Search results for "Antiserum"

showing 10 items of 45 documents

LKM-1 autoantibodies recognize a short linear sequence in P450IID6, a cytochrome P-450 monooxygenase.

1991

LKM-1 autoantibodies, which are associated with autoimmune chronic active hepatitis, recognize P450IID6, a cytochrome P-450 monooxygenase. The reactivities of 26 LKM-1 antisera were tested with a panel of deletion mutants of P450IID6 expressed in Escherichia coli. 22 sera recognize a 33-amino acid segment of P450IID6, and 11 of these recognize a shorter segment, DPAQPPRD. PAQPPR is also found in IE175 of herpes simplex virus type 1 (HSV-1). Antibodies for HSV-1 proteins were detected by ELISA in 17 of 20 LKM-1 sera tested. An immobilized, synthetic peptide, DPAQPPRDC, was used to purify LKM-1 antibodies. Affinity purified LKM-1 autoantibodies react on immunoblots with a protein in BHK cells…

AdultMaleAdolescentHepatitis C virusMolecular Sequence DataHepacivirusmedicine.disease_causeAntibodies ViralEpitopeAutoimmune DiseasesEpitopesViral ProteinsCytochrome P-450 Enzyme SystemmedicineHumansSimplexvirusAmino Acid SequencePeptide sequenceAutoantibodiesHepatitis ChronicAntiserumbiologyAutoantibodyGeneral MedicineMonooxygenaseMiddle AgedVirologyHerpes simplex virusbiology.proteinOxygenasesFemaleAntibodyResearch ArticleThe Journal of clinical investigation
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Overexpression of human homologs of the bacterial DnaJ chaperone in the synovial tissue of patients with rheumatoid arthritis

1999

Objective To study the expression of the chaperone family of J proteins in the synovial tissue of patients with rheumatoid arthritis (RA) or osteoarthritis. Methods Rabbit antibodies specific for a synthetic peptide (pHSJ1: EAYEVLSDKHKREIYD), representing the most conserved part of all J domains thus far identified—among them the Drosophila tumor suppressor Tid56—were used in immunohistochemical analyses of frozen sections of synovial tissue and immunoblotting of protein extracts of adherent synovial cells. IgG specific for Tid56 was also used. Results Both antisera predominantly and intensely stained synovial lining cells from RA patients; other cells did not stain or stained only faintly.…

AdultMalePathologymedicine.medical_specialtyMolecular Sequence DataImmunologyEnzyme-Linked Immunosorbent Assaymedicine.disease_causeAutoimmunityArthritis RheumatoidImmunoenzyme TechniquesMiceBacterial ProteinsRheumatologyAntibody SpecificityOsteoarthritismedicineAnimalsHumansImmunology and AllergyPharmacology (medical)Amino Acid SequenceCells CulturedHeat-Shock ProteinsAgedAntiserumFrozen section procedurebiologybusiness.industrySynovial MembraneHSP40 Heat-Shock ProteinsMiddle AgedIn vitromedicine.anatomical_structureSynovial Cellbiology.proteinImmunohistochemistryFemaleSynovial membraneAntibodybusinessArthritis & Rheumatism
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Immunonephelometric determination of the C4b-binding protein.

1993

A fully mechanised immunonephelometric method for the rapid and specific determination of C4b-binding protein (C4b-BP) in citrated plasma is described. The method utilizes commercially available rabbit antiserum against human C4b-BP and a nephelometer analyser. A single determination can be performed within 6 min, requiring 80 microliters sample volume. The measuring range is about 10 to 200% of normal C4b-BP. Precision is characterized by intraassay coefficients of variation between 1.5% and 2.8%, and interassay coefficients of variation between 4.0% and 4.6% for the same C4b-BP concentrations. The nephelometry of C4b-BP was correlated with electroimmunodiffusion (Laurell technique; r = 0.…

AdultMalePercentileImmunodiffusionAnalytical chemistryAdministration Oralchemical and pharmacologic phenomenaFibrinogenRabbit antiserumNephelometry and TurbidimetryBlood plasmamedicineComplement C4bHumansAgedGlycoproteinsInflammationComplement Inactivator ProteinsChromatographyChemistryC4b-binding proteinHeparinHealthy subjectsAnticoagulantsHematologyMiddle AgedEvaluation Studies as TopicFemaleCarrier ProteinsQuantitative analysis (chemistry)Nephelometrymedicine.drugThrombosis research
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Characterization of epitopes recognized by Candida factor 1 and 9 antisera by use of Saccharomyces cerevisiae mnn mutants

