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Just as Visual Basic® sparked a wave of innovation in business applications and made the PC an essential business tool, Visual Studio .NET 2003 and the .NET Compact Framework will unlock the potential of Web services and rich data on smart devices. This will enable developers to drive a new era of innovation in the mobile marketplace, transforming smart devices into must-have productivity tools. The .NET Framework and the .NET Compact Framework provide a consistent programming model across the full range of Windows platforms and expose that programming model through a single unified tool set, Visual Studio .NET 2003. Together, Visual Studio .NET 2003 and the .NET Compact Framework enable millions of desktop Visual Basic developers and the rapidly growing market of C# developers to begin building smart mobile applications. Features of the .NET Compact Framework and Visual Studio .NET 2003 include support for XML and Web services; the ability to integrate components written in multiple ...

Table salt could be used to increase the capacity of hard drives from as much as 4 Tbytes today to more than 21 Tbytes, according to researchers at the Institute of Materials Research and Engineering (IMRE). The method involves the use of a very high-resolution e-beam lithography, which is the process used to create fine nanoscale circuitry. The researchers added sodium chloride to a developer solution used in lithography processes and were able to produce highly defined nanostructures that were as small as 4.5 nm, without using expensive equipment upgrades. IMREs Joel Yang developed the salty developer solution, and worked with researchers at the National University of Singapore and the Data Storage Institute to perfect the nanopatterning technique. What we have shown is that bits can be patterned more densely together by reducing the number of processing steps, Yang says. The teams packages of bits deposited on the surface of a platter are about 10 nm in size. The researchers hope to ...

A method and device for determining the presence of an analyte in a sample suspected of containing the analyte is disclosed. The method involves contacting a test solution containing the sample and a first member of a specific binding pair with an end portion of a strip of bibulous material capable of being traversed by the test solution through capillary action. The first member of a specific binding pair is capable of binding the analyte. The strip contains a second member of a specific binding pair integral therewith for concentrating and non-diffusively binding the first sbp member at a small situs on the strip separated from the end portion of the strip. The detectible signal is produced in relation to the presence of the analyte in the test solution. The test solution passes through the situs as the test solution traverses the bibulous material. After the test solution has been allowed to traverse at least a portion of the strip, the strip is contacted with a developer solution containing members

The asymmetric hetero-Diels-Alder (HDA) reaction is among the most powerful available methodologies for the construction of optically active six-membered heterocycles, with extensive synthetic applications in natural or unnatural products with a wide range of biological activity. The DA reaction has high regioselectivity and endo-stereoselectivity. This Highlight reviews recent developments from 2005 to present (for comprehensive reviews on asymmetric DA reaction see a) Angew. Chem. Int. Ed. 2002, 41, 1650. ; b)Angew. Chem. Int. Ed. 2002, 41, 1668. ; c) Mini-Reviews in Organic Chemistry, 2004, 1, 41. Link). Some of the examples presented here use organocatalysis, which is a rapidly growing research field.. ...

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a) Fixer (10% acetic acid) Add 50 ml glacial acetic acid to 450 ml distilled water b) Silver stain Add 3 ml 1N silver nitrate solution in 500 ml distilled water. Then add 0.75ml formamide c) Developer Dissolve 15 g sodium carbonate in 500 ml distilled water and put at 4 O C 1. Remove the gel and separate the plates carefully with a single-edged razor blade. 2. Place the gel in tray with the fixer and leave shaking in a fume hood for 30 minutes. Pour off fixer (save). 3. Wash with water for 10 15 minutes, on shaker. Rinse again and pour off the water. 4. Add silver-stain and leave shaking for 30 minutes (Silver stain can be re-used up to 10 times). 5. Immediately before developing the gel, add in 75 m l sodium thiosulphate solution (0.1N) and 0.75 ml formamide to the pre-chilled developer solution. 6. After silver-stain (step 4), agitate the gel several times for 10 seconds. 7. Immediately agitate the gel in the developer until band development progress sufficiently. 8. Stop the reaction by ...

