Search results for "Affinity"

showing 10 items of 313 documents

Isolation and characterization of maerophage-derived C1q and its similarities to serum C1q

1986

Recently, we have shown that the collagen-like, Fc-recognizing subcomponent C1q of the first complement component is synthesized by human, guinea pig and mouse peritoneal macrophages. To test whether macrophages may contribute to the serum pool of C1q, C1q was purified from guinea pig serum and from guinea pig peritoneal macrophage supernatants and compared for similarities. Both molecules had a similar sedimentation rate (macrophage C1q: 11.3 S, serum C1q: 11.2 S) and showed on sodium dodecyl sulfate-polyacrylamide gel electrophoresis under reducing conditions three identical bands with molecular weights of Mr, 29 000, Mr, 27 000 and Mr 23 000 for the A, B and C chains, respectively. Both …

MaleComplement Activating EnzymesGuinea PigsImmunologychemical and pharmacologic phenomenaImmunoelectrophoresisBiologyurologic and male genital diseasesChromatography AffinityGuinea pigfluids and secretionsAntigenimmune system diseasesmedicineAnimalsImmunology and AllergyMacrophageskin and connective tissue diseasesComplement C1qGel electrophoresisMolecular massmedicine.diagnostic_testComplement C1qMacrophagesOuchterlony double immunodiffusionBiochemistryFemaleEuropean Journal of Immunology
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Clozapine: Strong antiaggressive effects with minimal motor impairment

1992

Abstract Clinical studies have shown clozapine to be effective in the treatment of schizophrenia and associated with an extremely low incidence of extrapiramidal side effects. Diverse studies indicate that clozapine is an atypical neuroleptic with a preferential activity on the mesolimbic structures and a lower affinity for striatal D2 receptors than the classical antipsychotics. The purpose of this study was to assess the behavioral properties of clozapine, especially its effects on aggressive and motor behaviors. Individually housed male mice of the OF1 strain were exposed to anosmic “standard opponents” 30 minutes after the last drug administration. One category of animals received a sin…

MaleMale miceExperimental and Cognitive PsychologyAtypical neurolepticMotor ActivityPharmacologyMiceBehavioral NeuroscienceDopamine receptor D2medicineAnimalsClozapineClozapineDose-Response Relationship DrugDrug administrationMotor impairmentmedicine.diseaseAggressionLower affinityMotor SkillsSchizophreniaAnesthesiaArousalPsychologyPsychomotor Performancemedicine.drugPhysiology & Behavior
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Rapid mycotoxin analysis in human urine: A pilot study

2011

A simple and rapid method effective for quantitative determination of deoxynivalenol (DON), T-2 toxin (T-2), HT-2 toxin (HT-2), zearalenone (ZEN), ochratoxin A (OTA), aflatoxins (AFs) B(1), B(2), G(1) and G(2) and fumonisins FB(1) and FB(2) in urine was developed. The urine was diluted with phosphate buffer solution (PBS) and thoroughly mixed. For clean-up and extraction, the mixture was loaded on a MYCO 6in1 IAC. Hybrid triple quadrupole-linear ion trap mass spectrometer (QTrap) was used for the detection. Extra tools for confirmation of selected mycotoxins in positive samples, Information Dependent Acquisition (IDA) experiments, were also developed. The use of immunoaffinity columns follo…

MaleOchratoxin AAflatoxinIAC columnsPilot ProjectsUrineUrineToxicologyTandem mass spectrometryChromatography Affinitychemistry.chemical_compoundLimit of DetectionTandem Mass SpectrometryHumansMycotoxinZearalenoneDetection limitChromatographyChemistryExtraction (chemistry)Reproducibility of ResultsGeneral MedicineMycotoxinsReference StandardsFemaleQTrapFood ScienceFood and Chemical Toxicology
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Identification and purification of a stress associated nuclear carbohydrate binding protein (Mr 33000) from rat liver by application of a new photore…

1994

A photoreactive alpha-D-glucose probe has been designed for the specific detection of carbohydrate binding proteins (CBPs). The probe consists of four parts: (i) an alpha-D-glucose moiety; (ii) the digoxigenin tag; (iii) the photoreactive cross-linker; and (iv) the lysyl-lysine backbone. After incubation with lectins in the dark, the probe is activated and cross-linked to the CBPs after being treated by several flashes. Using this method we have identified a new alpha-D-glucose CBP of M(r) = 33,000, termed CBP33, in the nuclei of rats exposed to transient immobilization stress. Monoclonal antibodies were raised against the partially purified protein and subsequently used to enrich CBP33. It…