1993

The use of Saccharomyces cerevisiae mnn mutants has facilitated the study of the epitopes recognized by antisera against several antigenic factors of the genus Candida (Candida Check; Iatron Laboratories, Tokyo, Japan). We have taken advantage of the very well characterized structure of the mannans of the different mnn mutants to compare their reactivities with the factor antisera used in the identification of different species of the genus Candida. The results of this study provide evidence that one of the antigenic determinants recognized by factor 1 antisera is the O-linked mannose chains of the cell wall mannoproteins, while that recognized by factor 9 antiserum is the alpha 1-6-linked …

AgglutinationAntigenicityAntigens FungalMolecular Sequence DataImmunologyMutantSaccharomyces cerevisiaeMannoseEnzyme-Linked Immunosorbent AssaySaccharomyces cerevisiaeBiologyMicrobiologyEpitopeMicrobiologyMannansEpitopeschemistry.chemical_compoundAntigenAnimalsAntibodies FungalCandidaMannanAntiserumImmune Serabiology.organism_classificationInfectious DiseasesCarbohydrate SequenceBiochemistrychemistryMutationParasitologyRabbitsResearch ArticleInfection and Immunity
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Exploring alternative hapten tethering sites for high-affinity anti-picoxystrobin antibody generation

2011

The relevance of the linker tethering site in haptens was investigated for antibody generation and immunoassay development. Three derivatives of the strobilurin fungicide picoxystrobin were synthesized with the same functionalized spacer arm located at three different positions. Protein conjugates of those haptens were employed as immunogens, and novel polyclonal antibodies were produced and characterized. All haptens afforded highly specific antibodies, but different affinities to the free analyte were observed among the obtained antisera. Next, competitive enzyme-linked immunosorbent assays were studied in several formats, and site heterology was confirmed as an effective strategy for det…

AnalytePyridinesFungicideAntibody AffinityBiophysicsEnzyme-Linked Immunosorbent AssayBiochemistryAntibodiesmedicineStrobilurinmedia_common.cataloged_instanceEuropean unionMolecular Biologymedia_commonPolyclonal antibodyAntiserumDetection limitImmunoassayBinding SitesChromatographyMolecular Structuremedicine.diagnostic_testbiologyChemistryHapten synthesisCell BiologyStrobilurinsPesticideAcrylatesSoybean analysisPolyclonal antibodiesImmunoassaybiology.proteinELISAHaptensHaptenLinker
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The glycolytic enzyme glyceraldehyde-3-phosphate dehydrogenase of Candida albicans is a surface antigen.

1997

A lambda gt11 cDNA library from Candida albicans ATCC 26555 was screened by using pooled sera from two patients with systemic candidiasis and five neutropenic patients with high levels of anti-C. albicans immunoglobulin M antibodies. Seven clones were isolated from 60,000 recombinant phages. The most reactive one contained a 0.9-kb cDNA encoding a polypeptide immunoreactive only with sera from patients with systemic candidiasis. The whole gene was isolated from a genomic library by using the cDNA as a probe. The nucleotide sequence of the coding region showed homology (78 to 79%) to the Saccharomyces cerevisiae TDH1 to TDH3 genes coding for glyceraldehyde-3-phosphate dehydrogenase (GAPDH), …

Antigens FungalDNA ComplementaryGenes FungalMolecular Sequence DataBiologyMicrobiologystomatognathic systemCell WallComplementary DNACandida albicansmedicineHumansCloning MolecularCandida albicansFluorescent Antibody Technique IndirectMolecular BiologyGlyceraldehyde 3-phosphate dehydrogenaseAntibodies FungalAntiserumcDNA libraryCandidiasisAntibodies MonoclonalGlyceraldehyde-3-Phosphate Dehydrogenasesmedicine.diseasebiology.organism_classificationMolecular biologyCorpus albicansBlotting SouthernBiochemistryPolyclonal antibodiesAntigens Surfacebiology.proteinSystemic candidiasisGlycolysisResearch Article
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Polyclonal antibodies to mannan from yeast also recognize the carbohydrate structure of gp120 of the AIDS virus: an approach to raise neutralizing an…

1990

This study initiates a new method of developing an antigen which might be useful in the prevention of HIV-1 infection. Using a mannan preparation from Saccharomyces cerevisiae neutralizing antiserum was raised in rabbits which prevents HIV-1 infection in vitro up to a titre of 1:128. The corresponding antibody preparation neutralized the in vitro infectivity down to a concentration of 5 micrograms/ml. Analytical studies suggest that the antibodies are directed against the mannose residues of the HIV-1 glycoprotein (gp) 120 and its precursor gp 160.

