Search results for "Staining"

showing 10 items of 449 documents

Improving Biological Dyes and Stains: Quality Testing Versus Standardization

1994

This paper discusses the impact of both standardization and quality testing of dyes and stains in biology and medicine. After the brief review of why standardized dyes and strains are not presently available commercially, two types of testing and ways of improving dye quality are described. National or international organizations could be established to define standardization of dyes and stains. Standardization would be specifically defined as a list of physico-chemical parameters such as elaborated in this paper. Commercial batches of comparable quality may be labeled by the supplier as "standard dye," a procedure currently performed by the European Council for Clinical and Laboratory Stan…

Quality ControlHistologyStaining and LabelingStandardizationHistocytochemistrybusiness.industrymedia_common.quotation_subjectColoring agentsGeneral MedicineCertificationManufacturing engineeringEuropeMedical Laboratory TechnologyBiological stainTesting protocolsHumansMedicineQuality (business)Coloring AgentsDye testingbusinessmedia_commonBiotechnic & Histochemistry
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Cryopreservation of MHC Multimers: Recommendations for Quality Assurance in Detection of Antigen Specific T Cells

2015

Fluorescence-labeled peptide-MHC class I multimers serve as ideal tools for the detection of antigen-specific T cells by flow cytometry, enabling functional and phenotypical characterization of specific T cells at the single cell level. While this technique offers a number of unique advantages, MHC multimer reagents can be difficult to handle in terms of stability and quality assurance. The stability of a given fluorescence-labeled MHC multimer complex depends on both the stability of the peptide-MHC complex itself and the stability of the fluorochrome. Consequently, stability is difficult to predict and long-term storage is generally not recommended. We investigated here the possibility of…

Quality ControlHistologyT-LymphocytesSerum albuminquality assuranceBiologyrecommendations for MHC multimer storageMajor histocompatibility complexcryopreservationEpitopeCryopreservationPathology and Forensic MedicineFlow cytometryCryoprotective AgentsAntigen specificQuantum DotsmedicineHumansFluorescent Dyesmedicine.diagnostic_testStaining and LabelingcryoprotectantHistocompatibility Antigens Class IReproducibility of ResultsCell BiologyMHC multimerFlow CytometryMolecular biologyMHC multimerBiochemistrybiology.proteinSpecial Section : Improving Methods for Blood Cell AnalysisIndicators and Reagentsglycerol in T cell stainingProtein MultimerizationPeptidesCytometry
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Uptake of silica covered Quantum Dots into living cells: Long term vitality and morphology study on hyaluronic acid biomaterials

2015

Quantum Dots (QDs) are promising very bright and stable fluorescent probes for optical studies in the biological field but water solubility and possible metal bio-contamination need to be addressed. In this work, a simple silica-QD hybrid system is prepared and the uptake in bovine chondrocytes living cells without any functionalization of the external protective silica shield is demonstrated. Moreover, long term treated cells vitality (up to 14 days) and the transfer of silica-QDs to the next cell generations are here reported. Confocal fluorescence microscopy was also used to determine the morphology of the so labelled cells and the relative silica-QDs distribution. Finally, we employ sil…

Quantum DotNanoparticleBiocompatible Materials02 engineering and technology01 natural scienceschemistry.chemical_compoundNanoparticleLabellingHyaluronic acidFluorescence microscopeLong term cell stainingBiocompatible MaterialSilicon Dioxide021001 nanoscience & nanotechnologyMechanics of MaterialsSelf-healing hydrogelsMaterials Science (all)0210 nano-technologySilica Quantum DotMaterials scienceFluorescence confocal microscopyCell SurvivalSilicon dioxideChondrocyte bovine cellHyaluronic acidConfocalBioengineeringNanotechnologyCondensed Matter Physic010402 general chemistryBiomaterialsChondrocytesQuantum DotsAnimalsMechanics of MaterialCell ShapeSilica Quantum DotsAnimalMechanical Engineeringtechnology industry and agricultureChondrocyteequipment and suppliesSettore FIS/07 - Fisica Applicata(Beni Culturali Ambientali Biol.e Medicin)0104 chemical sciencesMicroscopy FluorescencechemistrySettore CHIM/09 - Farmaceutico Tecnologico ApplicativoQuantum dotBiophysicsNanoparticlesSurface modificationCattleMaterials Science and Engineering: C
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Mboat7 down-regulation by hyper-insulinemia induces fat accumulation in hepatocytes.