MalePhotochemistrymedicine.drug_classMolecular Sequence DataReceptors Cell SurfaceAsialoglycoprotein ReceptorMonoclonal antibodyBiochemistryChromatography Affinitychemistry.chemical_compoundAffinity chromatographyStress PhysiologicalLectinsmedicineAnimalsMoietyDigoxigeninAmino Acid SequenceRats WistarCarbohydrate-responsive element-binding proteinMolecular BiologyCell NucleusChromatographyLysineCarbohydrate-binding proteinCell BiologyCarbohydrateRatsCross-Linking ReagentsGlucoseLiverchemistryBiochemistryMolecular ProbesRat liverElectrophoresis Polyacrylamide GelDigoxigeninGlycoconjugate Journal
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Association of a polyuridylate-specific endoribonuclease with small nuclear ribonucleo-proteins which had been isolated by affinity chromatography us…

1983

Immunoglobulins, containing antibodies against U1-snRNP, have been prepared from a patient with systemic lupus erythematosus. After coupling these antibodies to a Sepharose matrix, U-snRNPs have been isolated and purified from rat liver nuclei by use of immunoaffinity chromatography. The resulting RNPs had the typical protein pattern of U-sn RNPs and a sedimentation coefficient of 12 S. The U-snRNP preparation was associated with an endoribonuclease which required Mg2+ for optimal activity. The enzyme, with an pH optimum of 6.2, degraded only poly(U). Other single-stranded polyribo- and polydeoxyribonucleotides, tRNA, as well as double-stranded RNA and DNA were not digested. The products of…

MalePoly UEndoribonucleaseAntibody AffinityBiologyenvironment and public healthBiochemistryChromatography AffinitySubstrate SpecificitySepharosechemistry.chemical_compoundAffinity chromatographyEndoribonucleasesAnimalsHumansLupus Erythematosus Systemicchemistry.chemical_classificationImmunochemistryRNARats Inbred StrainsRibonucleoproteins Small NuclearMolecular biologyRatsEnzymechemistryLiverRibonucleoproteinsAntibodies AntinuclearImmunoglobulin GRNA splicingTransfer RNADNAEuropean journal of biochemistry
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Proneurotrophin Binding to P75 Neurotrophin Receptor (P75ntr) Is Essential for Brain Lesion Formation and Functional Impairment after Experimental Tr…

2015

Traumatic brain injury (TBI) initiates an excessive mediator release of e.g. neurotrophins, which promote neuronal survival, differentiation, and modulate synaptic plasticity. Paradoxically, mature forms of neurotrophins promote neuronal survival, whereas unprocessed forms of neurotrophins induce cell death through p75 neurotrophin receptor (p75NTR) signaling. p75NTR is widely expressed during synaptogenesis and is subsequently downregulated in adulthood. Repair mechanisms after acute cerebral insults can reactivate its expression. Therefore, the influence of p75NTR on secondary brain damage was addressed. mRNA levels of p75NTR and its ligands were quantified in brain tissue up to 7 days af…

MaleProgrammed cell deathmedicine.medical_specialtyTraumatic brain injurySynaptogenesisReceptors Nerve Growth FactorBrain damageMiceInternal medicineAnimalsMedicineLow-affinity nerve growth factor receptorRNA MessengerMice KnockoutBehavior AnimalCell Deathbiologybusiness.industrymedicine.diseaseMice Inbred C57BLDisease Models AnimalEndocrinologyBrain InjuriesSynaptic plasticitybiology.proteinFemalesense organsNeurology (clinical)medicine.symptomSignal transductionbusinessNeuroscienceProtein BindingSignal TransductionNeurotrophinJournal of Neurotrauma
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Characterization of rat glutathione transferases in olfactory epithelium and mucus

2019

International audience; The olfactory epithelium is continuously exposed to exogenous chemicals, including odorants. During the past decade, the enzymes surrounding the olfactory receptors have been shown to make an important contribution to the process of olfaction. Mammalian xenobiotic metabolizing enzymes, such as cytochrome P450, esterases and glutathione transferases (GSTs), have been shown to participate in odorant clearance from the olfactory receptor environment, consequently contributing to the maintenance of sensitivity toward odorants. GSTs have previously been shown to be involved in numerous physiological processes, including detoxification, steroid hormone biosynthesis, and am…

