Search results for "acrylamide"

showing 10 items of 485 documents

Notizen: Unterschiedliche Desoxyribonuclease-Aktivitäten im Seminalplasma von Bullen/Different Deoxyribonuclease-Activities in Bull Seminal Plasma

1976

By means of the in situ assay of deoxyribonucleases in DNA-containing polyacrylamide gels after separation by micro-disc-electrophoresis different deoxyribonucleases are detectable in bull seminal plasma. There are two groups of acid deoxyribonuclease-activities with a pH optimum at pH 5.0, one with a pH optimum at pH 7.4 and an additional one with a pH optimum at pH 8.5.

chemistry.chemical_compoundChromatographychemistryPh optimumPolyacrylamideDeoxyribonucleaseDeoxyribonucleasesGeneral Biochemistry Genetics and Molecular BiologyZeitschrift für Naturforschung C
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Monomere und polymere Succinimidoester von ω-Methacryloylaminosäuren, ihre Darstellung und ihre Reaktion mit Aminen

1978

Mit der in dieser Arbeit beschriebenen Synthese von ω-Methacryloylaminosaure-succinimidoestern (1) wurden Monomere erhalten, die leicht mit Methacrylamid copolymerisiert werden konnten. Die entstandenen Copolymeren, die als Trager fur Enzyme und Pharmaka verwendet werden konnen, tragen die selektiv mit Aminen reagierende Succinimidoester-Gruppe an einem “Spacerarm”. Die Reaktionsfahigkeit der neuen Monomeren gegenuber verschiedenen Aminen wurde untersucht. The synthesis of succinimido esters of ω-methacryloylaminocarboxylic acids affords monomers which can easily be copolymerized with methacrylamide. The resulting copolymers have a succinimido ester group fixed on a “spacer arm”, which reac…

chemistry.chemical_compoundColloid and Surface ChemistryMonomerPolymers and PlasticsChemistryPolymer chemistryMaterials ChemistryCopolymerMethacrylamideReactivity (chemistry)Physical and Theoretical ChemistryColloid and Polymer Science
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Polyacrylamide Electrophoresis: A Preparative Technique and its Application in Complement Chemistry

1971

chemistry.chemical_compoundElectrophoresisChromatographychemistryPolyacrylamideGel electrophoresis of proteinsComplement (complexity)
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Ultrarotspektroskopische Untersuchungen an Copolymeren des Acroleins. Polymere Acroleine. 12. Mitteilung

1959

Die UR-Spektren folgender Copolymerisate werden mitgeteilt: Acrolein/Acrylnitril, Acrolein/Acrylsauremethylester, Acrolein/Vinylaceatat und Acrolein/Acrylamid. Am Beispiel der Copolymeren von Acrolein und Acrylnitril wird gezeigt, das man durch Intensitatsmessungen der UR-Absorptionsbanden zu quantitativen Aussagen uber Anordnung und Lange der einzelnen Segmente im Copolymeren gelangen kann. Die so erhaltenen Ergebnisse stimmen mit statistischen Berechnungen uberein. The infrared spectra of the following copolymers are given: acrolein/acrylonitrile, acrolein/methylacrylate, acrolein/vinylaetate and acrolein/acrylamide. There is shown by the example of copolymers of acrolein and acrylonitile…

chemistry.chemical_compoundchemistryAcrylamideAcroleinPolymer chemistryCopolymerInfrared spectroscopyAcrylonitrileDie Makromolekulare Chemie
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Über die copolymerisation des acroleins und des methacroleins in homogener lösung. Polymere acroleine. 25. Mitt.

