Search results for "Assay"

showing 10 items of 2241 documents

Design, synthesis, and biological evaluation of thiophene analogues of chalcones.

2008

Chalcones are characterized by possessing an enone moiety between two aromatic rings. A series of chalcone-like agents, in which the double bond of the enone system is embedded within a thiophene ring, were synthesized and evaluated for antiproliferative activity and inhibition of tubulin assembly and colchicine binding to tubulin. The replacement of the double bond with a thiophene maintains antiproliferative activity and therefore must not significantly alter the relative conformation of the two aryl rings. The synthesized compounds were found to inhibit the growth of several cancer cell lines at nanomolar to low micromolar concentrations. In general, all compounds having significant anti…

G2 PhaseModels MolecularDouble bondStereochemistryClinical BiochemistryPharmaceutical ScienceEtherAntineoplastic Agentsmacromolecular substancesThiophenesBiochemistryChemical synthesischemistry.chemical_compoundMiceStructure-Activity RelationshipChalconesTubulinCell Line TumorDrug DiscoveryThiopheneMoietyAnimalsHumansMolecular BiologyCell Proliferationchemistry.chemical_classificationBinding SitesbiologyDose-Response Relationship DrugMolecular StructureArylOrganic ChemistryCell CycleBrainStereoisomerismTubulin ModulatorsTubulinchemistryDrug Designbiology.proteinMolecular MedicineCattleDrug Screening Assays AntitumorColchicineK562 CellsEnoneCell DivisionHeLa CellsBioorganicmedicinal chemistry
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Curcumin and trans-resveratrol exert cell cycle-dependent radioprotective or radiosensitizing effects as elucidated by the PCC and G2-assay

2013

Curcumin and trans-resveratrol are well-known antioxidant polyphenols with radiomodulatory properties, radioprotecting non-cancerous cells while radiosensitizing tumor cells. This dual action may be the result of their radical scavenging properties and their effects on cell-cycle checkpoints that are activated in response to radiation-induced chromosomal damage. It could be also caused by their effect on regulatory pathways with impact on detoxification enzymes, the up-regulation of endogenous protective systems, and cell-cycle-dependent processes of DNA damage. This work aims to elucidate the mechanisms underlying the dual action of these polyphenols and investigates under which conditions…

G2 PhaseRadiation-Sensitizing AgentsRadiosensitizerCurcuminAntioxidantDNA damageHealth Toxicology and Mutagenesismedicine.medical_treatmentRadioprotectorCellRadiation-Protective AgentsCHO CellsBiologyRadiation ToleranceCell Fusionchemistry.chemical_compoundCricetulusCricetinaeStilbenesGeneticsmedicineAnimalsHumansRadiosensitivityMolecular BiologyCells CulturedMutagenicity TestsCell CycleCell cycleChromatin Assembly and DisassemblyRadiosensitizermedicine.anatomical_structureG2-assayBiochemistrychemistryResveratrolPeripheral blood lymphocyteCancer researchCurcumintrans-ResveratrolPremature chromosome condensationMutation Research/Fundamental and Molecular Mechanisms of Mutagenesis
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GIV noroviruses and other enteric viruses in bivalves: a preliminary study.

2012

We evaluated the presence of the enteric viruses: norovirus, adenovirus, enterovirus, astrovirus, hepatitis A virus, and hepatitis E virus in bivalves using nested PCR methods and cell culture assays. Noroviruses GII.4 and GIV.1, adenoviruses types 1 and 2, hepatitis A, and echovirus type 7 were detected in the shellfish tested, which were often co-infected. This is the first study to detect such a high level of viral contamination in Italian mussels (up to four different viral groups in a single sample), and the first to document the presence of GIV NoV in shellfish.

GIV noroviruMicrobiology (medical)PCR assayEnteric viruseEnteric viruses; GIV norovirus; PCR assays; Shellfish; Microbiology (medical)Shellfish
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Binding and/or hydrolysis of purine‐based nucleotides is not required for IM30 ring formation

2021

IM30, the inner membrane-associated protein of 30 kDa, is conserved in cyanobacteria and chloroplasts. Although its exact physiological function is still mysterious, IM30 is clearly essential for thylakoid membrane biogenesis and/or dynamics. Recently, a cryptic IM30 GTPase activity has been reported, albeit thus far no physiological function has been attributed to this. Yet, it is still possible that GTP binding/hydrolysis affects formation of the prototypical large homo-oligomeric IM30 ring and rod structures. Here, we show that the Synechocystis sp. PCC 6803 IM30 protein in fact is an NTPase that hydrolyzes GTP and ATP, but not CTP or UTP, with about identical rates. While IM30 forms lar…