MaleProteomicsPhysiologyScienceMaterials ScienceEnzyme MetabolismRespiratory SystemResearch and Analysis MethodsBiochemistryOlfactory Receptor NeuronsOlfactory Mucosa[SDV.BBM] Life Sciences [q-bio]/Biochemistry Molecular BiologyMedicine and Health SciencesGlutathione ChromatographyAnimals[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular BiologyAmino Acid SequenceRats Wistar[SDV.MHEP.OS]Life Sciences [q-bio]/Human health and pathology/Sensory OrgansEnzyme ChemistryMaterialsImmunohistochemistry TechniquesGlutathione TransferaseAffinity ChromatographyChromatographic TechniquesQRBiology and Life SciencesProteinsGlutathioneImmunohistochemistryBody FluidsEnzymesRatsHistochemistry and Cytochemistry TechniquesMucusNasal Mucosa[SDV.MHEP.OS] Life Sciences [q-bio]/Human health and pathology/Sensory OrgansAmino Acid Specific ChromatographyPhysical SciencesOdorantsEnzymologyImmunologic TechniquesMedicineAnatomyPeptidesResearch Article
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The major isozyme of rat cardiac glutathione transferases. Its correspondence to hepatic transferase X.

1986

1. A major isozyme of rat heart glutathione transferase was purified to homogeneity by Sephadex G-200 gel filtration, ammonium sulfate precipitation, CM-cellulose chromatography and affinity chromatography on S-hexylglutathione-linked Sepharose 6B. 2. The purified isozyme was a dimer with an apparent relative molecular mass of 50000 composed of two Yb-size subunits (Mr= 26 500). The isozyme is immunologically related to rat liver glutathione transferase X and 3–3, especially closely to transferase X, and no immunological cross-reactivity with subunits 1 and 2 of hepatic glutathione transferases was observed. The isoelectric point (pI = 6.9) of the isozyme was identical with and the substrat…

MalePyruvate dehydrogenase lipoamide kinase isozyme 1ImmunodiffusionBiologyBiochemistryIsozymeChromatography AffinitySubstrate SpecificitySepharosechemistry.chemical_compoundAffinity chromatographyTransferaseAnimalsIsoelectric PointGlutathione TransferaseMolecular massMyocardiumRats Inbred StrainsGlutathioneHydrogen-Ion ConcentrationMolecular biologyRatsIsoenzymesMolecular WeightIsoelectric pointchemistryBiochemistryLiverChromatography GelElectrophoresis Polyacrylamide GelEuropean journal of biochemistry
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In vitro modeling of the ternary interaction in juvenile hormone metabolism

1996

The gradual decline in juvenile hormone (JH) titer followed by its complete clearance early in the last larval instar is required for the onset of the metamorphosis of lepidopterous larvae. JH titer is regulated by both biosynthesis and degradation. Two major pathways for JH metabolism, ester hydrolysis and epoxide hydration, are due to JH esterase (JHE) and JH epoxide hydrolase (JHEH), respectively. In vitro experiments designed to elucidate the molecular mechanism of JH metabolism are described. First, microsomal JHEH in Manduca sexta eggs was identified by using photoaffinity analogs of JH, and purified to homogeneity with ion exchange and hydroxylapatite columns. Purified JHEH from M. s…

Manduca sextaJH binding proteinJH epoxide hydrolaseJH esterasephotoaffinity labelingArchives of Insect Biochemistry and Physiology
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Purification and reassessment of ligand binding by the recombinant, putative juvenile hormone receptor of the tobacco hornworm, Manduca sexta

1996

The 29 kDa protein from the larval epidermis of the tobacco hornworm, Manduca sexta, that specifically bound photoaffinity analogs of JH I and JH II was produced by a recombinant baculovirus (rJP29). The higher of the two molecular weight forms made corresponded to a protein that could be formed by read‐through of the TGA termination codon to the following TAA. The previously reported, apparent high affinity binding of [methyl‐3H]‐JH I by rJP29 as measured by the dextran‐coated charcoal (DCC) assay [Palli et al., Proc Natl Acad Sci USA 91:6191–6195 (1994)] was found to be artifactual due to endogenous cellular esterases that co‐purified with rJP29 through both DEAE cellulose and MonoQ chrom…

Manduca sextaTn5 cellsjuvenile hormone receptorcellular esterasesSf21 cellsrecombinant baculovirus proteinJH esterasephotoaffinity labelingArchives of Insect Biochemistry and Physiology
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