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P phenylenediamine ppd

Manufactured by Merck Group
Sourced in United States

P-phenylenediamine (PPD) is a laboratory chemical used as a reagent in various analytical and research applications. It is a colorless crystalline solid with the chemical formula C6H8N2. PPD is commonly used as a developer in photography, as a component in hair dyes, and as an intermediate in the synthesis of other organic compounds. Its core function is as a chemical reagent in laboratory settings, without extrapolation on intended use.

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5 protocols using p phenylenediamine ppd

1

Yeast Transformation and Enzyme Assay

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Yeast Transformation Kit, 2,6-dimethoxyphenol (DMP), N,N-dimethyl-1,4-phenylenediamine (DMPD), 5-Hydroxyimino-2,4,6(1H,3H,5H)-pyrimidinetrione (violuric acid), Evans Blue (EB), Reactive Black 5 (RB5), aniline, p-phenylenediamine (PPD) and HBT were purchased from Sigma-Aldrich (St. Louis, MI, USA). High Pure Plasmid Isolation Kit and 2,2′azinobis (3 ethylbenzothiazoline-6 sulphonic acid) (ABTS) were obtained from ROCHE (Basel, Switzerland). Detergents: polyoxyethylene (10) tridecyl (PET), TWEEN 20 and CHAPS were purchased from Sigma-Aldrich (St. Louis, MI, USA). Phusion High-Fidelity DNA polymerase and Restriction enzymes were purchased from New England Biolabs (Ipswich, MA, USA). QIAquick gel extraction kit from Qiagen (Hilden, Germany). ZymoprepTM Yeast Plasmid Miniprep II was purchased from Zymo Research (Irvine, CA, USA). S. cerevisiae BJ5465 strain was purchased from LGC Promochem (Teddington, UK) and Mutazyme II DNA polymerase was from Agilent (Santa Clara, CA, USA). Agrocybe pediades AH40210 was obtained from the University of Alcalá Herbarium Culture Collection, Alcalá de Henares, Spain.
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2

Robust Tissue Preparation and Imaging

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ON tissue (n = 10 per group) was collected and fixed in 4% EM-grade PFA (Electron Microscopy Sciences, Hatfield, PA, USA) in PBS then 2% glutaraldehyde in 0.1M cacaodylate buffer for 2 h on ice, then post fixed in 2% osmium tetroxide in cacodylate buffer and dehydrated in ascending concentrations of 200-proof ethanol (50%, 70%, 95%, 100%) and further dehydrated in propylene oxide. ON tissue was embedded in Epon epoxy resin (Electron Microscopy Sciences) and 1 μm thick semi-thin sections cut using Leica Microtome and stained with 1% p-phenylenediamine (PPD) (Sigma-Aldrich Corp., St. Louis, MO, USA) and 1% toluidine blue (Fisher, Watham, Massachusetts, USA). Slides were imaged using 100x oil emersion objective on AxioPlan 2 microscope (Carl Zeiss) and manually compiled using the photomerge function in Adobe Photoshop (Adobe Systems Inc., San Jose, CA, USA).
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3

Gadolinium-Based Theranostic Nanoparticles

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All chemicals and solvents were obtained from commercial sources and used without further purification. p-Phenylenediamine (pPD, Sigma Aldrich, Cat# 78429), Citric acid (CA, Sigma Aldrich, Cat# 251275), Gadolinium nitrate hexahydrate (Gd(NO3)3∙6H2O, Sigma Aldrich, Cat# 211591), Ethanol (KOPTEC, Cat# 19J14D), Dialysis membrane (Spectrum, [MWCO] = 100–500), Milli-Q H2O, 3-(4,5-Dimethylthiazolyl-2)-2,5-diphenyltetrazolium bromide (MTT) (Sigma Aldrich, Cat# M2128).
All experimental procedures involving animals were executed accordance with animal protocol approved by University of North Carolina at Chapel Hill Institutional Animal Care and Use Committee.
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4

Gadolinium-Based Nanoparticle Synthesis

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P-phenylenediamine (pPD) (Sigma Aldrich, Cat# 78429), gadolinium nitrate hexahydrate (Gd(NO3)3∙6H2O, Sigma Aldrich, Cat# 211591), ethanol (KOPTEC, Cat# 19J14D), dialysis membrane (Spectrum, MWCO=100–500), Milli-Q H2O, 3-(4,5-dimethylthiazolyl-2)-2,5-diphenyltetrazolium bromide (MTT) (Sigma Aldrich, Cat# M2128).
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5

Fabrication of Ni-pPD@rGO Nanosheets

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GO suspensions (5 mg/ml) were first fabricated according to the modified Hummer’s method43 (link),44 (link). A solution of 1.92 g (6.6 mmol) of Ni(NO3)·6H2O in 28 ml of Milli-Q water was mixed with 32 ml GO suspension in a sealed three-necked flask. Another solution of 1.57 g (14.5 mmol) of p-phenylenediamine (pPD) (Sigma Aldrich) in 60 ml of Milli-Q water was also prepared in a sealed flask. Two solutions were separately stirred and purged with Ar gas for 1 h to exclude any external oxygen sources in the solutions. Two solutions were then mixed together in the three-necked flask and 20 ml of concentrated NH4OH solution was added drop by drop to initiate the reaction. During the reaction, the mixture was stirred in a sealed flask with Ar gas bubbling for over 10 h at room temperature. The resulted black powders were filtered and then washed with Milli-Q water and ethanol thoroughly. Finally, the solids were redispersed into 200 ml Milli-Q water to make Ni-pPD@rGO suspensions (0.6 mg ml–1). For comparison, Ni(OH)2@GO nanosheets were also synthesized by treating GO only with Ni(NO3)2 and NH4OH (without adding the pPD solution).
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