Search results for "Poly(acrylamide)"

showing 10 items of 377 documents

Equilibrium swelling and solvation studies on crosslinked polyacrylamides

2004

Polyacrylamide (PA) crosslinked with four different crosslinking agents, triethyleneglycol dimethacrylate (TEGDMA), N,N′-methylene bisacrylamide (NNMBA), hexanediol dimethacrylate (HDDMA) and divinylbenzene (DVB), with mole percents ranging from 5 to 20, was prepared by solution polymerization and subjected to swelling and solvation studies. Solubility parameters and cohesive energy density were determined from swelling studies. Molecular weight between crosslinks for these systems were determined by Flory–Rehner analysis. There is a discontinuous volume change for 10% NNMBA and HDDMA crosslinked PA, 15% TEGDMA crosslinked PA and 10 and 15% DVB crosslinked PA in solvent mixtures of acetic a…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsOrganic ChemistryPolyacrylamideSolvationSolution polymerizationPolymerDivinylbenzenechemistry.chemical_compoundHildebrand solubility parameterchemistrySelf-healing hydrogelsPolymer chemistryMaterials ChemistrymedicineSwellingmedicine.symptomPolymer International
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Chain Stiffness of Elastin-Like Polypeptides

2010

The hydrodynamic radii of a series of genetically engineered monodisperse elastin like polypeptides (ELP) was determined by dynamic light scattering in aqueous solution as function of molar mass. Utilizing the known theoretical expression for the hydrodynamic radius of wormlike chains, the Kuhn statistical segment length was determined to be lk = 2.1 nm, assuming that the length of the peptide repeat unit was b = 0.365 nm, a value derived for a coiled conformation of ELP. The resulting chain stiffness is significantly larger than previously reported by force-distance curve analysis (lk < 0.4 nm). The possible occurrence of superstructures, such as hairpins or helices, would reduce the conto…

chemistry.chemical_classificationMolar massHydrodynamic radiusPolymers and PlasticsbiologyDispersityBioengineeringPeptideArticleElastinMolecular WeightBiomaterialsDynamic light scatteringChain (algebraic topology)chemistryPolymer chemistryHydrodynamicsMaterials ChemistryBiophysicsbiology.proteinElectrophoresis Polyacrylamide GelPeptidesElastinRepeat unitBiomacromolecules
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Use of two-dimensional thin-layer chromatography for the components study of poly(adenosine diphosphate ribose)

1990

Two-dimensional thin-layer chromatography on cellulose plates has been used for separating and quantifying the three adenosine derivatives: AMP, phosphoribosyl AMP (PRAMP), and (PR)2AMP obtained by venom phosphodiesterase digestion of poly(ADP-ribose). In vitro synthesized polymer, up to 300 derivatives in length were studied. Some parameters of the complexity of poly(ADP-ribose) could be deduced from our results: (i) The first branching point appears in fragments of approximately 21 derivatives in length. (ii) The branching points are located at regular distances of approximately 41 derivatives from each other.

chemistry.chemical_classificationPoly Adenosine Diphosphate RiboseChromatographyPolymersChemistryBiophysicsPoly Adenosine Diphosphate RiboseCell BiologyBranching pointsPolymerBiochemistryAdenosineAdenosine MonophosphateIn vitroThin-layer chromatographyVenom phosphodiesterasechemistry.chemical_compoundmedicineElectrophoresis Polyacrylamide GelChromatography Thin LayerCelluloseMolecular Biologymedicine.drugAnalytical Biochemistry
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Controlled cleavage of KLH1 and KLH2 by the V8 protease from Staphylococcus aureus reassociation, electrophoretic and transmission electron microscop…

