Search results for "Immunochemistry"

showing 8 items of 28 documents

Immunochemical faecal occult blood tests for colorectal cancer screening: No time to lose

2013

Malemedicine.medical_specialtyHepatologybusiness.industryImmunochemistryGastroenterologyFaecal occult bloodGastroenterologyColorectal cancer screeningOccult BloodInternal medicineImmunochemistryHumansMedicineFemaleColorectal NeoplasmsbusinessDigestive and Liver Disease
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Expression and inducibility of drug-metabolizing enzymes in preneoplastic and neoplastic lesions of rat liver during nitrosamine-induced hepatocarcin…

1987

The expression, inducibility, and regulation of four different cytochrome (cyt.) P-450 isoenzymes (PB1, PB2, MC1, and MC2) NADPH-cytochrome P-450 reductase, the glutathione transferases (GSTs) B and C and microsomal epoxide hydrolase (mEHb) have been studied during nitrosamine-induced hepatocarcinogenesis using immunohistochemical techniques. The investigations revealed basic differences in the expression of the individual drug metabolizing enzymes in the course of neoplastic development. While the two GSTs and mEHb were increased in all preneoplastic and benign neoplastic lesions, the levels of the distinct cyt. P-450 isoenzymes were characteristically different from each other. Following …

NitrosaminesCytochromeHealth Toxicology and MutagenesisReductaseToxicologyenvironment and public healthIsozymeMixed Function Oxygenaseschemistry.chemical_compoundLiver Neoplasms ExperimentalCytochrome P-450 Enzyme SystemAnimalsCytochrome P-450 Enzyme InhibitorsAdenosine Triphosphataseschemistry.chemical_classificationbiologyHistocytochemistryImmunochemistryProteinsRats Inbred StrainsGeneral MedicineMolecular biologyRatsenzymes and coenzymes (carbohydrates)Drug metabolizing enzymesEnzymeLiverchemistryBiochemistryNitrosamineEnzyme InductionMicrosomal epoxide hydrolaseembryonic structurescardiovascular systembiology.proteinImmunohistochemistryFemalePrecancerous ConditionsArchives of Toxicology
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Improving uptake of screening for colorectal cancer: a study on invitation strategies and different test kit use

2015

Objective The aim of this study was to compare the uptake of mail-delivered tests for colorectal cancer screening. We assessed the effect of an advance notification letter and a reminder letter, and analysed the proportion of inappropriately handled tests. Materials and methods Fifteen thousand randomly selected residents of Latvia aged 50–74 years were allocated to receive one of three different test systems: either a guaiac faecal occult blood test (gFOBT) or one of two laboratory-based immunochemical tests (FIT) – FOB Gold or OC-Sensor. Half of the target population received an advance notification letter; all nonresponders were sent a reminder letter. Results The uptake of screening was…

OncologyMalemedicine.medical_specialtygenetic structuresColorectal cancerReminder Systemseducationcolorectal cancer screeningfaecal occult blood testSpecimen HandlingRandom AllocationInternal medicinemedicinePostal serviceOriginal Articles: Colorectal CancerHumansPostal ServiceEarly Detection of CancerAgedRandom allocationGynecologyHepatologybusiness.industryImmunochemistryGastroenterologyMiddle AgedPatient Acceptance of Health Caremedicine.diseasefaecal immunochemical testCorrespondence as TopicLatviaadvance notification letterTest (assessment)Colorectal cancer screeninguptakeOccult BloodFemaleFaecal occult blood testbusinessColorectal NeoplasmsGuaiacEuropean Journal of Gastroenterology & Hepatology
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6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase from frog skeletal muscle: purification, kinetics and immunological properties.

1993

Fructose 2,6-bisphosphate is the most potent activator of 6-phosphofructo-1-kinase, a key regulatory enzyme of glycolysis in animal tissues. This study was prompted by the finding that the content of fructose 2,6-bisphosphate in frog skeletal muscle was dramatically increased at the initiation of exercise and was closely correlated with the glycolytic flux during exercise. 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase, the enzyme system catalyzing the synthesis and degradation of fructose 2,6-bisphosphate, was purified from frog (Rana esculenta) skeletal muscle and its properties were compared with those of the rat muscle type enzyme expressed in Escherichia coli using recombinant DN…

PhysiologyPhosphofructokinase-2BiologyBiochemistrychemistry.chemical_compoundEndocrinologymedicineFructosediphosphatesAnimalsGlycolysisPhosphorylationEcology Evolution Behavior and Systematicschemistry.chemical_classificationMolecular massImmunochemistryMusclesPhosphotransferasesSkeletal muscleRana esculentaFructoseHydrogen-Ion ConcentrationMolecular WeightKineticsmedicine.anatomical_structureEnzymechemistryFructose 26-bisphosphateBiochemistryGRENOUILLEAnimal Science and ZoologyPhosphoenolpyruvate carboxykinaseProtein KinasesJournal of comparative physiology. B, Biochemical, systemic, and environmental physiology
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Absence Ochratoxin A in soy sauce

2004

A method is described for the determination of ochratoxin A (OTA) in soy sauce using phosphate-buffered saline (PBS) extraction, an immunoaffinity clean-up, a liquid chromatographic determination with fluorescence detection (LC-FD) and confirmation with LC-FD after methylation of OTA. Recoveries of OTA spiked to soy sauce samples at 0.25 ng/ml level were 90% with relative standard deviations of 4%. The limit of detection was 0.01 ng/ml for OTA using the proposed method. Furthermore, the proposed method was applied to 60 soy sauce samples from China and Japan and none of them were found to contain OTA.

