The Bourgeoisie Essay - 1503 Words

Karl Marx describes â€Å"Society as a whole [as being] more and more [split] up into two great hostile camps, into two great classes directly facing each other-bourgeoisie and proletariat† (Marx 124). As Marx made his distinction between upper class, bourgeoisie, and lower class, proletariats, it is important to keep in mind the societal structure at the time. To understand how classes were created and the disparity between the rich and poor, or, bourgeoisie and proletariat, it is necessary to examine how people came to be rich and poor. Exploring a time before money existed will help us to process and understand reasons why the binary between rich and poor exists and how it is reflective of low and high art distinctions.†¦show more content†¦With the commodification of natural resources, there becomes a dependency between those who control the resources and all those who need to use them. At this stage of society people are no longer self-sufficient, but rely up on the network of society to provide food, shelter and jobs (Rousseau). At this level of society, the founders most often control the resources and begin to live in excess compared to the rest of the populace. Rousseau’s final stage 4) is the state of war, which is triggered when the rich deceive the poor, and the poor begin to rebel. This state of war is rooted in the transition from a free, independent mode of living to a regulated lifestyle within the constraints of society. Someone has to establish any society and as a result, those who establish society through control of the natural resources will monopolize power (Rousseau). As we see, art does not arrive until all physiological needs or the basic needs are met as is evident by the happy savage stage. Art arrives with the improvement of manual labor and hunter-gatherer techniques in the division of labor. The division of labor in turn creates divisions within society, and we can see that evidence in the French colonial enslavement of native peoples and African slave trade throughout history. The rich and poor binary canShow MoreRelatedThe Power Of The Bourgeoisie1664 Words   |  7 Pages In reaction to the power the bourgeoisie have over the proletariat, the narrator uses her defense mechanism of acting out to get power over herself back. Acting out involves preforming external actions that mirror how one is internally feeling. This can be seen when the narrator breaks a rule in the manual, and seeks affection from her window friend in the male shelter. As she states, â€Å"Tonight, his light isn’t on and so we don’t wave, but still, I undress in front of my lit window. I can’t knowRead MoreThe Communist Manifesto On The Bourgeoisie And The Proletariats1762 Words   |  8 Pageson the bourgeoisie and the proletariats. Throughout the text Marx focuses on the divide between the two classes, and the impact it had on society. Marx â€Å"the history all hitherto exi sting society is the history of class struggles.† Before the bourgeoisie rose to power, Feudal society was the dominant social system in which the upper class provided land and protection for the working class. Eventually the feudal society could not keep up with the growing demand of the market and the bourgeoisie aroseRead More Impact of the Bourgeoisie on Exploration During the Age of Discovery2315 Words   |  10 PagesImpact of the Bourgeoisie on Exploration During the Age of Discovery Thesis: Most people believe that The Age of Discovery was the product of a handful of adventurous explorers. They were an important part of this Age, but theirs was not the main motivation. I believe however, that the Bourgeoisie provided the impetus of this Age. The Bourgeoisie, a social class most distinct from the rest, remains one of the most influential economic leaders throughout Europe during the Age of DiscoveryRead MoreKarl Marx s Philosophy On The Development Of The Bourgeoisie967 Words   |  4 Pagesabout Marx’s take on the development of the bourgeoisie (the upper class), the proletariat (the lower class) and capitalism. Marx believes the bourgeoisie came out of the middle ages. He claims they were once the lower class. During the middle ages, the ruling class consisted of kings and queens, the feudal class. Following the Hegelian dialect, the normal people will get fed up of those more powerful, leading to internal contradictions. The bourgeoisie took charge of trade, as the traded the wayRead More Proletariat vs. Bourgeoisie in Karl Marxs The Communist Manifesto1065 Words   |  5 PagesProletariat vs. Bourgeoisie in Karl Marxs The Communist Manifesto In The Communist Manifesto, Karl Marx and Fredrick Engels attempt to explain the reasons for why there is class struggle and suggest how to prevent class separation. According to Marx there are two different types of social classes: the bourgeoisies and the proletarians. The bourgeoisie are capitalists who own the means of production and the proletarians are the working classes who are employed