, 50–190 kDa, 24 cps, 95% deacetylated), sodium triphosphate (TPP), 2,2-Diphenyl-1-pikryl-hydrazyl (DPPH), linoleic acid, and sodium dodecyl sulfate (SDS) were purchased from Sigma-Aldrich Co. (St. Louis, MO, USA). Astaxanthin (ASX) was obtained from Neo Cremar Co. (Sungnam, Korea). Baby hamster kidney (BHK)-21 cells were obtained from the Korean Cell Line Bank (Seoul, Korea). Dulbecco’s Modified Eagle’s culture medium (DMEM) and fetal bovine serum were obtained from Gibco Invitrogen Co. (Grand Island, NY, USA). Penicillin-streptomycin and phosphate-buffer saline (PBS) were obtained from Lonza (Walkersville, MD, USA). 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) was purchased from Sigma-Aldrich Co. (St. Louis, MO, USA). All other chemicals were of reagent grade, and all solvents were of HPLC grade.
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4

Antioxidant Compound Extraction and Analysis

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Chitosan, 2,2-diphenyl-1-picrylhydrazyl (DPPH), 2,2-azinobis-(3-ethylbenzothiazoline-6-sulfonate) (ABTS), sodium triphosphate (TPP), Folin Ciocalteau reagent, tyrosol, coumaric acid, ferulic acid, were purchased from Sigma-Aldrich (Milan, Italy), luteolin, verbascoside, luteolin-7-O-glucoside, rutin, oleuropein, luteolin-4-O-glucoside, ligstroside, luteolin all purchased from Extrasynthése (Genay, Francia).
B’cuzz Hydro A + B nutrient solution (A: N-P-K 5-0-5; Nitrogen (N) 4.85%, Phosphorus pentoxide (P2O5) 0.15%, Potassium Oxide (K2O) 4.73%, Sodium Oxide (Na2O) 0.19%, Calcium Oxide (CaO) 3.79%, Magnesium Oxide (MgO) 1.32%, Sulfur Trioxide (SO3) 0.11%, Iron (Fe) 0.040%, Boron (B) 0.001%; B: N-P-K 0-4-6; Nitrogen (N) 0.68%, Phosphorus pentoxide (P2O5) 4.07%, Potassium Oxide (K2 O) 5.71%, Sodium Oxide (Na2O) 0.20%, Calcium Oxide (CaO) 0.25%, Magnesium Oxide (MgO) 0.71%, Sulfur Trioxide (SO3) 0.94%, Manganese (Mn) 0.029%, Copper (Cu) 0.001%, Zinc (Zn) 0.039%, Molybdenum (Mo) 0.001%, Boron (B) 0.012%) ATAMI, Rosmalen, Netherlands.
All of the reagents for microbiology were used and provided by Oxoid Limited (Basingstoke, UK). All of the solvents for the high-performance liquid chromatography were used and provided by VWR International Srl (Milan, Italy). Moreover, all of the chemicals were used at 99% purity.
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5

Fibroblast Cell Proliferation Assay

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Acetone (97%), polyethylene oxide (PEO; MW = 300,000), cerium(III) nitrate hexahydrate (Ce(III)), phosphate-buffered saline, sodium triphosphate, Tris-buffered saline (TBS), and dichloromethane (DCM) were purchased from Sigma-Aldrich (St. Louis, MO, USA). Human dermal fibroblasts (PCS-201-012) and cell culture reagents were purchased from American Type Culture Collection (ATCC; Manassas, VA, USA). CyQUANT® cell proliferation assay kits were purchased from Thermo Fisher Scientific (Waltham, MA, USA).
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6

Synthesis and Evaluation of Hexahydrocurcumin

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Chitosan (CS, 75 kDa, 84.3 ± 0.2% deacetylated) was provided by Marine Bio-Resources Co., Ltd. (Samut Sakhon, Thailand). Sodium triphosphate (TPP), 1,1-diphenyl-2-picrylhydrazyl (DPPH), 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT), Pluronic® F-127mucin powder from porcine stomach Type III, α-amylase, porcine lipase Type II and bile extract powder, pepsin from hog stomach, pancreatin from hog pancreas, and albumin from human serum (HSA) and bovine serum (BSA) were purchased from Sigma-Aldrich Co., Ltd. (St. Louis, MO, USA). Fetal bovine serum (FBS) was obtained from Life Science Production (LPS, Bedford, UK). Serum-free Dulbecco’s modified Eagle’s medium (DMEM) was purchased from Invitrogen Cop. (Grand Island, NY, USA). Hexahydrocurcumin (HHC) was synthesized from curcumin (Cur) following the method described by Srimuangwong et al. [15 (link)]. Wright-Giemsa dye was purchased from M&P IMPEX Ltd. (Ladkrabang, BKK, Thailand). Analytical grades of acetic acid, acetone, absolute ethanol, hydrogen peroxide, and dimethyl sulfoxide (DMSO) were purchased from Carlo Erba reagents (Val de Reuil, France). Ultrapure water was obtained from the Thermo Scientific Barnstead MicroPure system (Thermo Fisher Scientific Inc., Waltham, MA, USA). Other reagents were used without further purification.
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7

Alginate-Chitosan Cytotoxicity Assay

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Sodium alginate (medium viscosity, Sigma, Saint Louis, MO, USA), chitosan (low molecular weight, ≥75% deacetylation, Sigma), Thiazolyl Blue Tetrazolium Bromide (Sigma), and sodium triphosphate (TPP, Merck, Rahway, NJ, USA) were purchased from a local supplier (Alborz Shimi Co., Tehran, Iran). Phosphate-buffered saline, 4,6-diamidino-2-phenylindole dihydrochloride (Invitrogen, Waltham, MA, USA), acridine orange ethidium bromide (Invitrogen) were provided by KalaZist Co. (Tehran, Iran). All reagents were analytical grades.
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8

Meagre Fish Ham Preparation

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Farmed meagre (Argyrosomus regius) was captured from IPMA Aquaculture Research Station at Olhão, Portugal (EPPO) and slaughtered by immersion on an ice and sea water (1 kg:1 L) bath. The fish were kept in ice and transported to the laboratory within 24 h. The individual fish weight was 376 ± 111 g. Fish was processed (headed, tailed, gutted, and filleted) at low temperature (below 10 °C) and, after filleting, meagre was minced in a 694 BAADER meat deboner (BAADER, Lübeck, Germany) equipped with a 3 mm diameter hole rotating cylinder.
The remaining ingredients used for the preparation of fish hams were all of food grade materials manufactured by different companies, as specified in Table 1. Sodium triphosphate was of analytical grade from Merck (Darmstadt, Germany). Sodium triphosphate was used as fat/protein stabilizer acting on protein crosslinking, controls pH and removes traces of iron and reduces sensitization to discoloration. Sodium chloride was used to increase the solubility of the proteins and crosslinking. Sodium nitrite was used for color fixation, imparting flavor and characteristic aromas, reduces lipid oxidation and inhibits growth of Clostridium botulinum. Casings and packages used were of food grade.
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