2020

Background: Naturally occurring variation in Membrane-bound O-acyltransferase domain-containing 7 (MBOAT7), encoding for an enzyme involved in phosphatidylinositol acyl-chain remodelling, has been associated with fatty liver and hepatic disorders. Here, we examined the relationship between hepatic Mboat7 down-regulation and fat accumulation. Methods: Hepatic MBOAT7 expression was surveyed in 119 obese individuals and in experimental models. MBOAT7 was acutely silenced by antisense oligonucleotides in C57Bl/6 mice, and by CRISPR/Cas9 in HepG2 hepatocytes. Findings: In obese individuals, hepatic MBOAT7 mRNA decreased from normal liver to steatohepatitis, independently of diabetes, inflammatio…

Research paperTGFβ Transforming Growth Factor BetaIntracellular SpaceCRISPR Clustered Regularly Interspaced Short Palindromic RepeatshHEPS Human HepatocytesMice0302 clinical medicineLPIAT1DAG Diacylglyceroli.p. Intraperitonealmedia_commonFatty AcidsGeneral Medicine3. Good health030220 oncology & carcinogenesisHOMA-IR homeostasis Model Assessment of Insulin ResistanceMPO morpholinolcsh:Medicine (General)medicine.medical_specialtyPE Phosphatidyl-EthanolamineNashGeneral Biochemistry Genetics and Molecular Biology03 medical and health sciencesTNFα tumor Necrosis Factor AlphaLDL Low Density LipoproteinsHyperinsulinismNAFLDSD Standard Dietmedia_common.cataloged_instanceHumansCPT1 Carnitine Palmitoyltransferase IPhosphatidylinositolGene SilencingEuropean unionVLDL Very Low Density Lipoproteinlcsh:RhHSC Human Hepatic Stellate Cellsmedicine.diseaseLipid MetabolismOA Oleic AcidCI Confidence IntervalMboat7 Membrane bound O-acyltransferase domain containing 7MCD methionine choline deficient diet030104 developmental biologyEndocrinologychemistryCDP Cytidine-DiphosphateFOXO1 Forkhead Box protein O1NAFLD nonalcoholic fatty liver diseaseSteatohepatitisBMI Body Mass IndexCL CardiolipinAcyltransferases0301 basic medicineAlcoholic liver diseaseCXCL10 C-X-C Motif Chemokine 10lcsh:Medicinechemistry.chemical_compoundNon-alcoholic Fatty Liver DiseaseIFG Impaired Fasting GlucoseAPOB Apolipoprotein BNonalcoholic fatty liver diseasePIP Phosphatidyl-Inositol-PhosphateSteatohepatitisqRT-PCR quantitative Real Time Polymerase Chain ReactionMice Knockoutlcsh:R5-920ORO Oil Red O StainingPI PhosphatidylinositolFatty liverTM6SF2 Transmembrane 6 Superfamily Member 2PhospholipidTAG TriglyceridesNASH Nonalcoholic SteatohepatitisLipogenesisLPA Lyso-Phosphatidic AcidPhosphatidylinositolSignal TransductionPS Phosphatidyl-SerinePA Palmitic AcidALD alcoholic liver diseasePC Phosphatidylcholinei.v. IntravenousFATP1 Fatty Acid Transport Protein 1Models BiologicalInternal medicinemedicineAnimalsNonalcoholic fatty liver diseasePPARα Peroxisome Proliferator-Activated Receptor alphaObesityG3P Glyceraldehyde-3-PhosphateSREBP1c Sterol Regulatory Element-Binding Protein 1HDL High Density Lipoproteinsbusiness.industryPI3K Phosphatidylinositol 3 KinaseMembrane ProteinsNHEJ Non-Homologues End JoiningPNPLA3 Patatin-like Phospholipase Domain-containing-3MTTP Microsomal Triglyceride Transfer ProteinLPIAT1 Lysophosphatidylinositol Acyltransferase 1TMC4 Transmembrane Channel-Like 4Disease Models AnimalGene Expression RegulationHepatocytesFOXA2 Forkhead Box A2mTOR mammalian target of RapamycinSteatosisInsulin ResistancebusinessPG Phosphatidyl-GlycerolFABP1 Fatty Acid-Binding Protein 1 FAS Fatty Acid SynthaseT2DM Type 2 Diabetes MellitusEBioMedicine
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Influence of surface treatments on enamel susceptibility to staining by cigarette smoke

