Search results for "Blood Protein"

showing 10 items of 175 documents

Mobility of Acetylated Histones in Sodium Dodecyl Sulfate–Polyacrylamide Gel Electrophoresis

1999

Abstract We describe an altered mobility for acetylated histone isoforms in sodium dodecyl sulfate–polyacrylamide gel electrophoresis. Isoforms of histones H3 and H4 with a higher acetylation degree have a slightly faster electrophoretic mobility. Since acetylation neutralizes the positive charge of the e-amino group of lysine, without significantly changing the molecular mass of the protein, the acetylation-dependent mobility shift could be explained by the increase of the net negative charge of the SDS–histone complexes. A possible consequence of this differential mobility for the acetylation site determination by protein microsequencing from SDS gels is discussed.

ErythrocytesSodiumLysineBiophysicschemistry.chemical_elementBiochemistryHistoneschemistry.chemical_compoundElectrochemistryAnimalsSodium dodecyl sulfateMolecular BiologyPolyacrylamide gel electrophoresisGel electrophoresisChromatographyMolecular massReproducibility of ResultsSodium Dodecyl SulfateAcetylationCell BiologyBlood Protein ElectrophoresisElectrophoresischemistryBiochemistryAcetylationElectrophoresis Polyacrylamide GelChickensAnalytical Biochemistry
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In vivo survival rate of rabbit morulae after vitrification in a medium without serum protein.

2000

The in vivo survival rate of rabbit morulae after vitrification in a mixture of dimethyl sulphoxide and ethylene glycol solution without protein supplement (WPS) was compared with two types of protein supplements: rabbit serum (RS) and bovine serum albumin (BSA). Significant dif- ferences were observed in the percentage of transferable embryos (undamaged embryos after devit- rification, 80.4 % versus 93.2 and 92.1 %, WPS, BSA and RS, respectively, P < 0.05) and live born rate (40.9 % versus 56.1 %, WPS and BSA, respectively, P < 0.05). Non-significant differences were, however, observed in the percentages of implanted embryos at 12 days post-ovulation induc- tion (56.7, 69.7 and 68.6 %), po…

Ethylene GlycolMorulaAndrologychemistry.chemical_compoundCryoprotective AgentsPregnancyIn vivo[SDV.BDD] Life Sciences [q-bio]/Development BiologyAnimalsDimethyl SulfoxideVitrificationEmbryo ImplantationBovine serum albuminFetal DeathSurvival rate[SDV.BDLR] Life Sciences [q-bio]/Reproductive BiologyCryopreservationLagomorphabiologySerum Albumin BovineEmbryo cultureBlood ProteinsEmbryo Transferbiology.organism_classificationEmbryo transfer[SDV.AEN] Life Sciences [q-bio]/Food and NutritionBloodchemistryBiochemistrybiology.proteinFemaleRabbitsEthylene glycol
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Data concerning the protein absorption and retention properties of xyloglucan-based hydrogel film

2018

In wound dressing applications, exudate absorption and retention are important properties. The data presented here assess the ability of the crosslinked xyloglucan-poly(vinyl alcohol) hydrogel films (XG-PVA), described in "Xyloglucan-based hydrogel films for wound dressing: Structure-property relationships" (Ajovalasit et al., 2018) [1] and "Biocompatibility, hemocompatibility and antimicrobial properties of xyloglucan-based hydrogel film for wound healing application" (Picone et al., 2019), to absorb and retain proteins. These properties were investigated by Comassie blue staining and electrophoresis of Fetal Serum Proteins. (C) 2018 The Authors. Published by Elsevier Inc. This is an open …

Exudateprotein retentionVinyl alcoholBiocompatibilitymacromolecular substances02 engineering and technologyAbsorption (skin)lcsh:Computer applications to medicine. Medical informatics010402 general chemistry01 natural scienceschemistry.chemical_compoundbiocompatibilitymedicinelcsh:Science (General)Multidisciplinaryintegumentary systemprotein absorptionChemistrytechnology industry and agricultureChemical Engineering021001 nanoscience & nanotechnologyBiomaterialBlood proteins0104 chemical sciencesXyloglucanElectrophoresisChemical engineeringlcsh:R858-859.7Settore CHIM/07 - Fondamenti Chimici Delle Tecnologiemedicine.symptom0210 nano-technologyWound healinglcsh:Q1-390
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Reference Typing Reportfor Complement Component C3

