A new procedure for detecting HRP in nerve tissue is described which is based on the use of pyrocatechol to stabilize the oxidation products of o-tolidine and o-dianisidine in citric acid/ammonium acetate buffer of pH 4.85. In both cases the precipitate obtained is insoluble, stable and more visible than when any variant of the diaminobenzidine method is employed, and the morphological image of neurons and nerve fibres labelled with HRP is superior to that produced by the tetramethylbenzidine/sodium nitroprusside method. There is no non-specific precipitation, and no retraction of nerve tissue has been observed. The performance of the method is improved further using either o-tolidine/pyrocatechol or o-dianisidine/pyrocatechol in conjunction with glucose oxidase, which may be useful if it is desired to obtain Golgi-like images of HRP-bearing cells or to display weakly HRP-labelled nerve fibres.
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Molecules
December 2023
State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022, China.
Porous covalent organic frameworks (COFs) have been widely used for the efficient removal of iodine from solution due to their abundance of electron-rich sites. In this study, two kinds of ketoenamine-based COFs, TpBD-(OMe) and TpBD-Me, are successfully synthesized via Schiff base reaction under solvothermal conditions using 1, 3, 5-triformylphoroglucinol as aldehyde monomer, o-tolidine and o-dianisidine as amino monomers. The ability of TpBD-(OMe) and TpBD-Me to adsorb iodine in cyclohexane or aqueous solutions has been quantitatively analyzed and interpreted in terms of adsorption sites.
View Article and Find Full Text PDFMolecules
January 2012
School of Industrial Technology, University Sains Malaysia, Penang 11800, Malaysia.
The phenolic Schiff bases I-VI were synthesized by condensation reactions between various diamines, namely o-dianisidine, o-tolidine and ethylenediamine with vanillin or p-hydroxybenzaldehyde and subsequent reactions between these phenolic Schiff bases and epichlorohydrin to produce new diglycidyl ethers Ia-VIa. The structures of these compounds were confirmed by CHN, FT-IR, (1)H-NMR, and (13)C-NMR spectroscopy. Their thermotropic liquid crystalline behavior was studied using differential scanning calorimetry (DSC) and polarizing optical microscopy (POM).
View Article and Find Full Text PDFAnal Chim Acta
August 2009
Department of Chemistry, Rani Durgavati University, Jabalpur 482001, Madhya Pradesh, India.
Liquid-phase microextraction (LPME) has been investigated for trace analysis in the present work in conjunction with fibre-optic-based micro-spectrophotometry which accommodates sample volume of 1 microL placed between the two ends of optical fibres. Methods have been evolved for the determination of (i) 1-100 microM and 0.5-20 microM of thiols by single drop microextraction (SDME) and LPME in 25 microL of the organic solvent, respectively, involving their reaction with the Ellman reagent and ion pair microextraction of thiolate ion formed; (ii) 70 microg to 7 mg L(-1) of chlorine/chlorine dioxide by headspace in-drop reaction with alternative reagents, viz.
View Article and Find Full Text PDFEnviron Mol Mutagen
June 2007
Department of Biology, The University of Memphis, Memphis, Tennessee, USA.
4-Aminobyphenyl (4-Ab), benzidine (Bz), and Bz congeners were evaluated for their ability to induce genotoxicity through an oxidative mechanism. The mutagenicity of these compounds was tested in the presence and absence of Aroclor 1254-induced rat S9 mix using Salmonella typhimurium tester strain TA102, which is sensitive to agents producing reactive oxygen species (ROS). In the presence of S9, 4-Ab, Bz, N-acetyl-benzidine, and 3,3-dimethoxybenzidine were strongly mutagenic in TA102, whereas, 3,3,5,5-tetra-methylbenzidine, 3,3-dimethylbenzidine (O-tolidine), and N,N-diacetylbenzidine were not mutagenic.
View Article and Find Full Text PDFToxicol Lett
June 2004
Institut für Arbeitsphysiologie an der Universität Dortmund, Ardeystr. 67, D-44139 Dortmund, Germany.
In the past, azo colorants based on benzidine, 3,3'-dichlorobenzidine, 3,3'-dimethylbenzidine (o-tolidine), and 3,3'-dimethoxybenzidine (o-dianisidine) have been synthesized in large amounts and numbers. Studies in exposed workers have demonstrated that the azoreduction of benzidine-based dyes occurs in man. The metabolic conversion of benzidine-, 3,3'-dimethylbenzidine- and 3,3'-dimethoxybenzidine-based dyes to their (carcinogenic) amine precursors in vivo is a general phenomenon that must be considered for each member of this class of chemicals.
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