1999

The reassociation behaviour of protease V8-cleaved peptides from KLH1 and KLH2, the two hemocyanin isoforms from the giant keyhole limpet Megathura crenulata, has been studied by transmission electron microscopy of negatively stained specimens and SDS/PAGE. Reassociation of the complete mixture of protease cleavage products and of combinations of peptide fragments purified by HPLC was performed in the presence of 100 mm CaCl2 and 100 mm MgCl2 at pH 7.4, over a period of 1 to 4 weeks. The V8 protease splits KLH1 into peptide fragments containing the functional units abc, def, defg, defgh, g and h. This mixture of peptide fragments reassociated to form helical tubular polymers, with a diamete…

chemistry.chemical_classificationProteasebiologyStereochemistrymedicine.medical_treatmentProtein subunitHydrolysisSerine EndopeptidasesHemocyaninPeptideMegathura crenulatabiology.organism_classificationCleavage (embryo)BiochemistryPeptide FragmentsMicroscopy ElectronBiochemistrychemistryPolymerizationHemocyaninsmedicineProtein IsoformsElectrophoresis Polyacrylamide GelPolyacrylamide gel electrophoresisEuropean journal of biochemistry
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Two proteases from nuclei of rat testis cells. I. Isolation

1987

Abstract Two proteases, assayed with fluorogenic peptides and tentatively designated Rc and Kc, have been isolated from nuclei of rat testis cells by differential extraction with acetic acid, removal of some proteins at pH 4.5, and polyacrylamide gel electrophoresis followed by electroblotting onto nitrocellulose paper. Protease R hydrolyzes t‐Butyl‐oxycarbonyl‐Val‐Pro‐Arg‐7‐amino‐4‐methyl‐coumarin and other peptides in which arginine is joined to 7‐amino‐4‐methyl‐coumarin by amide linkage. Protease Kc has a preference for peptides terminating in lysine‐7‐amino‐4‐methylcoumarin amide. Neither of these proteases is active against Glu‐Phe‐7‐amino‐4‐methyl‐coumarin amide or Carbobenzoxy‐Arg‐7‐…

chemistry.chemical_classificationProteasesProteaseArgininemedicine.medical_treatmentBiologyMolecular biologychemistry.chemical_compoundHydrolysisEnzymechemistryBiochemistrymedicineAnimal Science and ZoologyTrichloroacetic acidPolyacrylamide gel electrophoresisElectroblottingBollettino di zoologia
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Biochemical identification and tissue-specific expression patterns of keratins in the zebrafish Danio rerio

1998

We have identified a number of type I and type II keratins in the zebrafish Danio rerio by two-dimensional polyacrylamide gel electrophoresis, complementary keratin blot-binding assay and immunoblotting. These keratins range from 56 kDa to 46 kDa in molecular mass and from pH 6.6 to pH 5.2 in isoelectric point. Type II zebrafish keratins exhibit significantly higher molecular masses (56-52 kDa) compared with the type I keratins (50-48 kDa), but the isoelectric points show no significant difference between the two keratin subclasses (type II: pH 6.0-5.5; type I: pH 6.1-5.2). According to their occurrence in various zebrafish tissues, the identified keratins can be classified into "E" (epider…

chemistry.chemical_classificationanimal structuresHistologyintegumentary systembiologyMolecular massCellular differentiationDanioCell Biologybiology.organism_classificationMolecular biologyPathology and Forensic MedicineIsoelectric pointMicroscopy FluorescenceBiochemistrychemistryGenetic modelKeratinAnimalsKeratinsTissue DistributionPolyacrylamide gel electrophoresisZebrafishCytoskeletonZebrafishCell and Tissue Research
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Expression of silicatein in spicules from the Baikalian sponge

2005

Lake Baikal harbors the largest diversity of sponge species [phylum Porifera] among all freshwater biotopes. The abundantly occurring species Lubomirskia baicalensis was used to study the seasonal silicatein metabolism; the spicules of this species have an unusually thick axial filament, consisting of silicatein, which remains constant in diameter during their growth. In the course of maturation, the size of the silicic acid shell grows, until the final diameter of the spicules of about 8 microm is reached. The seasonal content of silicatein was assessed by use of antibodies raised against silicatein; they stained specifically the axial filaments. In addition we determined, by application o…

chemistry.chemical_classificationbiologyEcologyRNACell BiologyGeneral Medicinebiology.organism_classificationMolecular biologyAmino acidSpongeEnzymeSponge spiculechemistryPeptide sequenceGenePolyacrylamide gel electrophoresisCell Biology International
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Biochemical Characterization of an Acetylcholine-hydrolyzing Enzyme from Bean Seedlings.

