Search results for "acrylamide"

showing 10 items of 485 documents

ADAMTS13 In 4 Different VWF/VIII Concentrates and Its Impact on Therapy.

2010

Abstract Abstract 3677 Introduction: The hemostatic activity of von Willebrand Factor (VWF) is mainly controlled by the plasma metalloprotease ADAMTS13, which cleaves ultralarge VWF multimers. A qualitative or quantitative deficiency of VWF induces the most common hemorrhagic diathesis, the von Willebrand Disease (VWD). The current classification graduates the VWD in three major types. Depending on severity and the type of VWD the treatment with VWF/FVIII concentrates may by necessary. The commercially available VWF/FVIII concentrates differ in their multimer structure and furthermore also in their pharmacokinetics. We investigated commercial VWF concentrates with respect to their ADAMTS 13…

Gel electrophoresisbiologyChemistryImmunologyCell BiologyHematologymedicine.diseaseBiochemistryMolecular biologyADAMTS13SepharoseAntigenVon Willebrand factorhemic and lymphatic diseasesVon Willebrand diseasemedicinebiology.proteinAntibodyPolyacrylamide gel electrophoresisBlood
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Molecular size and net charge of pathogenesis-related enzymes from barley (Hordeum vulgare L., v. Karat) infected withDrechslera teres f. teres (Sacc…

1998

Molecular size and net charge of isoforms of pathogenesis-related (PR) chitinase, beta-1,3-glucanase and peroxidase were studied in uninfected barley (Hordeum vulgare L., v. Karat) leaves and in barley leaves infected with the pathogenic fungus Drechslera teres f. teres (Sacch.) Shoem. Molecular characteristics were determined by time-dependent polyacrylamide gradient gel electrophoresis under native conditions and by applying an extended version of the computer program MOL-MASS (Rothe, G. M., Weidmann, H., Electrophoresis 1991, 12, 703-709). Uninfected barley leaves contained predominantly one peroxidase isozyme but also three very weak peroxidases. Activities of all of these three peroxid…

Gel electrophoresisbiologyMolecular massbeta-GlucosidaseChitinasesClinical BiochemistryHordeumGlucan 13-beta-GlucosidaseGlucanasebiology.organism_classificationBiochemistryIsozymeHelminthosporiumAnalytical ChemistryMolecular WeightBiochemistryChitinasebiology.proteinElectrophoresis Polyacrylamide GelDrechsleraHordeum vulgarePeroxidasePeroxidaseElectrophoresis
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Effect of α-factor on individual wall mannoproteins fromSaccharomyces cerevisiae acells

1985

Treatment of Saccharomyces cerevisiae a cells with α-factor partially inhibits mannosylation of the high Mr mannoproteins, although there is an increase in the total amount of these molecules present in the wall. They show a similar mobility in SDS-acrylamide gels to those from untreated mnn2 cells. No other significant effects on wall mannoproteins have been observed, except a decrease in the amount of the 29 kDa species.

Gel electrophoresisbiologySaccharomyces cerevisiaebiology.organism_classificationMicrobiologyYeastcarbohydrates (lipids)Cell wallAgglutination (biology)Endoglycosidase Hchemistry.chemical_compoundBiochemistrychemistryMannosylationAcrylamideGeneticsbiology.proteinMolecular BiologyFEMS Microbiology Letters
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Determination of molecular weights and Stokes' radii of non-denatured proteins by polyacrylamide gradient gel electrophoresis. 2. Determination of th…

1982

Under certain conditions in polyacrylamide gradient gel electrophoresis (PAGGE), a linear correlation between the logarithm of the size of calibration proteins (log MW or log Rs) and the square root of their migration distance (√D) can be observed; slope and intercept of the calibration curve depend on the duration of electrophoresis; linearity, however, is maintained over a wide range (4-60 h, 200 V) (Rothe and Purkhanbaba, Electrophoresis 1982, 3, 33–42.) Using this method the reaction of plant isozyme systems penetrating a linear polyacrylamide (PAA) gradient gel was investigated: lactate dehydrogenase (LDH) from potato tubers behaves similarly to animal calibration proteins. The enzyme …

