Search results for "Reaction"

Noncanonical RNAs from transcripts of the Drosophila muscleblind gene.

2006

It has become increasingly evident that eukaryotic cells produce RNA molecules from coding genes with constitutions other than those of typically spliced mRNA transcripts. Here we describe new cDNAs from the Drosophila melanogaster muscleblind (mbl ) locus that identify two such atypical RNA molecules: RNAs containing an incomplete exon 2 tandem repetition (mblE2E2#) or having exons with a different order compared to the corresponding genomic DNA (mblE2E3#E2#; exon scrambling). The existence of exon duplications and rearrangements in the genomic locus that might explain such cDNAs was ruled out by genomic Southern blotting and in silico analysis of the Drosophila genome sequence. The incomp…

Highly selective and sensitive chromo-fluorogenic detection of the Tetryl explosive using functional silica nanoparticles

2011

Silica nanoparticles containing polyamines and thiol groups have been used as probes for the selective detection of Tetryl. © 2011 The Royal Society of Chemistry.

Effect of adding new phosphazene compounds to poly(butylene terephthalate)/polyamide blends. I: Preliminary study in a batch mixer

2005

Abstract Poly(butylene terephthalate) (PBT) and a sample of polyamide have been melt processed in the presence of two new phosphazene compounds, namely 2,2-dichloro-4,4,6,6-bis[spiro(2′,2″dioxy-1′,1″biphenyl)]cyclotriphosphazene (2Cl-CP) and 2,2-bis-(2-methoxy-4-methyleneoxy-phenoxy)-4,4,6,6,-bis[spiro(2′,2″dioxy-1′,1″biphenyl)]cyclophosphazene (CP-2EPOX). The blends were prepared by using polyamide 6 (PA6) at 25/75 w/w and 75/25 w/w composition. In order to perform a preliminary analysis on the behaviour of the blends, the materials were prepared in a batch mixer. The materials have been completely characterized from a rheological, morphological, mechanical point of view. The results indic…

Indirect Catalytic Spectrophotometric Determination of Metamizol Following Oxidation by Lead Dioxide Immobilized in A Polyester Resin Bed

1996

Abstract A spectrophotometric-indirect procedure for the determination of metamizol is described. The method is based on the reaction of the drug in a solid-phase (lead dioxide immobilized in a polyester resin bed) in acidic media (perchloric acid 0.01 M as carrier). The lead dioxide reactor provides simultaneously an effective oxidation of the drug and a controlled liberation of Pb(II) which acts as catalyst on the reaction pyrogallol red-potassium persulphate; the oxidation of the red pyrogallol results in a less coloured solution. The decreased red colour (negative FIA peaks) is monitored at 520 nm. The calibration graph is linear in the interval 2–16 ppm in metamizol. The relative stand…

Is real-time PCR more useful than a conventional PCR for the clinical management of leishmaniasis?

2009

It is currently unknown if the use of a real-time polymerase chain reaction (PCR) adds value to the diagnosis and follow-up prognosis of patients affected by leishmaniasis. We performed a study using a real-time PCR directed against the α-polymerase gene and a semiquantitative PCR that target the SSU ribosomal RNA (rRNA) gene as control for the diagnosis and quantification of parasites in patients with visceral (VL) and cutaneous (CL) leishmaniasis. Our single copy real-time PCR missed one diagnosis of VL compared with the conventional PCR, whereas both PCR methods were able to detect Leishmania parasites in CL. Under anti-leishmania treatment the kinetics of parasitemia were comparable wit…

Polymerase Chain Reaction (PCR)

2008

Blends of polyamide 6 and bisphenol-A polycarbonate. Effects of interchange reactions on morphology and mechanical properties

1992

Blends of polyamide 6 (PA6) and polycarbonate (PC) were prepared in a Brabender mixer, at 240°C, applying long mixing time, for 45 min. It was observed that the morphology and the mechanical properties tend to resemble those of a homogeneous material as the mixing time and PA6 concentration increase. This is attributed to chemical reactions taking place between the two homopolymers. Acidolysis, amidolysis, and aminolysis, catalyzed by the terminals and the amide groups of the polyamide, should in principle be possible. Our results indicate that the aminolysis is the main process, inducing simultaneously scission of PC chains and formation of PC-PA6 copolymer chains. The latter act as interf…

Racemic S ‐(ethylsulfonyl)‐ dl ‐cysteine N ‐Carboxyanhydrides Improve Chain Lengths and Monomer Conversion for β‐Sheet‐Controlled Ring‐Opening Polyme…

2020

The secondary structure formation of polypeptides not only governs folding and solution self-assembly but also affects the nucleophilic ring-opening polymerization of alpha-amino acid-N-carboxyanhydrides (NCAs). Whereby helical structures are known to enhance polymerization rates, beta-sheet-like assemblies reduce the propagation rate or may even terminate chain growth by precipitation or gelation. To overcome these unfavorable properties, racemic mixtures of NCAs can be applied. In this work, racemicS-(ethylsulfonyl)-dl-cysteine NCA is investigated for the synthesis of polypeptides, diblock and triblock copolypept(o)ides. In contrast to the polymerization of stereoregularS-(ethylsulfonyl)-…

Polymerization of Triazolinediones withtrans-3,3-Dichloro-1-phenyl-1-propene

1997

The reaction of 4-phenyl-1,2,4-triazoline-3,5-dione (PhTD) (2) with trans-3,3-dichloro-1-phenyl-1-propene (4) was investigated at room and reflux temperatures in methylene chloride solution. Although the reaction is slow, it gives quantitative yield. This reaction leads to the formation of two 2:1 adducts via double Diels–Alder and Diels–Alder-Ene reactions in a ratio of about 1: 7. The major product was isolated by means of fractional crystallization as a pure compound and was characterized by infra-red (IR), 1H nuclear magnetic resonance (NMR), 13C NMR, mass spectra and elemental analysis. The structure of the minor product was determined by IR and 1H NMR. These compounds were used as mod…

FTIR isothermal cure kinetics and morphology of dicyanate ester resin/polysulfone blends

2005

Abstract The isothermal cure of a dicyanate ester monomer by “in situ” Fourier transform infrared spectroscopy (FTIR) has been investigated. The degree of cyanate conversion and the kinetic parameters have been determined for cobalt catalyzed and uncatalyzed resin as well as for polysulfone (PSF) modified systems at different curing temperatures. The cyanate conversion increases with the increment of temperature and with the addition of a catalyst, but it does not vary with the addition of PSF. In all the systems studied, the rate of reaction showed a second-order dependence on the cyanate concentration in the kinetically controlled stage. Moreover, the addition of PSF generates a matrix wi…