Quality ControlOchratoxin ADetection limitChromatographyImmunochemistryExtraction (chemistry)Soy FoodsFood ContaminationGeneral MedicineOchratoxinsSensitivity and SpecificityMicrobiologyFluorescencechemistry.chemical_compoundchemistryFood scienceChromatography LiquidFood ScienceInternational Journal of Food Microbiology
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The (2'-5')Oligoadenylate Synthetase is Present in the Lowest Multicellular Organisms, the Marine Sponges. Demonstration of the Existence and Identif…

1995

We have proved the presence of (2'-5')oligoadenylates [(2'-5')An] and oligoadenylate synthetase [(2'-5')An synthetase] in the marine sponge Geodia cydonium. (2'-5')An isolated from sponge crude extract competed with authentic (2'-5')An for binding to polyclonal antiserum against (2'-5')An. HPLC analysis revealed the presence of nucleotides eluting with molecular markers for (2'-5')A oligomers. The biological activity of sponge (2'-5')An was demonstrated by inhibiting the protein biosynthesis in rabbit reticulocyte lysate. The activity of the (2'-5')An synthetase, present in crude sponge extract, was found to be high compared to that in mammalian interferon-treated cell extract. The (2'-5')A…

ReticulocytesBlotting WesternCross ReactionsIn Vitro TechniquesBiochemistrylaw.inventionMiceSpecies SpecificityWestern blotlawAdenine nucleotide2'5'-Oligoadenylate SynthetasemedicineAnimalsChromatography High Pressure LiquidProtein Synthesis InhibitorsAntiserumchemistry.chemical_classificationOligoribonucleotidesbiologymedicine.diagnostic_testAdenine Nucleotides2'-5'-OligoadenylateImmunochemistryBlood Proteinsbiology.organism_classificationBiological EvolutionMolecular biologyPoriferaRatsMolecular WeightSpongeEnzymeBiochemistrychemistryPolyclonal antibodiesbiology.proteinRecombinant DNARabbitsEuropean Journal of Biochemistry
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Inhibition of in vitro reconstitution of rotavirus transcriptionally active particles by anti-VP6 monoclonal antibodies

1994

International audience; Six monoclonal antibodies specific for the major capsid protein of rotavirus, VP6, previously characterized, were tested in a biological assay for their capacity to block the transcriptase activity associated with the single-shelled particles. The results showed that two MAbs (RV-50 and RV-133), specific for distinct antigenic sites, were able to block the transcription when they were incubated with a purified baculovirus-expressed group A VP6, prior to the reconstitution of the single-shelled particles from the cores, suggesting that at least two domains are involved in active single-shelled particle reconstitution. The results obtained previously from immunochemist…

RotavirusTranscription Geneticmedicine.drug_classvirusesBiologyMothsMonoclonal antibodymedicine.disease_causeTransfectionAntiviral AgentsCell Line03 medical and health sciencesCapsidAntigenTranscription (biology)VirologyRotavirusImmunochemistrymedicineAnimalsRNA MessengerAntigens Viral030304 developmental biology0303 health sciences030306 microbiologyAntibodies MonoclonalBiological activityRNA-Directed DNA PolymeraseGeneral MedicineDNA-Directed RNA PolymerasesBIOLOGIE MOLECULAIREChromatography Ion ExchangeVirologyMolecular biologyIn vitro3. Good healthVIROLOGIECapsid[SDV.MP.VIR]Life Sciences [q-bio]/Microbiology and Parasitology/VirologyChromatography GelCapsid ProteinsBaculoviridae
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Antigenic cell wall mannoproteins in Candida albicans isolates and in other Candida species.

1991

Polyclonal antibodies (pAbs) and monoclonal antibodies (mAbs), raised against mannoprotein components from Candida albicans ATCC 26555 (serotype A) blastoconidia and mycelial cell walls, were used to investigate antigenic similarities among wall mannoproteins from other C. albicans serotype A and B strains, and from C. tropicalis and C. guilliermondii. Radioactively labelled walls isolated from cells grown at either 28 degrees C or 37 degrees C were digested with a beta-glucanase complex (Zymolyase 20T) to release cell-wall-bound mannoproteins. Numerous molecular species with different electrophoretic mobilities were released from the various isolates. Differences appeared to be related to …

SerotypeAntigenicityAntigens FungalHydrolasesMicrobiologyBlastoconidiumMicrobiologyCell wallFungal ProteinsEpitopesSpecies SpecificityCell WallCandida albicansCandida albicansCandidaMembrane GlycoproteinsMolecular massbiologyImmunochemistryAntibodies MonoclonalMembrane Proteinsbiology.organism_classificationCorpus albicanscarbohydrates (lipids)BiochemistrySolubilityPolyclonal antibodiesbiology.proteinJournal of general microbiology
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