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  • Using ultrapure water in ion chromatography to run analyses at the ng/L level 15250398

    Thanks to enhanced capabilities, ion chromatography (IC) occupies an increasing position in many types of applications. Achieving ideal performances for an extended life-time can only be reached, however, if the IC system is operated in optimum experimental conditions. Among the various parameters that need to be controlled, water is particularly important, because it is used throughout the analysis, from sample preparation to column rinsing, elution, and mobile phase preparation. More and more, devices are included in IC systems to generate the eluent in situ, and ultrapure water becomes the major reagent. Data of pre-concentration of high purity water show that detection limits at the ng/L level can be expected with water purified using the right combination of technologies.
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    Referencia del producto:
    Múltiplo
    Nombre del producto:
    Múltiplo

  • Using ultrapure water in ion chromatography to run analyses at the ng/L level 15250398

    Thanks to enhanced capabilities, ion chromatography (IC) occupies an increasing position in many types of applications. Achieving ideal performances for an extended life-time can only be reached, however, if the IC system is operated in optimum experimental conditions. Among the various parameters that need to be controlled, water is particularly important, because it is used throughout the analysis, from sample preparation to column rinsing, elution, and mobile phase preparation. More and more, devices are included in IC systems to generate the eluent in situ, and ultrapure water becomes the major reagent. Data of pre-concentration of high purity water show that detection limits at the ng/L level can be expected with water purified using the right combination of technologies.
    Tipo de documento:
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    Referencia del producto:
    Múltiplo

  • Plasma and urinary oxalate and glycolate in healthy subjects. 8419038

    High-performance ion chromatography (HPIC) has been widely used for oxalate analysis and, more recently, for glycolate analysis. We describe a procedure for sample preparation in which the plasma ultrafiltrate is acidified during harvesting with a cation-exchange resin, and the chloride is removed before the ion chromatography, which is performed with a newly developed AS10 column. The same ultrafiltrate sample is analyzed for glycolate. For plasma oxalate, the mean recovery of sample in eluted fractions was 95-96%, and intraassay CV was 6.2-8.1%. The reference interval (mean +/- 2 SD) for men was 0.8-3.2 mumol/L and for women, 1.0-2.6 mumol/L. For urinary oxalate, the reference interval for men was 175-560 mumol/day and for women, 107-432 mumol/day. For plasma glycolate, the mean analytical recovery was 96-98%, and the intra-assay CV was 2.4-6.2%. The reference interval for men was 1.9-7.5 mumol/L and for women, 1.4-7.4 mumol/L. For urinary glycolate, the reference interval for men was 0-1400 mumol/day and for women, 91-1001 mumol/day.
    Tipo de documento:
    Referencia
    Referencia del producto:
    20-176
    Nombre del producto:
    100X GTPγS, 10mM

  • Impact of purified water quality on molecular biology experiments. 12747591

    Purified water is a reagent used in a variety of molecular biology experiments, for sample and media preparation, in mobile phases of liquid chromatography techniques, and in rinsing steps. The combination of several technologies in water purification systems allows delivering high-purity water adapted to each application and technique. Through a series of examples, the importance of water quality on biotechnology experiments, such as single nucleotide polymorphism (SNP) analysis by denaturating HPLC, RNA preparation and PCR, is presented. Results obtained on DNA mutation and single nucleotide polymorphism analysis using the denaturating HPLC (DHPLC) technique highlight the benefits of organic removal by UV photooxidation process. Comparative gel electrophoresis data show that ultrafiltration is as efficient as diethylpyrocarbonate (DEPC) treatment for suppressing RNase activity in water. Gel electrophoresis and densitometry measurement also point out the benefits of ultrafiltration to carry out reverse transcriptase-polymerase chain reaction quantitatively.
    Tipo de documento:
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    Referencia del producto:
    Múltiplo
    Nombre del producto:
    Múltiplo

  • Analysis of 8-methoxypsoralen by high-performance liquid chromatography. 2242576

    We report a simple and rapid procedure for assaying 8-methoxypsoralen (8-MOP) in plasma by high-performance liquid chromatography (HPLC). The standard curve for the assay is linear for 8-MOP from 15 to 500 micrograms/L (y = 0.002x-0.01, r = 0.99) with a lower limit of detection of 1.5 micrograms/L. Intra-assay precision (CV) was 6.0% at the 100 micrograms/L concentration and 10.0% at 50 micrograms/L (n = 30 each). Interassay precision was 6.4% at 100 micrograms/L and 7.0% at 50 micrograms/L (n = 50 each). Extraction recovery of 8-MOP was 98%. Common antiarrhythmics, sedatives, and hypnotics were found not to interfere.
    Tipo de documento:
    Referencia
    Referencia del producto:
    20-176
    Nombre del producto:
    100X GTPγS, 10mM