1980

An acetylcholine hydrolyzing enzyme was prepared and purified (40 times) from dwarf bean hypocotyl hooks. The purity of the enzyme was proved by polyacrylamide gel electrophoresis. The molecular weight of the enzyme was determined to be 65,000 daltons. Enzyme activity was the highest at pH 8.0 and between 30 and 36 C. The enzyme had an apparent affinity constant (K(m)) for acetylcholine of 460/micromolar. The affinity for substrate analogs increased from butyrylthiocholine to propionylthiocholine to acetylthiocholine. The enzyme activity was inhibited by choline, neostigmine, physostigmine, manganese, and calcium. Magnesium had no influence on the enzyme activity. We conclude that the enzym…

chemistry.chemical_classificationbiologyPhysiologySubstrate (chemistry)food and beveragesPlant ScienceArticlesAcetylcholinesteraseEnzyme assayButyrylthiocholinechemistry.chemical_compoundEnzymechemistryBiochemistryAcetylthiocholineGeneticsbiology.proteinmedicinePolyacrylamide gel electrophoresisAcetylcholinemedicine.drugPlant physiology
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Untersuchungen über die radikalpolymerisation von acrylamid

1954

Verschiedene Methoden zur Radikal-Polymerisation von Acrylamid mit und ohne Losungsmittel werden beschrieben. Die durch γ-Strahlen ausgeloste Polymerisation ergibt sehr hochmolekulare Polymerisate; dagegen haben die mittels Fenton-Reagens erhaltenen Produkte nur sehr geringe spezifische Viskositat. Ultraschall wirkt auf das Monomere polymerisierend und auf das Polymere depolymerisierend. Aus den Viskositatskurven eines reinen Polymerisates und seiner Fraktionen ist zu schliesen, das solche Polyacrylamide in wasriger Losung als homoopolare Molekulkolloide vorliegen. Different methods of radical-polymerization of acrylamide in solution and in bulk are described. The γ-rays induced polymerizat…

chemistry.chemical_classificationchemistry.chemical_compoundMonomerAqueous solutionchemistryPolymerizationReagentIntrinsic viscosityAcrylamidePolyacrylamidePolymer chemistryPolymerDie Makromolekulare Chemie
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Über die polymerisation von acrylsäurechlorid

1960

Monomeres Acrylsaurechlorid wird mittels Azodiisobuttersaurenitril in Dioxan bei 50°C polymerisiert. Bei Ausschlus von Feuchtigkeit und Sauerstoff entstehen bis zu 90% Umsatz unvernetzte Polymere. Durch Reaktion mit flussigem Ammoniak wurden Polyacrylamide erhalten, die zur viskosimetrischen Molgewichtsbestimmung dienten. Monomeric acrylyl chloride was polymerized in dioxane at 50°C by azo-bis-isobutyronitrile. With the exclusion of moisture and oxygen, a non-cross-linked polymer with a 90% yield was obtained. Polyacrylamides were formed by the reaction of polyacrylyl chloride with liquid ammonia. These products were used for viscosimetric molecular weight determinations.

chemistry.chemical_classificationchemistry.chemical_compoundMonomerchemistryPolymerizationYield (chemistry)PolyacrylamideLiquid ammoniaPolymer chemistrymedicinePolymerChloridemedicine.drugDie Makromolekulare Chemie
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