1962

Die Copolymerisation des Acroleins und des Methacroleins in Dimethylformamid sowie in Dioxan wird beschrieben. Die Parameter folgender Systeme wurden bestimmt: Acrolein/Acrylnitril (r1 = 1,60; r2 = 0,52); Acrolein/Acrylamid (r1 = 1,69; r2 = 0,21); Acrolein/Methacrylnitril (r1 = 0,72; r2 = 1,20); Acrolein/2-Vinylpyridin (r1 = 4; r2 = 0) und Methacrolein/Methacrylnitril (r1 = 1,78; r2 = 0,40). Die Berechnung der Q-und e-Werte bzw. der q- und ϵ-Werte ergab fur Acrolein: Q = 0,64; e = 0,61; q = -2,8 kcal/Mol; ϵ = 0,19 = 10−10 elektrostatische Einheiten und fur Methacrolein: Q = 1,59; e = 0,36; q = −3,4 kcal/Mol; ϵ = 0,11 = 10−10 elektrostatische Einheiten. The copolymerisation of acrolein and m…

chemistry.chemical_compoundchemistryAcrylamidePolymer chemistryAcroleinDimethylformamideReactivity (chemistry)MethacroleinDie Makromolekulare Chemie
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S-type lectins occur also in invertebrates: high conservation of the carbohydrate recognition domain in the lectin genes from the marine sponge Geodi…

1993

The marine sponge Geodia cydonium contains several lectins. The main component, called lectin-1, is composed of three to four identical subunits. The subunits of the lectins were cloned from a cDNA library; two clones were obtained. From the deduced aa sequence of one clone, LECT-1, a mol. wt of 15,313 Da is calculated; this value is in good agreement with mass spectrometric analysis of 15,453 +/- 25 Da. The sequence of another clone, LECT-2, was analysed and the aa sequence was deduced (15,433 Da). The two subunits have a framework sequence of 38 conserved aa which are characteristic for the carbohydrate-binding site of vertebrate S-type lectins. Clustering of lectin sequences of various s…

clone (Java method)GalectinsBlotting WesternMolecular Sequence DataBiochemistryChromatography AffinityMass SpectrometryLectinsAnimalsAmino Acid SequenceCloning MolecularPeptide sequenceGeneGalectinCloningbiologyBase SequencecDNA libraryLectinDNAbiology.organism_classificationPoriferaSuberites domunculaBiochemistrybiology.proteinElectrophoresis Polyacrylamide GelGlycobiology
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Spine and test skeletal matrices of the Mediterranean sea urchinArbacia lixula- a comparative characterization of their sugar signature

2015

15 pages; International audience; Calcified structures of sea urchins are biocomposite materials that comprise a minor fraction of organic macromolecules, such as proteins, glycoproteins and polysaccharides. These macromolecules are thought to collectively regulate mineral deposition during the process of calcification. When occluded, they modify the properties of the mineral. In the present study, the organic matrices (both soluble and insoluble in acetic acid) of spines and tests from the Mediterranean black sea urchin Arbacia lixula were extracted and characterized, in order to determine whether they exhibit similar biochemical signatures. Bulk characterizations were performed by mono-di…

echinoidPolysaccharideBiochemistryMineralization (biology)Calcium Carbonate[SDV.BBM.GTP]Life Sciences [q-bio]/Biochemistry Molecular Biology/Genomics [q-bio.GN]Spectroscopy Fourier Transform InfraredMediterranean SeaAnimalsMonosaccharide[SDV.IB.BIO]Life Sciences [q-bio]/Bioengineering/BiomaterialsMolecular BiologyArbacia lixulaPolyacrylamide gel electrophoresisorganic matrixArbaciachemistry.chemical_classificationsaccharideArbaciabiologyLectinlectin assayCell Biology[ SDV.IB.BIO ] Life Sciences [q-bio]/Bioengineering/Biomaterialsbiomineralizationbiology.organism_classificationchemistryBiochemistry[ SDV.BBM.GTP ] Life Sciences [q-bio]/Biochemistry Molecular Biology/Genomics [q-bio.GN]AgglutininsSea UrchinsMicroscopy Electron Scanningbiology.proteinElectrophoresis Polyacrylamide GelBiomineralizationFEBS Journal
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F-type lectin from the sea bass (Dicentrarchus labrax): purification, cDNA cloning, tissue expression and localization, and opsonic activity.