Antigens FungalImmunologyCarbohydratesSaccharomyces cerevisiaeHIV AntibodiesHIV Envelope Protein gp120In Vitro TechniquesVirusCell LineMannansAntigenNeutralization TestsImmunology and AllergyAnimalsMannanAntiserumInfectivityAcquired Immunodeficiency SyndromeBinding SitesbiologyChemistryPrimary and secondary antibodiesVirologyInfectious DiseasesPolyclonal antibodiesbiology.proteinHIV-1FemaleRabbitsAntibodyAIDS (London, England)
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A Trisialoganglioside Containing a Sialyl α2-6 N-Acetylgalactosamine Residue Is a Cholinergic-Specific Antigen, Chol-1α1

1992

Cholinergic-specific antigens termed the Chol-1 family have been suggested to be of a ganglioside nature by Richardson et al. (J. Neurochem. 38, 1605-1614, 1982). Two molecular species of polysialogangliosides among bovine brain gangliosides were found to react with anti-Chol-1 alpha antiserum. One of them, Chol-1 alpha-a, was isolated and characterized as a trisialoganglioside containing the gangliotetraose backbone in which 1 mol of sialic acid was attached to each of the reducing end galactose, N-acetylgalactosamine and internal galactose residues, respectively. The chemical structure of Chol-1 alpha-a was determined for the first time, being as follows: IV3NeuAc III6NeuAc II3NeuAc-GgOse…

AntiserumGangliosidetechnology industry and agricultureGeneral MedicineBiologyBiochemistryN-AcetylgalactosamineSialic acidchemistry.chemical_compoundResidue (chemistry)chemistryAntigenBiochemistryGalactosepolycyclic compoundsCholinergiclipids (amino acids peptides and proteins)Molecular BiologyThe Journal of Biochemistry
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Preliminary characterization of the material released to the culture medium by Candida albicans yeast and mycelial cells.

1995

Culture filtrate concentrates were obtained from Candida albicans yeast and mycelial cells grown in the presence of 14C-protein hydrolysate for radioactive labeling of cellular polypeptides. Both growth forms released to the medium minor but significant amounts of proteinaceous materials. The analysis of culture filtrate concentrates by means of SDS-polyacrylamide gel electrophoresis and fluorography revealed a similar and complex electrophoretic pattern, though some qualitative and quantitative differences between samples obtained from yeast and mycelial cells were observed. Materials released, mostly composed of mannoproteins as shown by their affinity towards concanavalin A, presented (i…

AntiserumGel electrophoresisMembrane GlycoproteinsbiologyBlotting WesternGeneral MedicineCross Reactionsbiology.organism_classificationMicrobiologyYeastHydrolysateCell wallFungal ProteinsBiochemistryPolyclonal antibodiesConcanavalin ACell WallCulture Media ConditionedCandida albicansbiology.proteinElectrophoresis Polyacrylamide GelCandida albicansMolecular BiologyAntibodies FungalFiltrationAntonie van Leeuwenhoek
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Effect of antibodies against cytochrome P-450 on demethylation and denitrosation of N-nitrosodimethylamine and N-nitrosomethylaniline.

1988

Rat liver microsomes which were induced either with ethanol or PB were incubated with NDMA or NMA. Formaldehyde generation and nitrite formation were measured as metabolic parameters for oxidative bioactivation and denitrosation, respectively. The influence of antiserum PB3a1 and PB22 containing antibodies against the corresponding cytochrome P-450 species on both metabolic functions was investigated. The results showed that the influence on formaldehyde production and denitrosation varied independently in that both parameters were either not affected, or influenced in an opposite way, or inhibited to a different degree. Especially remarkable was the 80% inhibition of formaldehyde generatio…

AntiserumMaleCancer ResearchEthanolNitrosaminesCytochromebiologyChemistryRats Inbred StrainsGeneral MedicineMetabolismAntibodiesDimethylnitrosamineRatsIsoenzymeschemistry.chemical_compoundOncologyBiochemistryCytochrome P-450 Enzyme SystemN-NitrosodimethylamineMicrosomebiology.proteinAnimalsNitriteDemethylationJournal of cancer research and clinical oncology
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