Gel electrophoresischemistry.chemical_classificationChromatographyMolecular massChemistryCalibration curveClinical BiochemistryPolyacrylamideAnalytical chemistryBiochemistryIsozymeAnalytical Chemistrychemistry.chemical_compoundElectrophoresisMolecular-weight size markerOxidoreductaseElectrophoresis
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Determination of molecular weights and Stokes' radii of non-denatured proteins by polyacrylamide gradient gel electrophoresis 3. Estimation of the up…

1985

Studying the separation behavior of various native carbonic anhydrase isozymes from mammalian erythrocytes we found that the migration of these enzymes differs from that of the marker proteins commonly used in gradient gel electrophoresis. In alkaline buffer systems the enzymes from human, bovine, rabbit, and canine erythrocytes start to migrate with a size apparently 6 to 12 times larger than their monomeric size, then gradually lose in apparent size and finally end up in a size equivalent to their monomeric mol mass. We determined the monomeric mol mass of the various carbonic anhydrase forms to be 23 000 to 39 000 (g/mol). These values are in accordance with different data in the literat…

Gel electrophoresischemistry.chemical_classificationChromatographyMolecular massbiologyChemistryClinical BiochemistryPolyacrylamideBiochemistryIsozymeAnalytical Chemistrychemistry.chemical_compoundEnzymeMolecular-weight size markerCarbonic anhydraseMolebiology.proteinElectrophoresis
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C8 Reference Typing Report and Nomenclature Recommendation

1990

Using two different typing techniques (i.e. polyacrylamide gel isoelectric focusing (PAGIF) with Western blot and SDS-polyacrylamide gel electrophoresis of precipitated C8 under nonreducing conditions with Western blot), the following observations were made during the reference typing for C81 (C8A). The Japanese variant A1J is probably identical with A1Cauc, whereas B1J is definitely different from B1Cauc and could therefore provisionally be named HB3'. Variant 'A2' from Japan is focused in an intermediate position, but different from M1 and could be named 'M2'. Both variants possess normal A subunits. B2 from Japan is clearly different from B1Cauc and should retain its designation. In PAGI…

Gel electrophoresismedicine.diagnostic_testMacromolecular SubstancesIsoelectric focusingBlotting WesternImmunologyGenetic VariationHematologyBiologyComplement C8Molecular biologyWestern blotReference ValuesTerminology as TopicmedicineHumansElectrophoresis Polyacrylamide GelTypingIsoelectric FocusingPolyacrylamide gel electrophoresisNomenclatureComplement and Inflammation
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A comparative assay of epidemiological markers for Acinetobacter strains isolated in a hospital.

1989

Summary A comparative assay for epidemiological evaluation of three different Acinetobacter typing procedures, i.e. biotyping, phagetyping, and the analysis of the bacterial envelope protein profiles, was carried out using sixty-four multiresistant Acinetobacter strains isolated from clinical specimens. The antibiotic susceptibility of the strains was also considered. After genospecies identification, biotyping allowed the recognition of a relatively large and long-lasting presence, at an Intenive Therapy Unit, of two A. baumannii biotypes. Phage-typing and the analysis of the susceptibility to antibiotics allowed for the differentiation of strains belonging to different genospecies and bio…

Gel electrophoresismedicine.medical_specialtyCross InfectionbiologyAcinetobactermedicine.drug_classImmunologyAntibioticsAcinetobacterbiology.organism_classificationMicrobiologyBacterial Typing TechniquesBacterial ProteinsItalyEpidemiologymedicineHumansNeisseriaceaeElectrophoresis Polyacrylamide GelTypingBacteriophage TypingBacteriaAcinetobacter InfectionsZentralblatt fur Bakteriologie : international journal of medical microbiology
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Developmental expression of two Haliotis asinina hemocyanin isoforms