2009

Recently described biochemical and structural aspects of fucose-binding lectins from the European eel (Anguilla anguilla) and striped bass (Morone saxatilis) led to the identification of a novel lectin family ("F-type" lectins) characterized by a unique sequence motif and a characteristic structural fold. The F-type fold is shared not only with other members of this lectin family, but also with apparently unrelated proteins ranging from prokaryotes to vertebrates. Here we describe the purification, biochemical and molecular properties, and the opsonic activity of an F-type lectin (DlFBL) isolated from sea bass (Dicentrarchus labrax) serum. DlFBL exhibits two tandemly arranged carbohydrate-r…

food.ingredientDNA ComplementaryImmunoblottingAquatic ScienceChromatography AffinityBass (fish)F-type lectin; Dicentrarchus labrax;teleost;emaggluthinins opsoninfoodPhagocytosisOpsonin ProteinsComplementary DNALectinsEnvironmental ChemistryAnimalsDicentrarchus labraxRNA MessengerSea bassCloning MolecularOpsoninemaggluthinins opsoninPhylogenyteleostbiologyBase SequenceLectinGeneral MedicineOpsonin Proteinsbiology.organism_classificationMolecular biologyGene Expression RegulationImmunologybiology.proteinMacrophages PeritonealF lectin sea bass inflammationDicentrarchusBassElectrophoresis Polyacrylamide GelSequence motifF-type lectinFishshellfish immunology
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Induction of Hsp70 by the Herbicide Oxyfluorfen (Goal) in the Egyptian Nile Fish, Oreochromis niloticus

1999

This paper deals with the expression of the biomarker hsp70 in the liver and kidney of the freshwater fish Oreochromis niloticus following exposure to the herbicide oxyfluorfen (Goal). Fishes were exposed to three concentrations, the 96-h LC50 (3 mg/L), the 96-h (1/2)LC50 (1.5 mg/L), and the 96-h (1/4)LC50 (0.75 mg/L) of oxyfluorfen for 6, 15, and 24 days, respectively, and samples were taken at three different time periods for each concentration. The livers responded to the herbicide by an induction of the expression of both the constitutive (hsp75; Mr 75 kDa) and the inducible (hsp73; Mr 73 kDa) hsp70 proteins. In kidney, the herbicide induced a time-dependent increase in the expression o…

food.ingredientHealth Toxicology and MutagenesisBiologyKidneyToxicologyAnimal sciencefoodHalogenated Diphenyl EthersAnimalsEcotoxicologyHSP70 Heat-Shock ProteinsIncubationEcologyPhenyl EthersTilapiaGeneral MedicinePesticidebiology.organism_classificationPollutionHsp70OreochromisLiverToxicityFreshwater fishEgyptElectrophoresis Polyacrylamide GelTilapiaArchives of Environmental Contamination and Toxicology
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Wall mannoproteins in cells from colonial phenotypic variants of Candida albicans.

1990

Candida albicans ATCC 26555 switched at high frequency (10(-1) to 10(-3)) between several phenotypes identified by colony morphology on a defined mineral amino-acid-containing agar medium supplemented with arginine and zinc (LAZ medium). When cells taken from colonies exhibiting distinct morphologies were plated directly onto LAZ agar, spontaneous conversion to all the variant phenotypes occurred at combined frequencies of 2.1 x 10(-1) to 9.5 x 10(-3). However, when cells taken from the different colonial phenotypes were plated directly onto an undefined medium (yeast extract/peptone/dextrose; YPD medium), or first incubated in liquid YPD medium and then cloned on YPD agar, all colonies obs…

food.ingredientHydrolasesPhenotypic switchingMicrobiologyMicrobiologyAgar plateCell wallFungal Proteinschemistry.chemical_compoundfoodCell WallCandida albicansConcanavalin AAgarCandida albicansAntiserumGrowth mediumMembrane GlycoproteinsbiologyTemperaturebiology.organism_classificationYeastCulture MediaPhenotypechemistryElectrophoresis Polyacrylamide GelJournal of general microbiology
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