2013

Objectives: The purpose of this study was to evaluate the influence of remineralizing agents, including artificial saliva, neutral fluoride, and casein phosphopeptide-amorphous calcium phosphate (CPP-ACP), on the susceptibility of bleached enamel to staining by cigarette smoke. Study Design: Fifty bovine enamel blocks were randomly divided into five groups (n = 10): G1- bleaching; G2- bleaching and immersion in artificial saliva; G3- bleaching and application of CPP-ACP; G4- bleaching and application of neutral fluoride; and G5- untreated (Control). Teeth were bleached with 35% hydrogen peroxide and treated with the appropriate remineralizing agent. After treatment, all groups were exposed …

Salivagenetic structuresDentistryOdontologíachemistry.chemical_compoundstomatognathic systemCaseinClinical and Experimental DentistryMedicineCigarette smokeFood scienceHydrogen peroxideGeneral DentistryEnamel paintbusiness.industryResearchSignificant difference:CIENCIAS MÉDICAS [UNESCO]Ciencias de la saludStainingchemistryvisual_artUNESCO::CIENCIAS MÉDICASvisual_art.visual_art_mediumsense organsbusinessFluoride
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Fine-tuning scaffolds for tissue regeneration: effects of formic acid processing on tissue reaction to silk fibroin

2010

Formic acid (FA) plays a key role in the preparation of silk fibroin (SF) scaffolds from cocoons of Bombyx mori and is used for fibre distribution. In this study, we used a subcutaneous implantation model in Wistar rats to examine SF scaffolds prepared by treating the degummed cocoon with FA for either 30 or 60 min. The tissue reaction and inflammatory response to SF was assessed by qualitative histology at intervals from 3 to 180 days. Additionally, dynamic biomaterial-induced vascularization and biomaterial degradation were quantified using a technique for analysing an image of the entire implanted biomaterial. Varying the FA treatment time led to different scaffold morphologies and resul…

ScaffoldTime FactorsFormatesBiocompatibilityBiomedical EngineeringNeovascularization PhysiologicMedicine (miscellaneous)FibroinConnective tissueRegenerative MedicineRegenerative medicineBiomaterialsTissue engineeringmedicineAnimalsRegenerationRats WistarStaining and LabelingTissue EngineeringTissue ScaffoldsChemistryBiomaterialHistologyRatsmedicine.anatomical_structureMicroscopy Electron ScanningFibroinsBiomedical engineeringJournal of Tissue Engineering and Regenerative Medicine
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Serotoninergic innervation of nonprincipal cells in the cerebral cortex of the lizard Podarcis hispanica.

2004

The mechanism of serotoninergic transmission in the neo- and archicortex of mammals kis complex, including both synaptic and nonsynaptic components, direct actions on principal cells, and indirect effects mediated by GABAergic interneurons. Here we studied the termination pattern and synaptic organization of the serotoninergic afferents in the cerebral cortex of the lizard, Podarcis hispanica, which is considered to correspond in part to the mammalian hippocampal formation, with the aim of unraveling basic, phylogenetically preserved rules in the connectivity of this pathway. We demonstrate that serotoninergic afferents, visualized by immunostaining for serotonin itself, establish multiple …

SerotoninHippocampal formationInhibitory postsynaptic potentialSerotonergicPodarcis hispanicaNerve FibersmedicineAnimalsNeuropeptide YTissue DistributionOpioid peptidegamma-Aminobutyric AcidCerebral CortexbiologyStaining and LabelingGeneral NeuroscienceLizardsbiology.organism_classificationMicroscopy Electronmedicine.anatomical_structureParvalbuminsCerebral cortexSynapsesbiology.proteinImmunologic TechniquesGABAergicEndorphinsNeuroscienceParvalbuminThe Journal of comparative neurology
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Electrophoretic analysis of heterogeneous lipopolysaccharides from various strains of Vibrio vulnificus biotypes 1 and 2 by silver staining and immun…