by the bourgeoisiesRead MoreThe Causes And Consequences Of Class Conflict Between The Bourgeoisie And The Proletariat1422 Words   |  6 Pagesbetween the bourgeoisie and the proletariat. The Bourgeoisie represented the members of a higher society which held onto the majority of the wealth and means also known as the owners of the means of production and the capitalists. While the proletariat class was constructed by individuals who belong to the working class or the poor. Focusing on the economic, social, and political implications of the rise of capitalism in Europe. With the r ise of capitalism, it was theorized that the bourgeoisie, a minorityRead More The Role of Autonomy and Responsibility Held by the Bourgeoisie during the Industrial Revolution1550 Words   |  7 PagesThe Role of Autonomy and Responsibility Held by the Bourgeoisie during the Industrial Revolution During the Industrial Revolution the population was broken up into two classes; the minority was the rich, industrial middle class, the bourgeoisie, and the majority was the poor working class, the proletariat. The bourgeoisie believed in their rights to gain wealth and preserve individuality and in their duty to maintain these rights, which in turn determined the harsh laboring and livingRead MoreBourgeoisie And Industrialism1154 Words   |  5 Pagesthe early years of industrialization. Both images portray a glorified view of the Bourgeoisie, who were owners of the means of production, and the Proletariat, members of the working class. These two social classes propelled the Industrial Revolution in Europe. The two images titled Orphaned Girls and Boys in a Welfare Institution, present an idealized situation of the Industrial Revolution and argue that the Bourgeoisie depended on the labor of the Proletariat for economic prosperity and survival.Read MoreThe Siege Mentality Of The Bourgeoisie1494 Words   |  6 PagesThomas G. Pelham III IB World Literature Dr. Smith 20 May 2015 The Siege Mentality of the Bourgeoisie in Ibsen’s A Doll House By the time of Ibsen’s A Doll House (1879) the bourgeoisie was firmly established as the dominant class in Europe. To legitimize their power capitalists defined themselves against other classes, claiming they possessed inherent qualities justifying their position. A rigid moral system and social code reinforced class stratification. These structures also enforced conformityRead MoreMarx and the Bourgeoisie Essay1908 Words   |  8 Pagesessay I plan to analyze the claim by Karl Marx that the bourgeoisie class produces its own gravediggers. I will first present a definition of the bourgeoisie and the proletariat classes along with what Marx means by his claim. After discussing Marxs claim and his support I will assert that his claim is false and was based on a false assumption. I will argue that Marx does not allow the possibility of an adaptation on behalf of the bourgeoisie. Furthermore, that Marx contradicts his claim with his

Capital Mobility And The Financial Crisis - 1918 Words

Capital mobility in the Eurozone ECO209 paper assignment Lei Lin #1000672195 Introduction: As the economy becomes more and more integrated, the trade barriers between individual countries are gradually removed. People now have more options in terms of goods, services, and of course investments, meaning capital flows are more mobile nowadays. However, deregulation of the capital raises controversy and concerns about whether if increasing capital mobility is going to bring prosperity, not only to the world economy in general, but to each country individually. According to Helleiner (1994), high capital mobility is claimed to be one of the causes to the 09 financial crisis as huge capital inflow entered into the US border and changed the housing structure and then gave rise to the easy mortgage credit and housing bubbles. However, this paper intends to find the link between the capital mobility and the financial crisis in order to see if this tragic outcome is inevitable when we have a relatively high capital mobility. The paper takes the stance that increase capital mobility is going to ultimately benefit the world economy as well as bring opportunities to countries that are ready to liberate their capital flow. The article is taking the case study approach and focuses on Europe Union before, during and after the financial crisis, as EU seems to be promising to have some convincing empirical evidence. The purpose of the paper is to show advantages of having a highShow MoreRelatedBenefits Of Developing Countries Adopting Capital Controls During A Recession1529 Words   |  7 PagesCapital control is defined as a type of measure governments can use to regulate and restrict the amount of money flowing from capital markets in order to keep inflation under control while maintaining a competitive real exchange rate. International Monetary Fund (IMF) has been slowly shifting its beliefs to where capital control policies can be deemed useful for countries during a