Dear HistoNetters Happy Holidays! Heres a nice microwave version of the Bodian Stain, courtesy of Dr. Mathilde Boon: The Bodian silver stain is used to color neurofibrils, unmyelinated and myelinated nerve fibers. SOLUTIONS NEEDED: Protargol solution: 0.5 g Protargol 3.0 g Metallic Copper Shot 50 ml Distilled water NOTE: Prepare the solution immediately before use. Developer solution: 1 g Hydroquinone (C6H6O2) 50 ml Distilled water 2.5 ml 37% formalin (CH2O) NOTE: Prepare the solution immediately before use. Gold Chloride solution: 1 g Gold (III) Chloride (HAuCl4 H2O, 49% pure) 100 ml Distilled water 3 drops Glacial Acetic acid Oxalic Acid solution: 1 g Oxalic acid dihydrate (C2H2O4 2H2O) 50 ml Distilled water Sodium Thiosulfate solution: 5 g Sodium Thiosulfate (Na2S2O3 5H2O) 50 ml Distilled water PROCEDURE: 1. Deparaffinize and bring to water 2. 60 min / 37 C in conventional incubation / 50 ml of Protargol solution 3. 60 min / 60 C / same Protargol solution 4. Rinse well in distilled water 5. ...

To understand, how hair dyes work - you first need to know about the hair anatomy.. Hair comprises of three layers - medulla, cortex, and cuticle.. The core layer is called the medulla.. Cortex is surrounded by a thick layer of cells. It is responsible for pigmentation and melanin.. The cuticle is the outer layer that protects your hair.. Along with hair anatomy, you also need to know three types of hair dye - temporary, semi-permanent, and permanent hair dye.. When you apply temporary hair dye, it will just stick to the outer layer of the hair, i.e. cuticle. Due to it, the colour will vanish instantly after shampooing.. Whereas semi-permanent hair dye contains molecules that can slip between the cuticle and can stick to the cortex. As a result, it wont vanish easily even after shampooing. It will last for about 12 shampoos.. Permanent hair dye stays with your hair until it grows and falls out.. It contains two solutions alkaline and developers( Solution of hydrogen peroxide).. You mix both ...

4. Photographic Industries: It is mostly used in photographic industries for production of developer solution/acidizing fixation baths.. 5. Pulp and Textiles: It is used as a bleaching agent in pulp and textile industries.. 6. Rubber Industries: It is used as coagulative agnet for rubber industries.. 7. Acrylic Fibres : Chemical synthesis in manufacturing of Acrylic fibres and Acrylic sheets.. 8. Dye Industries : It acts as dechlorination agent in dye industries.. 9. Gold Mining Industries : It is used in Mining industries as floating agent ...

With the implementation of the Food and Drug Administrations Food Safety Modernization Act, the food industry must scientifically verify that current production processes provide sufficient protection against pathogens. This study was conducted to validate a simulated commercial baking process for hamburger buns to control Salmonella spp. contamination and to determine the appropriateness of using non-pathogenic surrogates (Enterococcus faecium ATCC 8459 or Saccharomyces cerevisiae) for in-plant process validation studies. Wheat flour was separately inoculated (~6 log CFU/g) with three Salmonella serovars (Typhimurium, Newport or Senftenberg) or E. faecium. Dough was formed, proofed, and baked to mimic commercial manufacturing conditions. Non-inoculated dough was used to evaluate S. cerevisiae (Bakers yeast) survival during baking. Buns were baked for 9, 11 and 13 min in a conventional oven set at 218°C, with internal bun temperature profiles recorded. Salmonella serovars and S. cerevisiae ...