2005

Hemocyanins are large copper-containing respiratory proteins that play a role in oxygen transport in many molluscs. In some species only one hemocyanin isoform is present while in others two are expressed. The physiological relevance of these isoforms is unclear and the developmental and tissue-specific expression of hemocyanin genes is largely unknown. Here we show that two hemocyanin genes in the gastropod Haliotis asinina, which encode H. asinina hemocyanin (HaH1) and HaH2 isoforms, are developmentally expressed. These genes initially are expressed in a small number of mesenchyme cells at trochophore and pre-torsional veliger stages, with HaH1 expression slightly preceding HaH2. These ce…

Gene isoformCancer ResearchDNA ComplementaryEmbryo Nonmammalianmedicine.medical_treatmentMolecular Sequence DataVeligermedicineAnimalsProtein IsoformsAmino Acid SequenceImmunoelectrophoresisMolecular BiologyGeneConserved SequenceIn Situ HybridizationPhylogenySequence Homology Amino AcidbiologyHaliotis asininaReverse Transcriptase Polymerase Chain ReactionOxygen transportGene Expression Regulation DevelopmentalHemocyaninCell BiologyAnatomybiology.organism_classificationCell biologyMolluscaLarvaTrochophoreHemocyaninsElectrophoresis Polyacrylamide GelDevelopmental biologyDevelopmental BiologyDifferentiation
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Purification and Characterization of the Soluble Interleukin-6 Receptor from Human Plasma and Identification of An Isoform Generated through Alternat…

1996

The soluble human interleukin-6 receptor (shIL6R) was purified from human plasma. In a single immunoaffinity purification step a 140000-fold enrichment with a yield of 95% was achieved. A subsequent IL-6 affinity chromatography resulted in a homogeneous receptor preparation but only in a yield of less than 5%. The biological activity of the soluble receptor was clearly demonstrated by its ability to induce the synthesis of the acute-phase protein α1-antichymotrypsin in HepG2 cells stably transfected with IL-6. Upon gel filtration, the native shIL6R showed an apparent molecular mass of 93 kDa. Analysis by SDS/PAGE revealed an apparent molecular mass of 65 kDa for the soluble receptor. Deglyc…

Gene isoformPeptideBiologyTransfectionBiochemistryChromatography AffinityAmidohydrolasesCell LineAffinity chromatographyAntigens CDTumor Cells CulturedHumansPeptide-N4-(N-acetyl-beta-glucosaminyl) Asparagine AmidaseRNA MessengerReceptorPeptide sequencechemistry.chemical_classificationMolecular massInterleukin-6Cell MembraneAlternative splicingReceptors InterleukinReceptors Interleukin-6Molecular biologyRecombinant ProteinsMolecular WeightAlternative SplicingBiochemistrychemistryInterleukin-6 receptorChromatography GelElectrophoresis Polyacrylamide GelEuropean Journal of Biochemistry
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Autoregulation of NFATc1/A Expression Facilitates Effector T Cells to Escape from Rapid Apoptosis

2002

AbstractThreshold levels of individual NFAT factors appear to be critical for apoptosis induction in effector T cells. In these cells, the short isoform A of NFATc1 is induced to high levels due to the autoregulation of the NFATc1 promoter P1 by NFATs. P1 is located within a CpG island in front of exon 1, represents a DNase I hypersensitive chromatin site, and harbors several sites for binding of inducible transcription factors, including a tandemly arranged NFAT site. A second promoter, P2, before exon 2, is not controlled by NFATs and directs synthesis of the longer NFATc1/B+C isoforms. Contrary to other NFATs, NFATc1/A is unable to promote apoptosis, suggesting that NFATc1/A enhances eff…

Gene isoformTranscription GeneticMolecular Sequence DataImmunologyApoptosisBiologyT-Lymphocytes RegulatoryJurkat CellsMiceExonAnimalsDeoxyribonuclease IHomeostasisHumansImmunology and AllergyPromoter Regions GeneticTranscription factorMice Inbred BALB CBase SequenceNFATC Transcription Factorsintegumentary systemEffectorNuclear ProteinsNFATDNA MethylationMolecular biologyChromatinDNA-Binding ProteinsAlternative SplicingInfectious DiseasesCpG siteApoptosisElectrophoresis Polyacrylamide GelPoly ATranscription FactorsImmunity
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