1992

Lipopolysaccharides (LPS) of 11 strains of Vibrio vulnificus biotypes 1 and 2, isolated from an eel farm, and of 10 reference strains, were examined by SDS-polyacrylamide gel electrophoresis coupled with silver staining and immunoblotting. LPS samples were obtained from whole-cell lysates, outer membrane fragments, and extracellular products. By silver staining, only a diffuse band of low-molecular weight could be visualized in all cases except for a biotype 1 strain isolated from water. However, immunoblotting with antisera obtained against strains of biotypes 1 and 2 from eels allowed visualization of multiple O-polysaccharide chains. All biotype 2 strains, independently of their origins,…

SerotypeLipopolysaccharidesSilver StainingBlotting WesternVibrio vulnificusApplied Microbiology and BiotechnologyMicrobiologyMicrobiologySilver stainSpecies SpecificityVibrionaceaeAgglutination TestsAnimalsVibrioGel electrophoresisAntiserumEelsbiologyPolysaccharides BacterialO AntigensGeneral Medicinebiology.organism_classificationMolecular biologyAntibodies BacterialElectrophoresis Polyacrylamide GelRabbitsBacterial outer membraneBacteriaCurrent microbiology
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Comparison of the exoproducts of gram-negative bacteria by SDS-page

1985

The protein exoproducts released during exponential growth of Gram-negative bacteria were analysed and compared by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-Page). The following bacterial strains were tested: Escherichia coli, Klebsiella pneumoniae, Citrobacter freundii, Enterobacter cloacae, Serratia liquefaciens, Serratia rubidaea, Proteus mirabilis, Proteus vulgaris, Salmonella minnesota, Pseudomonas aeruginosa and Pseudomonas fluorescens. It is demonstrated by SDS-Page that members of one species show identical protein pattern, whereas different species show besides comparable protein bands a species characteristic pattern. All members of Enterobacteriaceae were sho…

SilverStaining and LabelingbiologyImmunologyPseudomonasProteus vulgarisPseudomonas fluorescensUrinebiology.organism_classificationSerratia liquefaciensProteus mirabilisEnterobacteriaceaeMicrobiologyCitrobacter freundiiMolecular WeightBacterial ProteinsEnterobacteriaceaeSpecies SpecificityBiochemistryGram-Negative BacteriaHumansElectrophoresis Polyacrylamide GelSulfhydryl CompoundsPeptidesEnterobacter cloacaeZentralblatt für Bakteriologie, Mikrobiologie und Hygiene. Series A: Medical Microbiology, Infectious Diseases, Virology, Parasitology
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3D Morphology, ultrastructure and development of Ceratomyxa puntazzi stages: first insights into the mechanisms of motility and budding in the Myxozo…

2012

Free, amoeboid movement of organisms within media as well as substrate-dependent cellular crawling processes of cells and organisms require an actin cytoskeleton. This system is also involved in the cytokinetic processes of all eukaryotic cells. Myxozoan parasites are known for the disease they cause in economical important fishes. Usually, their pathology is related to rapid proliferation in the host. However, the sequences of their development are still poorly understood, especially with regard to pre-sporogonic proliferation mechanisms. The present work employs light microscopy (LM), electron microscopy (SEM, TEM) and confocal laser scanning microscopy (CLSM) in combination with specific…

SporesIndolesPhalloidineParasitic Diseases AnimalBiophysicsMotilitylcsh:MedicineBiologyBiochemistryFish DiseasesMicroscopy Electron TransmissionCell MovementMolecular Cell BiologyOxazinesAnimalsBilePseudopodiaMyxozoaCytoskeletonlcsh:ScienceBiologyCell ProliferationAmoeboid movementBuddingLife Cycle StagesMultidisciplinaryMicroscopy ConfocalStaining and LabelingPhysicslcsh:RProteinsCell BiologyActin cytoskeletonCellular StructuresSea BreamCell biologyUltrastructureMicroscopy Electron Scanninglcsh:QFilopodiaZoologyCytokinesisCell DivisionResearch ArticleDevelopmental BiologyPLoS ONE
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