1998

A comparison of five C3 variant samples has been performed by conventional high-voltage gel electrophoresis in three laboratories (Palermo, Berlin and Mainz). Local designation was shown within SD = ±0.75 mm migration distance in the Mainz laboratory. Methodological modifications by laboratories were not accounted for (cooling temperature, relative mobilities between runs). In parallel, all reference samples were also sequenced after exon-specific amplification. As a result, two variants with identical final designations and two variants with different mobilities were shown to conform at the molecular basis exhibiting an amino acid exchange that causes the corresponding change in relative m…

Gel electrophoresisChemistryComponent (thermodynamics)C3 polymorphismCooling temperatureImmunologyAnalytical chemistryMolecular biologyhumanitiesBlood protein electrophoresisGeneticsTypingReference standardsGenetics (clinical)Complement (set theory)Experimental and Clinical Immunogenetics
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Screening for multiple hereditary hypercoagulability factors using the amplification refractory mutation system

2003

Many hereditary factors have been implicated in the development of arterial and/or venous thromboembolic diseases. A number of these risk factors can be identified by the amplification refractory mutation system (ARMS). However, the underlying technical conditions for performing ARMS are highly variable, and depend on which risk factors are being analyzed. We have now developed a novel ARMS-based system to simultaneously screen for multiple hypercoagulability factors under identical PCR conditions. This can greatly simplify the process of screening for hereditary hypercoagulability.

GeneticsBase SequenceGenetic Carrier ScreeningHomozygoteGenetic Carrier ScreeningSingle-strand conformation polymorphismBlood ProteinsHematologyBlood Coagulation DisordersBiologymedicine.diseaseThrombophiliaBioinformaticsPolymerase Chain ReactionThrombosisBlood Coagulation FactorsRefractoryMutation (genetic algorithm)medicineCoagulopathyHumansMass ScreeningRisk factorDNA PrimersThrombosis Research
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Accelerated Evolution of Fetuin-A (FETUA, also AHSG) is Driven by Positive Darwinian Selection, not GC-Biased Gene Conversion

2009

article i nfo Human Fetuin-A (FETUA, also termed AHSG) is a serum protein composed of two cystatin-like domains D1 and D2 of together 235 amino acids (aa) and an unrelated domain D3 of 114 aa. Though the protein plays a role in diverse physiological and pathological processes, comparably little is known about sequence evolution of FETUA. We therefore analyzed its molecular evolution on the basis of coding sequences of 16 primate species. Ratios of non-synonymous to synonymous substitution rates (dn/ds= ω) suggest that a previously reported acceleration of sequence evolution of exon 7, which encodes domain D3, is driven by positive selection instead of neutral evolution. Irrespective of the …

GeneticsBase Sequencealpha-2-HS-GlycoproteinNull modelGene ConversionLocus (genetics)Blood ProteinsGeneral MedicineBiologyCleavage (embryo)Protein Structure TertiaryEvolution MolecularExonMolecular evolutionGeneticsAnimalsHumansGene conversionSelection GeneticCodonSynonymous substitutionNeutral theory of molecular evolutionGene
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Results of collaborative study regarding the standardization of the Y-linked STR system DYS385 by the European DNA Profiling (EDNAP) group.

1999

Y-chromosome linked short tandem repeat (STR) loci are inherited as a closely linked haplotype, which appears to remain stable in a given paternal lineage over many generations. In forensic cases, Y-linked STRs are particularly useful for the identification of human remains as well as in rape cases with mixed male/female stain samples. DYS385 is derived from tandemly duplicated segments of the Y chromosome thus giving rise to two fragments of variable length which do not behave like alleles but genotypes. The European DNA Profiling (EDNAP) group has carried out a collaborative exercise among 14 participating laboratories using DYS385 for typing of five unknown bloodstains and a control samp…

GeneticsMaleGenetic LinkageSTR multiplex systemInternational CooperationHaplotypeReproducibility of ResultsMinisatellite RepeatsBiologyY chromosomeBlood Protein ElectrophoresisDNA FingerprintingPathology and Forensic MedicineEuropeGenetics PopulationDNA profilingBlood StainsY ChromosomeGenotypeY linkageMicrosatelliteHumansTypingLawForensic science international
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Serumprotein polymorphisms in Iran.

