2002
DOI: 10.1016/s0003-2697(02)00210-5
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Specific and instantaneous one-step chemodetection of histidine-rich proteins by Pauly's stain

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Cited by 17 publications
(22 citation statements)
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“…1b). Some of the protein bands were positive for Pauly's stain, indicating the presence of His-rich polypeptides 21 . In addition, nitroblue tetrazolium (NBT) staining showed that the smaller proteins contained catecholic residues, whereas a lectin-binding assay confirmed the presence of chitin oligomers in the highermolecular-weight fractions.…”
Section: Gigas Chitin-binding Beak Proteinsmentioning
confidence: 99%
See 1 more Smart Citation
“…1b). Some of the protein bands were positive for Pauly's stain, indicating the presence of His-rich polypeptides 21 . In addition, nitroblue tetrazolium (NBT) staining showed that the smaller proteins contained catecholic residues, whereas a lectin-binding assay confirmed the presence of chitin oligomers in the highermolecular-weight fractions.…”
Section: Gigas Chitin-binding Beak Proteinsmentioning
confidence: 99%
“…Proteins were separated by gel electrophoresis by Tricine-SDS-PAGE using 4% stacking and 16% resolving gels, prepared as previously described 46 , and then stained either with Coomassie Blue R-250 (CBR) stain 46 , Pauly's stain 21 or nitroblue tetrazolium (NBT) stain 47 , which stain for generic proteins, His-rich and catecholic proteins, respectively. Approximately 10 μg of proteins were loaded in each lane for CBR stain and 30 μg for Pauly's stain and NBT, unless otherwise stated.…”
Section: Gel Electrophoresismentioning
confidence: 99%
“…[39] Property contour maps were generated using the Origin graphing software (OriginLab, Northampton, MA, USA). Pauly's solution [40] , which specifically stains for His-rich proteins. Prior to Pauly's staining, gels were rinsed in isopropanol and water in order to remove the residual SDS, a prerequisite for the staining technique.…”
Section: Microscopy (Sem) and Energy Dispersive Spectroscopy (Eds) Amentioning
confidence: 99%
“…A total of 4 µg of each AGP fraction was dot‐blotted onto a 0.22 µm nitrocellulose membrane (Osmonics Inc., Westborough, MA) and then air‐dried. Pauly's stain was applied to the membrane following the methods of Sahal et al (2002) with the following changes: 1% sulfanilic acid (Sigma‐Aldrich) and 5% sodium nitrate were chilled and an equal volume of both solutions was mixed while still cold. The mixture was sprayed lightly, without forming pools of stain, onto the membrane which was pre‐wet with MilliQ water.…”
Section: Methodsmentioning
confidence: 99%