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    Biochem. J. (1995) 305‚ 17-20 (Printed in Great Britain) 17 RESEARCH COMMUNICATION The effect of low temperatures Nicole MORE‚ Roy M. DANIEL* and Helen H. PETACH on enzyme activity Thermophile Research Unit‚ University of Waikato‚ Private Bag 3105‚ Hamilton 2001‚ New Zealand The stability of two enzymes from extreme thermophiles (glutamate dehydrogenase from Thermococcales strain ANI and f‚- enzymes‚ glucosidase from Caldocellum saccharolyticum expressed in Escherichia

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    Porcine Skin

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    Analyst Cite this: Analyst‚ 2011‚ 136‚ 2359 www.rsc.org/analyst View Article Online / Journal Homepage / Table of Contents for this issue Dynamic Article Links < C PAPER Characterization of porcine skin as a model for human skin studies using infrared spectroscopic imaging Rong Kong and Rohit Bhargava* Downloaded by Queen Mary‚ University of London on 19/04/2013 18:44:34. Published on 21 April 2011 on http://pubs.rsc.org | doi:10.1039/C1AN15111H Received 10th February 2011‚ Accepted

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    3.1 Overview The experiment was divided into three parts. In the first part was the preparation of empty CNPs. The second part was the preparation of CNPs loaded with single drug which was AA and TQ meanwhile the third part was the preparation of CNPs loaded with dual drug (AA and TQ). The last part was the analytical testing conducted to investigate the properties performance such as smaller or larger in trend as well as to characterize the entrapment efficiency of drugs. The chemicals and technique

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    swab stick was dipped into the test tube containing the organisms and it was used to seed the organism on the solidified Muella Hinton agar. The prepared disc was transferred on the the inoculated culture plates. The placed disc included 100mg/ml (DMSO) and gentamycin 2mg/ml.The plates were incubated for 24hours at 37oC‚ after which the zone of inhibition was measured and recorded. The test was carried out in duplicate. | 10. Analysis of data (results). What are the statistical tools used? |

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    Introduction Chemists often find a method to determine the level of “greenness” of a chemical reaction‚ or its “atom economy”. A higher atom economy is preferable because a greater amount of the reactants will be present in the product as opposed to the byproduct.1 A Suzuki reaction is classified as an organic‚ coupling reaction that includes boronic acid and a halide that are catalyzed by a palladium complex under basic conditions. Other palladium- catalyzed coupling mechanisms include the Heck

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    INTRODUCTION Cassia fistula Linn. (Leguminosae) is a very common plant and is widely known for its medicinal properties. In the Indian literature‚ this plant has been described to be useful against skin diseases‚ liver troubles‚ tuberculous glands and its use in the treatment of rheumatism‚ hematemesis‚ pruritus‚ leucoderma‚ and diabetes.[1‚2] Besides‚ it has been found to exhibit anti-inflammatory and hypoglycemic activity and widely used as a mild laxative suitable for children and pregnant women

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    3 Perylenepentanon

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    M5 (4.54 g‚ 17.2 mmol) and sodium 6-oxidonaphalene-2-sulfonate (0.84 g‚ 3.13 mmol) were dissolved in 30 ml of DMSO. The mixture was stirred at room temperature overnight. The mixture was poured into ice cold acetone with continuous stirring. The mixture was filtered and washed with DCM and methanol to yield the title compound as pale yellow solid. Yield (0.13 g‚ 9 %). δH (400 MHz‚ DMSO-d6) 3.83 (2 H‚ s‚ CH2Br)‚ 5.25 (2 H‚ s‚ CH2OAr)‚ 7.25-7.26 (1 H‚ br d‚ J = 6.36 Hz‚ 3-ArH)‚ 7.30-7.50 (2 H‚ m‚

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    is produced by CHCl3 and 1.74g γ-mangostin from CHCl3-MeOH. A reversed-phase HPLC is done to determine the purity (98.0%) for each compound. In preparing the samples‚ test solutions of xanthone (20mg/ml) were prepared by dissolving each compound in DMSO. The test solutions were kept at 4oC until

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    Experimental Synthesis of Bupropion – A round bottom flask (RBF) containing m-chloropropiophenone (1.0 g‚ 5.9 mmol) dissolved in 5.0 mL dichloromethane (DCM) with 0.25 mL of 1.0 M Br2 in DCM was briefly warmed to initiate the bromination reaction. Afterwards‚ the RBF was placed in and ice-water bath and 1.0 M Br2 in DCM (6.0 mL‚ 6.25 mmol) was added dropwise while stirring. DCM was removed from the reaction by rotary evaporation. Next‚ tert-butylamine (5.0 mL‚ 47.6 mmol) and 5.0 mL of N-methylpyrrolidinone

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    22.12.2009 EN Official Journal of the European Union L 342/59 REGULATION (EC) No 1223/2009 OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL of 30 November 2009 on cosmetic products (recast) (Text with EEA relevance) THE EUROPEAN PARLIAMENT AND THE COUNCIL OF THE EURO­ PEAN UNION‚ (5) Having regard to the Treaty establishing the European Commu­ nity‚ and in particular Article 95 thereof‚ Having regard to the proposal from the Commission‚ Having regard to the opinion of the European Economic

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