A primary objective of this study was to characterize the budding of retroviruses in real time in vivo. Although entry of single HIV-1 particles has been imaged in live cells (19), we are not aware of similar studies on budding of single particles. We have shown that VLPs bud one at a time from the plasma membrane, occasionally from the same site. Correlated fluorescence microscopy and SEM imaging demonstrated that Gag-GFP can be incorporated into morphologically correct structures in the presence of excess untagged Gag and that a large fraction of the fluorescent spots observed by MPM correspond with properly assembled VLPs.. It has often been assumed that Gag-GFP properly carries out all of the functions of untagged Gag (4, 9-11, 15). Early evidence suggested that, by itself, RSV Gag-GFP formed particles with normal morphology (10). However, from more recent data (Rebecca Craven, personal communication), such particles seem to have heterogeneous sedimentation coefficients, consistent with the ...

The fluorescent two-hybrid assay (F2H) is a technique for the validation and characterization of protein-protein interactions in vivo. It can be used for studying the modulation of interactions with inhibitors or activators, for compound screening and for confirmation of results from other protein-protein interaction screens such as co-immunoprecipitation studies.. In short, two proteins, bait and prey protein, are fused to GFP and RFP, respectively. A BHK cell line is transformed with ChromoTeks F2H platform reagent and two DNA plasmids coding for the GFP-bait protein and the RFP-prey protein. The interaction of bait protein and prey protein can be detected by co-localization of a green and a red fluorescent spot in the nucleus of the BHK cells with an epi-fluorescence microscope.. PRODUCTS ...

The fluorescent two-hybrid assay (F2H) is a technique for the validation and characterization of protein-protein interactions in vivo. It can be used for studying the modulation of interactions with inhibitors or activators, for compound screening and for confirmation of results from other protein-protein interaction screens such as co-immunoprecipitation studies.. In short, two proteins, bait and prey protein, are fused to GFP and RFP, respectively. A BHK cell line is transformed with ChromoTeks F2H platform reagent and two DNA plasmids coding for the GFP-bait protein and the RFP-prey protein. The interaction of bait protein and prey protein can be detected by co-localization of a green and a red fluorescent spot in the nucleus of the BHK cells with an epi-fluorescence microscope.. PRODUCTS ...

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Consult a professional prior to cleaning. For ordinary cleaning, use mild soap and water. For more severe soiling, remove promptly with a non-abrasive cleaner. Gently lift any remaining spill to avoid further staining. Rub gently and rinse with water dampened cloth to remove cleaner concentration. Kindly spot test an area before cleaning. ...

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The IUPHAR/BPS Guide to Pharmacology. cephradine ligand page. Quantitative data and detailed annnotation of the targets of licensed and experimental drugs.

VOLVOCEF (Cephradine) is a first-generation cephalosporin antibacterial given orally and by parenteral route in the treatment of susceptible infections and

The information contained herein has been obtained from sources that the Company believes to be reliable, however, the Company has not independently verified or confirmed the information and the recipient acknowledges that no representations or warranties are being made in connection with the use of the information.. ...

Consult a professional prior to cleaning. For ordinary cleaning, use mild soap and water. For more severe soiling, remove promptly with a non-abrasive cleaner. Gently lift any remaining spill to avoid further staining. Rub gently and rinse with water dampened cloth to remove cleaner concentration. Kindly spot test an area before cleaning. ...

Pill with imprint biocraft 113 is Green, Capsule-shape and has been identified as Cephradine 500 MG. It is supplied by Teva Pharmaceuticals USA.

Purified Universal Kinase Fluorometric Assay Kit from Creative Biomart. Universal Kinase Fluorometric Assay Kit can be used for research.

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Enterococcus faecium ATCC ® 8459™ Designation: NCTC 2699 TypeStrain=False Application: Produces FAD flavin-adenine dinucleotide

Sodium Sulfide Spot Test Definition - A sodium sulfide spot test is a localized chemical test to detect any concentration of lead in a coating...

