INDEX (1) SOYBEAN- THE SOURCE OF SOYMILK 2 (2) ORGIN 3 (3) SOY MILK 4 (4) PREPARATION OF SOY MILK 6 (5) COMPARISON BETWEEN SOYMILK& NATURAL MILK 8 (6) ADVANTAGES & DISADVANTAGES 12 (7)
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There are two major steps that affect the sensitivity and specificity of AQD-Tn mAb probe: blocking time and staining time. First‚ blocking time was investigated. Different time periods were examined and it was narrowed down to 15minutes as the sufficient blocking time. Smaller time intervals were studied to further shorten the blocking time. As shown in Figure
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were then co-incubated with different nanoparticles for 4h. After removing the culture medium‚ the cells were incubated with a diluted DCFH-DA reactive oxygen species (ROS) probe for 20 minutes and observed under a microscope after washing away the staining solution. Evaluation of in vitro therapeutic effect of human tracheal epithelial cells‚ HTEpiC‚ were procured from the Cell Bank of the Chinese Academy of Sciences in Shanghai. These cells were grown in a specialized culture medium and exposed to
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Observation of mitosis in garlic root tips Abstract The purpose of this experiment was to establish the different stages of mitosis which occur in the tip of a garlic root. The root tip which was used had already been pre-stained with an aceto-orecein stain. The stain made the root tips more visible so that under a light microscope it would be much easier to distinguish where the root tip was. While under the light microscope the objective was to be able to identify and distinguish each of the stages
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bioreactive has been producing the more favorable results‚ and as in this figure bioreactive shows better results as expected. 8a. Summarize the results from figure 4 in your own words. During the 14-day measurement the MCS’s cells show more staining for Annexin V in the static lungs than the bioreactive as well increased PCNA for the bioreactive lungs. C10 contained higher levels of Annexin V during the 11-day measurement for static lungs‚ less were present in the bioreactive lungs. 8b.
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CHAPTER I INTRODUCTION Pneumonia is one of the most common infectious diseases prevalent nowadays and affects all ages. It is an acute or chronic infection of one or both lungs caused by microorganisms‚ such as viruses‚ bacteria or chemical irritants. (Schmitt‚ 2011) It has different types‚ and one of them is Community Acquired Pneumonia (CAP). CAP is a disease in which individuals who have not recently been hospitalized develop an infection of the lungs. It occurs because the areas of the lung
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I. Sampling : a procedure for obtaining a random sample Goal Estimate characteristics of a fabric by testing a few pieces(specimens) Estimate is more ACCURATE if specimens chosen RANDOMLY ** Randomization : each element has the same probability of selection as does every other element HOW accomplish random sampling? 1. Obtain a sample SAMPLING FLOW CHART A. Production lot One manufacturer’s production made from the same raw material under the same condition ( the population) Source of
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‘slice extremely thin sections for viewing under the microscopes’ as Robert Hooke found that cutting a cork in a thin section gets a clearer view. As technological advances advanced new techniques also developed over time for example staining techniques. Staining techniques was developed to view and understand tissues under the microscope by using dyes to stain tissue and visualise
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Microorganisms are classified according to their structure. By means of flow charts‚ diagrams and tables explain the differences between Viruses‚ Bacteria‚ Cyanobacteria‚ Achaea and Fungi. Bacteria or bacterium are unicellular microorganisms. They are essentially only a few micrometres long and form of various shapes including the spheres‚ rods and spirals. A BACTERIAL CELL Illustration courtesy of Wikipedia. A Virus (from the Latin noun virus‚ meaning toxic or poison) is a sub-microscopic
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1. The final yield of the cells can be determined by use of an automated cell counter or by use of a hemocytometer (Neubauer chamber). In our laboratory‚ we determine the number of purified cells in a Neubauer-improved‚ bright line chamber with V-slash with a depth of 0.1 mm and a counting area of 0.0025 mm2 from Marienfeld (Lauda Königshofen‚ Germany‚ PN # 0650030). 2. For determination of the final cell yield‚ mix a 10 µl aliquot of the purified cells (Figure 9D) with 10 µl of trypan blue solution
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