GTP'Genetic VectorsBiophysicsGene ExpressionGTPaseRing (chemistry)ThylakoidsBiochemistrySubstrate Specificity03 medical and health sciencesAdenosine TriphosphateBacterial ProteinsStructural BiologyEscherichia coliGeneticsNucleotideddc:610Cloning MolecularMolecular BiologyEnzyme Assays030304 developmental biologychemistry.chemical_classification0303 health sciencesbiologyChemistryHydrolysis030302 biochemistry & molecular biologySynechocystisSynechocystisMembrane ProteinsCell BiologyNucleoside-Triphosphatasebiology.organism_classificationRecombinant ProteinsKineticsMicroscopy ElectronThylakoidMembrane biogenesisBiophysicsGuanosine TriphosphateBiogenesisProtein BindingFEBS Letters
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Comparative analysis of DNA breakage, chromosomal aberrations and apoptosis induced by the anti-herpes purine nucleoside analogues aciclovir, gancicl…

2002

Nucleoside analogues have been used in antiviral therapy and suicide cancer gene therapy. Therefore, it is of importance to compare their potential cytotoxic and genotoxic action. Using metabolically competent CHO cells expressing the thymidine kinase gene of herpes simplex virus type 1 (CHO-HSVtk cells) as a model system, the induction of DNA breaks was compared with the induction of structural chromosomal aberrations and apoptosis/necrosis after exposure to the anti-herpes nucleoside analogues aciclovir (ACV), ganciclovir (GCV) and penciclovir (PCV). After continuous treatment of CHO-HSVtk cells with the drugs, LD(10) in a colony-forming assay was 50, 0.5 and 1 microM for ACV, GCV and PCV…

GanciclovirGuanineDNA damagevirusesHealth Toxicology and MutagenesisAcyclovirApoptosisCHO CellsBiologymedicine.disease_causeAntiviral AgentsThymidine KinaseChromosomesColony-Forming Units AssayNecrosisCricetulusCricetinaeGeneticsmedicineCytotoxic T cellAnimalsSimplexvirusAciclovirEnzyme InhibitorsMolecular BiologyGanciclovirChromosome AberrationsDNAMolecular biologyHerpes simplex virusApoptosisPenciclovirNucleosidemedicine.drugDNA DamageMutation research
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Efficient Extraction of Olive Pulp and Stone Proteins by using an Enzyme-Assisted Method

2014

An efficient protein extraction protocol for proteins from olive pulp and stone by using enzymes was developed. For this purpose, different parameters that affect the extraction process, such as enzyme type and content, pH, and extraction temperature and time, were tested. The influence of these factors on protein recovery was examined using the standard Bradford assay, while the extracted proteins were characterized by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE). The best extraction conditions were achieved at pH 7.0 and 5% (v/v) Palatase® 20000 L (lipase) for pulp and Lecitase® Ultra (phospholipase) for stone proteins. The optimal extraction temperature and time w…

Gel electrophoresisChromatographybiologyChemistryPulp (paper)Extraction (chemistry)engineering.materialElectrophoresisProtein purificationengineeringbiology.proteinLipasePolyacrylamide gel electrophoresisBradford protein assayFood ScienceJournal of Food Science
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Sinusoidal endothelial cells from guinea pig liver synthesize and secrete cellular fibronectin in vitro.

1987

Endothelial liver cells were obtained from guinea pig by enzymatic digestion and centrifugal elutriation. Cells were cultured on gelatin and fibronectin pretreated culture vessels. Endothelial cells were characterized by phase-contrast microscopy, electron microscopy and the presence of Factor VIII-related antigen. Fibronectin secretion was determined in cell-free supernatants by a sensitive and specific ELISA and localized on fixed cultured cells by immunofluorescence. [35S]Methionine endogeneously labeled fibronectin was immunoprecipitated from supernatants and cellular lysates and displayed on sodium dodecyl sulfate polyacrylamide slab gel electrophoresis. After attachment to the culture…