Quantitative microscopy deals with the extraction of quantitative measurements from samples observed under a microscope. Recent developments in microscopy systems, sample preparation and handling techniques have enabled high throughput biological experiments resulting in large amounts of image data, at biological scales ranging from subcellular structures such as fluorescently tagged nucleic acid sequences to whole organisms such as zebrafish embryos. Consequently, methods and algorithms for automated quantitative analysis of these images have become increasingly important. These methods range from traditional image analysis techniques to use of deep learning architectures.. Many biomedical microscopy assays result in fluorescent spots. Robust detection and precise localization of these spots are two important, albeit sometimes overlapping, areas for application of quantitative image analysis. We demonstrate the use of popular deep learning architectures for spot detection and compare them ...

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A method is provided to fluorometrically determine a ligand in an assay solution containing the ligand, reagent system and a fluorescer wherein the intensity of the fluorescer emitted by the assay sol

6-thio-dG induces persistent telomere damage in conjunction with extensive genomic DNA damage in telomerase-positive cells several days after drug withdrawal. This is detail of an image of HFF + hTERT cells stained by FISH-immunofluorescence using a telomere specific PNA probe (red) and γH2AX staining (green). Yellow fluorescent spots indicate co-localization of DNA damage (γH2AX) and telomere signal (TelC). ...

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Discussing recycled conference talks and developers who stop learning after 5pm (when they come home from work). Are you one of them? Can they ever be good?

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Plasmodium vivax malaria elimination can only be achieved by the deployment of 8-aminoquinolines (primaquine and tafenoquine) in combination with ACT to kill both blood and liver-stage parasites. However, primaquine and the other 8-aminoquinolines cause dose-dependent haemolysis in subjects with G6PD deficiency, an X-linked disorder of red blood cells that is very common in populations living in tropical and subtropical areas. In order to inform safer use of 8-aminoquinolines in the Greater Mekong Subregion, a multi-centre study was carried out to assess the prevalence of G6PD deficiency and to identify the main G6PD variants in samples collected in Cambodia, Lao PDR, Myanmar, Thailand and Vietnam. Blood samples were collected in the five countries during National Malaria Surveys or during Population Surveys. During Population Surveys samples were characterized for G6PD phenotype using the Fluorescent Spot Test. Samples were then genotyped for a panel of G6PD mutations. G6PD deficiency was found to be

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A myosin heavy chain polypeptide has been identified and localized in Nicotiana pollen tubes using monoclonal anti-myosin antibodies. The epitopes of these antibodies were found to reside on the myosin heavy chain head and rod portion and were, therefore, designated anti-S-1 (myosin S-1) and anti-LMM (light meromyosin). On Western blots of the total soluble pollen tube proteins, both anti-S-1 and anti-LMM label a polypeptide of approximately 175,000 Mr. Immunofluorescence microscopy shows that both antibodies yield numerous fluorescent spots throughout the whole length of the tube, often with an enrichment in the tube tip. These fluorescent spots are thought to represent vesicles and/or organelles in the pollen tubes. In addition to this common pattern, anti-S-1 stains both the generative cell and the vegetative nuclear envelope. The different staining patterns of the nucleus between anti-S-1 and anti-LMM may be caused by some organization and/or anchorage state of the myosin molecules on the ...

Cephradine (Eskacef - SKF; Velosef - Squibb) is a new semi-synthetic cephalosporin for oral use. Like other cephalosporins it is active against both Gram-negative and Gram-positive pathogens, apparently including penicillinase-producing staphylococci (though this has been questioned1). It is advertised as having new striking power, but from the data provided its spectrum of activity closely resembles that of cephalexin (Ceporex - Glaxo; Keflex - Lilly),2 and the promotional literature on cephradine makes no direct comparison between the two drugs.. ...

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BioTek Notes dapplication, 28-Feb-05, Cholesterol Quantification Using a Fluorometric Assay and Synergy HT Multi-Mode Microplate Reader

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Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. thinkBiotech performs no independent verifification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice. ...

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Product Description Product Name: MERRIC Cap 250mg 10sProduct Form: CapsulesPack Size: 10sManufactured By: MEGA PHARMACEUTICALS LTDGeneric Category: CEPHALOSPORIN ANTI-BACTERIALIngredients: Cephradine

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