1968

The results of a population genetic investigation on Iranians are given and compared to the results obtained on other populations from Southwestern and Southern Asia. Our total material from Iran comprises n=1020 nonrelated male and female individuals of different age. The following serum groups have been typed: Hp, Gc, Gm, and Inv. In general there exist no remarkable age or sex differences in the distribution of phenotypes and alleles (the only exception: sex differences in the distribution of the Gm (7)-phenotype). The regional distribution of phenotypes and alleles yield no marked differences, too, apart from the Invphenotypes, however. For the total material of Iran the following allel…

GeneticsMaleeducation.field_of_studyPolymorphism GeneticPopulationBlood ProteinsBiologyIranPhenotypeGene FrequencyPolymorphism (computer science)GeneticsHumansFemaleAlleleeducationAllele frequencyGenetics (clinical)Humangenetik
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Application of liquid-liquid partition chromatography in the simultaneous purification of sex-hormone-binding globulin and corticosteroid-binding glo…

1987

Two human serum proteins, corticosteroid-binding globulin (CBG) and sex-hormone-binding globulin (SHBG), were purified to homogeneity by the application of a combination of three different modes of chromatography. Human pregnancy serum was fractionated with ammonium sulphate. SHBG (50% pellet) and CBG (80% pellet) were then purified by affinity chromatography on tresyl-activated Sepharose with 15-aminopentadecanoic acid (for SHBG) and 1,12-diaminododecane (for CBG) as spacers and 17 zeta-aminoethyl-5 alpha-androstan-3 beta,17-diol (for SHBG) and 17 alpha-hydroxy-4-androsten-3-one-17 beta-carboxylic acid (for CBG) as specific ligands for these two proteins. The eluate was injected into a Mon…

GlobulinSerum albuminReceptors Cell SurfaceBiochemistryChromatography AffinityAnalytical ChemistrySepharoseSex hormone-binding globulinTranscortinAffinity chromatographyPregnancySex Hormone-Binding Globulinpolycyclic compoundsHumansreproductive and urinary physiologyTranscortinChromatographybiologyChemistryElutionOrganic ChemistryGeneral MedicineBlood proteinsBiochemistrybiology.proteinElectrophoresis Polyacrylamide GelFemaleSpectrophotometry UltravioletIsoelectric Focusinghormones hormone substitutes and hormone antagonistsChromatography LiquidJournal of chromatography
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Quantitative Bestimmung des Gallenr�ckflusses in Blut und Leberlymphe von Ratten bei beginnender Gallenstauung

1970

1. Mit dem Ziel, die Anteile des bei einer Gallenstauung auftretenden Gallenruckflusses in Blut und Lymphe quantitativ zu erfassen, wurde ein Verfahren zur Gewinnung reiner Leberlymphe bei Ratten entwickelt. 2. Mit Hilfe dieser Methode konnte am Versuchstier mit normaler Korpertemperatur aus Messungen der Lymphstromstarke und des Eiweisgehaltes der Leberlymphe vor und wahrend einer Gallenstauung auf einen Ruckflus der fortlaufenden produzierten Galle in die Leberlymphe von ca. 7–10% geschlossen werden. 3. In Ruckflusversuchen an unterkuhlten Ratten mit Ringerlosung, die Evansblue enthielt, ergaben Analysen von Blut und Leberlymphe einen Anteil des Ruckflusses in diese Lymphe von ca. 13%.

GlobulinbiologyPhysiologybusiness.industryClinical BiochemistrySerum albuminRegurgitation (circulation)medicine.diseaseMolecular biologyBlood proteinsQuantitative determinationCholestasisPhysiology (medical)medicinebiology.proteinLymphbusinessBlood streamPfl�gers Archiv European Journal of Physiology
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