Gel electrophoresisHepatologymedicine.diagnostic_testbiologyGuinea PigsFluorescent Antibody TechniqueEnzyme-Linked Immunosorbent AssayImmunofluorescenceMolecular biologyIn vitroFibronectinsFibronectinEndothelial stem cellPerisinusoidal spacemedicine.anatomical_structureLiverCell cultureHepatocytemedicinebiology.proteinAnimalsElectrophoresis Polyacrylamide GelFemaleEndotheliumCells CulturedHepatology (Baltimore, Md.)
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Semi-automatic quantitative RT-PCR to measure CYP induction by drugs in human hepatocytes

2003

An assay has been developed for the quantitative measurement of CYP mRNA content of the major human isoforms (1A1, 1A2, 2A6, 2B6, 2C9, 2C19, 2D6, 2E1, 3A4 and 3A5) in human hepatocytes. The method is based on the conversion of mRNAs into their corresponding cDNAs, followed by PCR amplification using appropriate primers. Making use of appropriate internal and external standards it is possible to estimate changes in CYP mRNA content of hepatocytes. The technique has been standardised to run semi-automatically. This procedure can be used to assess the CYP induction potential of new pharmaceuticals at a pre-clinical stage of development. To this aim, human hepatocytes obtained from functional l…

Gene isoformMessenger RNADrug-Related Side Effects and Adverse ReactionsbiologyReverse Transcriptase Polymerase Chain ReactionDrug Evaluation PreclinicalCytochrome P450General MedicineToxicologyIsozymeMolecular biologyReverse transcriptaseXenobioticsReverse transcription polymerase chain reactionReal-time polymerase chain reactionCytochrome P-450 Enzyme SystemBiochemistryEnzyme InductionComplementary DNAHepatocytesbiology.proteinHumansBiological AssayRNA MessengerCells CulturedToxicology in Vitro
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Application of an ectopic expression system for the selection of protein-isoform-specific antibodies. The monoclonal antibody K1 C3 is specific for t…

1993

Monoclonal antibodies were raised against a fusion protein consisting of a fragment of 141 amino acids of the C-terminal region of the rat brain voltage-gated K(+)-channel protein (RCK1) and the lambda N protein (fusion protein I). Selection of K(+)-channel-specific hybridoma cell lines was performed by means of an ELISA employing a fusion protein consisting of the K(+)-channel-specific peptide sequence and glutathione S-transferase (fusion protein II). For final selection of RCK1 isoform-specific antibodies, a panel of Xenopus oocytes was employed, each injected with cRNA coding for a specific RCK isoform (RCK 1, 2, 4 or 5). Several days after injection, cryosections of embedded oocytes we…

Gene isoformProtein isoformPotassium Channelsmedicine.drug_classBlotting WesternMolecular Sequence DataEnzyme-Linked Immunosorbent AssayMonoclonal antibodyBiochemistryMiceAntibody SpecificityProtein A/GTumor Cells CulturedmedicineAnimalsAmino Acid SequenceRats WistarPeptide sequenceBrain ChemistryMice Inbred BALB CHybridomasSequence Homology Amino AcidbiologyAntibodies MonoclonalFusion proteinMolecular biologyRatsBiochemistryPotassium Channels Voltage-Gatedbiology.proteinImmunohistochemistryAntibodyKv1.1 Potassium ChannelEuropean Journal of Biochemistry
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Influence of muscle strength and total work on exercise-induced plasma growth hormone isoforms in women

2003

The purpose of this investigation was to determine the influence of physical strength and the ability to do more total work on human growth hormone (GH) variants to a heavy resistance exercise protocol in untrained women. From a distribution of 100 healthy, untrained women, the strongest 10 women (S) and the weakest 10 women (W) were compared for GH responses pre- and post an acute heavy resistance exercise test (AHRET, 6 sets of 10 RM squats, 2 minutes rest between sets). Blood samples were obtained pre-exercise and immediately post-exercise and subsequently analysed in total as well as fractionated by Sephacryl S-100R column chromatography into three molecular weight size classes: fractio…

Gene isoformmedicine.medical_specialtyTotal workWeight LiftingPhysical Therapy Sports Therapy and RehabilitationFraction (chemistry)Physical strengthRats Sprague-DawleyPlasma growth hormoneInternal medicinemedicineAnimalsHumansProtein IsoformsBioassayOrthopedics and Sports MedicineExercise physiologyMuscle SkeletalExerciseTibiaChemistryRatsEndocrinologyGrowth HormonePhysical EnduranceBiological AssayFemaleMass fractionJournal of Science and Medicine in Sport
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