  • Rapid detection of the addition of soybean proteins to cheese and other dairy products by reversed-phase perfusion chromatography 16546880

    The undeclared addition of soybean proteins to milk products is forbidden and a method is needed for food control and enforcement. This paper reports the development of a chromatographic method for routine analysis enabling the detection of the addition of soybean proteins to dairy products. A perfusion chromatography column and a linear binary gradient of acetonitrile-water-0.1% (v/v) trifluoroacetic acid at a temperature of 60 C were used. A very simple sample treatment consisting of mixing the sample with a suitable solvent (Milli-Q water or bicarbonate buffer (pH¼11)) and centrifuging was used. The method enabled the separation of soybean proteins from milk proteins in less than 4 min (at a flow-rate of 3 ml/min). The method has been successfully applied to the detection of soybean proteins in milk, cheese, yogurt, and enteral formula. The correct quantitation of these vegetable proteins has also been possible in milk adulterated at origin with known sources of soybean proteins. The application of the method to samples adulterated at origin also leads to interesting conclusions as to the effect of the processing conditions used for the preparation of each dairy product on the determination of soybean proteins.
    Tipo de documento:
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    Referencia del producto:
    Múltiplo

  • A total water purification system A total water purification system

    Many of the analytical and molecular biology applications that require the use of water include high-performance liquid chromatography (HPLC), total organic carbon (TOC) analysis, sample and media preparation, rinse steps in assays, and gel electrophoresis. Different types of laboratories run experiments that require varying levels of water purity. What is needed in one lab might not be needed in another. Therefore, professional organizations have established water quality standards or guidelines to facilitate laboratory water purification within various industry sectors
    Tipo de documento:
    Referencia
    Referencia del producto:
    Múltiplo
    Nombre del producto:
    Múltiplo

  • Urinary metanephrine and normetanephrine determined without extraction by using liquid chromatography and coulometric array detection. 8375055

    We describe a procedure for the direct measurement of metanephrine (MN) and normetanephrine (NMN) in hydrolyzed urine, using HPLC with coulometric array detection. Acid-hydrolyzed samples were diluted and filtered before separation by isocratic reversed-phase ion-pair chromatography. Eight serial coulometric sensors, set at incrementally increasing anodic potentials, were used to screen lower-oxidizing interferences and provide stepwise oxidation of the metanephrines. Voltammetric behavior across three adjacent sensors was used to assess resolution and aid in peak identification. Values obtained in commercial controls were consistently within the specified target range. Variability, expressed as CV, was 5.45-9.22% between runs and 1.60-4.52% within-run for both compounds. The limit of detection was 2.6 micrograms/L for MN and 2.8 micrograms/L for NMN, with a linear response to 15.0 mg/L for both analytes. Results from patients' samples correlated well with those by a method involving dual ion-exchange extraction (r = 0.963, n = 82 for MN; r = 0.9768, n = 83 for NMN). This procedure provided high selectivity and objective peak purity information while greatly simplifying sample preparation.
    Tipo de documento:
    Referencia
    Referencia del producto:
    20-176
    Nombre del producto:
    100X GTPγS, 10mM

  • Homocysteine and other thiols determined in plasma by HPLC and thiol-specific postcolumn derivatization. 8353942

    We describe a versatile high-performance liquid-chromatographic method for determining homocysteine and other plasma sulfhydryls. Using three different procedures for preparation of plasma, we determined total, free (non-protein-bound), and reduced forms of homocysteine, cysteine, glutathione, cysteinylglycine, and gamma-glutamylcysteine in human plasma. Sample preparation involves disulfide reduction with dithiothreitol and protein precipitation with sulfosalicylic acid. The assay utilizes isocratic reversed-phase ion-pair liquid chromatography at pH 2.4, postcolumn derivatization with 4,4'-dithiodipyridine, and colorimetric detection at 324 nm. The intra-assay precision (CV) of the method for total homocysteine is 1.5%; the interassay precision over 2.5 months is 2.5%. The detection limit for homocysteine is < 50 nmol/L plasma.
    Tipo de documento:
    Referencia
    Referencia del producto:
    20-176
    Nombre del producto:
    100X GTPγS, 10mM