Experimental sites and Isolation of endophytic bacteria from plant tissues of maize The work was carried out in the year of 2013‚ at Embrapa Maize and Sorghum Research Center of the Embrapa (Brazilian Agricultural Research Corporation)‚ located in Sete Lagoas City (19° 27′ 57″ S; 44° 14′ 49″ W)‚ Minas Gerais State‚ Brazil. The climate is characterized by highland tropical climate (hot and warm summers)‚ and dry winters‚ savannah type‚ according to the Köppen-Geiger classification (Peel et al.‚ 2007)
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�cleaner� technologies‚ developing �greener� processes and products‚ and forming decisions related to their business activities. Green Management Accounting According to the EPA‚ green or environmental management accounting is �the identification‚ prioritization‚ quantification or qualification‚ and incorporation of environmental costs into business decisions.� Green Management Accounting uses �data about environmental costs and performance for business decisions. It collects cost‚ production‚ inventory
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According to George Ritzer‚ bureaucracy completely dehumanized the social institutions in America. He sees the bureaucracy as having four components: efficiency‚ predictability‚ control and quantification. He terms this dehumanization of an institution as "McDonaldization". One of the most prevalent examples in modern society is the health care institution. In the past‚ health care was more simplistic in nature. House calls were not unheard of‚ and doctors knew all of their patients and their families
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REVIEW OF RELATED LITERATURE The bilimbi‚ Averrhoa bilimbi‚ L.‚ (Oxalidaceae)‚ is closely alliedto the carambola but quite different in appearance‚ manner of fruiting‚flavor and uses. The only strictly English names are "cucumber tree"and "tree sorrel"‚ bestowed by the British in colonial times. "Bilimbi" isthe common name in India and has become widely used.Bilimbisare all much the same wherever they are grown‚ but P.J.Wester reported that a form with sweet fruits had been discovered inthe Philippines
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Pentacyclic Triterpene Distribution in Various Plants – Rich Sources for a New Group of Multi-Potent Plant Extracts Sebastian Jäger 1‚*‚ Holger Trojan 1‚ Thomas Kopp 1‚ Melanie N. Laszczyk 2 and Armin Scheffler 1 1 2 Carl Gustav Carus-Institute‚ Am Eichhof 30‚ D-75223 Niefern-Öschelbronn‚ Germany Betulin-Institute‚ Blumenstrasse 24‚ D-64297 Darmstadt‚ Germany; E-Mail: m.laszczyk@betulin-institut.de (M-N.L.) * Author to whom correspondence should be addressed; E-Mail: sebastian.jaeger@carus-institut
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Contents REAL TIME PCR 2 REAL-TIME QUANTITATIVE PCR (qPCR) 2 BASIC PRINCIPLE 3 TYPES OF PCR 4 qPCR STEPS 4 ONE-STEP OR TWO-STEP REACTION 6 Overview of qPCR and qRT-PCR components 6 REAL TIME PCR SYSTEM: 7 SOFTWARES FOR DATA ANALYSIS AND PRIMER DESIGNING 8 STANDARD REAL-TIME PCR PROTOCOL 9 ASSAY DESIGN 9 2. Nucleic acid purification 9 3. Reverse transcription 9 4. Controls and normalization 9 5. Standard curve evaluation of efficiency‚ sensitivity‚ and reproducibility
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Course paper: Implications of value orientation for sales practice in business markets Course title: Industrial Marketing and Purchasing in an a Business Market (FÖ2009) Made by: Yevgeniya Podolskaya 890425-T082 Lecturer: Lena Bjerhammar Date: 2012-10-09 Table of Contents Introduction 2 Purpose 3 Method 3 Literature review 3 Conceptualizing value-based selling 3 Value-based sales practice 4 Training the front-line staffs for co-creating value 7 Conclusion 8 References
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years became the most popular instrumental method of analysis. Gas chromatography is an exact imperative analytical apparatus because it can separate the chemical components in the mixture for later use or quantification. Most of the studied samples of mixtures of chemicals. If quantification method is selective for certain components in the mixture is the separation is not required. However‚ it is often the event that the detector is not explicit abundant and the first separation can be made. There
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On the frosted end of the clean grease-free slides‚ the identification number and date for each participant would be written using a glass marker. A 12µl of blood would be spread over a diameter of 15mm for thick blood film‚ while 2µl of blood would be used for a thin blood film on the same slide using an automated
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along with active back pressure regulated at 1800 psi. Calibration runs using pure lycopene standard was run at different concentrations for quantification of lycopene content in the extracted samples The identification of the peaks was carried out by comparing the retention times with those obtained with a standard solution of all-trans lycopene. The quantification was performed using the relative area under the curve. Lycopene extracted using n-hexane as a solvent at 65°C was also characterized for
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