potential crisis. Some countries, especially the developing ones that implemented capital contro l policies have experiencedRead MoreArticle Analysis: On the Contradictions of the New International Financial Architecture: Another Procrustean Bed for Emerging Markets?1404 Words   |  6 PagesSummary: what is a main concept in the case or article? The main concept of the article is to explain why the New International Financial Architecture (NIFA) was created and who is being benefited from this approach. The discussion begins with an examination of the power structures of the global political economy by focusing on the continued dominance of the USA. The article presents the contradictory relations between USA and global finance will be explored so as to shed more critical lightRead Moreâ€Å"the Rapid Expansion of International Financial Market Since Early 1980s Have Integrated the World Economy†. Discuss.1243 Words   |  5 Pagesâ€Å"The rapid expansion of international financial market since early 1980s have integrated the world economy†. Discuss. The international financial system is a structure of markets within which organizations and individuals trade to support economic commitments made across national borders where buyers and sellers participate in the trade of assets such as equities, bonds, currencies and derivatives. 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Group Manuscript Free Essays

Bacterial cells are a common choice for in vivo replication of DNA of interest, and in this study, the heat shock method was employed for bacterial transformation. Plasmids, which are DNA molecules themselves, were used as expression vectors for the DNA of interest, the GAP gene. Because only transformed cells exhibit antibiotic resistance, trans armed cells survived on plates containing inclining. We will write a custom essay sample on Group Manuscript or any similar topic only for you Order Now Only those cells that took up plasmid s containing the GAP gene fluoresced in IV light. By restriction enzyme analysis and gel electro prophesiers, the relationship between genotype and phenotype was observed using isolated p zamias from the bacteria. Because the presence of the GAP gene codes for fluorescence, it is expected t hat a genotype coding for the protein would express the glowing phenotype. Regular action of GAP gene expression was observed in samples that were grown with rabbinate, inimical in, and varying amounts Of glucose. Our results Suggest that the presence Of glucose in the s rounding environment inhibited transcription from the rabbinate bad promoter. Age 3 INTRODUCTION This study examined the transcriptional regulation Of the rabbinate Oberon pr emoted found in Escherichia coli (E. Coli). To facilitate this study, the Green Fluorescence t protein (GAP) was utilized as a reporter gene with the rabbinate promoter. The KEEP gene w as 772 base pairs (BP) long and was extracted from Quarrel Victoria. This gene was implanted into plasmids, which were inse rted into the E. Coli through bacterial transformation (3). In order to obtain enough copies of these DNA samples in a reasonable ammo NT of time, two methods can be used. The first is considered in vitro , or in glass, (such as a test tube) and is known as polymerase chain reaction. This method, in which a machine heats t he DNA sample ND Tag polymerase clones the DNA, is expensive and less convenient, so it is not always used. The other method is In Vivo , or in life, and is called transformation. This method was used in this experiment by shocking E. Coli bacteria with heat in order for them to take in plasmids that were transformed to contain the GAP gene. Not all bacteria were transformed, and not all transformed bacteria contained the GAP gene. To differentiate between transformed and n untransformed bacteria, they were grown on inclining, as the transformed bacteria were rest assistant to impact Olin but the untransformed bacteria were killed by it. The plasmids with and with out the GAP gene were differentiated by visualization under IV light (4). The genotype of the remaining plasmids, both transformed and nontransparent med, were then tested to determine the relationship between the genotype, or plasmid c imposition, and phenotype, or presence of fluorescence. The plasmids were removed from the e bacteria, with some samples left whole as controls and others cut into pieces by restriction enzymes. In this case, doll, originating from Hemophilia influenza , was the enzyme used to cut the plasmids Page 4 at their respective Hind doll sites, where the GAP gene would have been inserted. This was done to determine whether or not the KEEP gene was taken in by the plasmids when it was electrophoresis, as the difference in size of the pieces was observed in the gag arose gel (4). Even though a transformed bacterium may have had the GAP gene in its insert Ted plasmid, it needed the promoter bad (consisting of genes Arab, area, and award) and t he GAP gene in the right direction and position in order for the bacterium to have the potent al for fluorescence. It may still not have fluoresced if there was not enough rabbinate present for the bad promoter to run, or if a high concentration of glucose inside the cell was present to rep as the bad promoter. With all the necessary genetic coding for fluorescence, the amount that was visible depended on the amount of glucose present, as no glucose caused it to floorer see brightly, and a low concentration made it glow dully (4). Each step of this experiment was vital in analyzing the transcriptional regulate on of the rabbinate Oberon promoter. Through bacterial transformation, recombinant DNA and cloning methods were used in order to insert the GAP gene into the plasmid. The pellet of cells was then resume need using a pipette and vortex mixer. This allows for a XX concentration to be obtained. After spreading, the four plates were incubated upside down (overnight at 370 C) in a microbial incubator. Following incubation each plate was placed upside down n a IV box and photographed. Restriction Analysis In restriction analysis, two restriction enzyme digestion reactions (one uncut b Y enzyme, one cut by enzyme) occurred for each of the two DNA samples (nonresistant and non page 6 fluorescent, resistant and inflorescent, and resistant and fluorescent). For the uncut samples, components were added in the following order: Pl XIX Buffer ( supplied by environment by life technologies†Ã¢â‚¬Ëœ containing: 100 mm Trisect, pH 7. 5 100 mm Magical mm Theoretical 500 mm Nasal), 1 Pl Water, and 5 Pl DNA For the uncut samples, components were e added in the allowing order: Pl XIX Buffer, Pl Water, pi DNA, and III Handbill NZ. (sup plied by invitation by life technologies†Ã¢â‚¬ ). After all components were added they were mixed by overexerting and collected at the bottom of the tubes by using the microelectronic gem The tubes were then incubated for 30 minutes at 37 co. Following incubation, Pl of XIX loading g buffer (1% (w/v) SD (sodium decoded sulfate) 50% (v/v) glycerol 0. 05% (w/ v) bronchiole blue) was added to each tube. The samples were mixed by overexerting and collected at the e bottom of the tubes using the microelectronic- Agrees gel electrophoresis was prepared by ding Pl of 1 KGB plus ladder ( supplied by environment by life technologies†Ã¢â‚¬ ) into the first and final well. 12. Pl of each sample was then loaded into remaining wells on the gel and the electro prioress was run for 1 hour at 1 VIVO. The gels were then placed in a IV box and photographed. Using the photo of the gel, the genotypes of each sample were verified. This was done by finding the size of fragments through comparison with the DNA standard ladder. Gene Expression TO allow for observation Of phenotypes gene expression, bacteria were transfer erred to three types of media: inducing, introducing, and repressing. Five plates were used: LB,’Amp, LB/Marry, LB/Amp/AR/Glue 0. 2%, LB/Amp/AR/Glue 0. 5%, LB/ Amp/AR/Glue 2% (xx). On each plate, bacteria with empty plasmids and therefore no GAP gene for flour essence were spread on one half, and bacteria with plasmids containing the GAP insert were e transferred to the Page 7 other. Both of these types of cells came from a master plate. Using a sterile to toothpick, each type of bacteria was patched in the appropriate area of each plate. GAP+ bacteria were patched in a â€Å"+† shape, while GAP bacteria were patched in a shape. Plates were labeled properly and Leary and were placed Poseidon in a ICC incubator overnight. Plates were e observed for fluorescent bacteria on the IV transformational box after 24 hours, after 72 h ours, and again after 96 hours. Page 8 RESULTS Bacterial Transformation In order to investigate GAP gene expression, it was first necessary to obtain co pies of the DNA of interest through bacterial transformation, which allowed for plasmid ( and sometimes GAP) uptake by numerous bacterium. Phenotypes results from this procedure can suggest possible genotypes. Transformation plates that were prepared after heat shoo KC transformation can be Seen in Figure 2. Individual colonies were visible on each AMP+ plate, while a lawn of bacteria had formed on the AMP plate and individual colonies were not discern enable. Under IV light, fluorescence was observed in those colonies expressing the GAP gene. If guru E highlights the difference observed between glowing and knowing bacterial colonies. The fraction of colonies that appear fluorescent and are assumed to be GAP+ is noted in Table e 1 along with complete results of this bacterial transformation (4). Structural Analysis by Restriction Analysis and Gel Electrophoresis TO confirm the structure Of DNA plasmid genotypes, samples were run through h gel electrophoresis after being treated with a restriction enzyme specific for cleave ins the gene of interest (GAP). Standards were run along with each of the components on the electrophoresis gel. In order to determine size in base pairs of fragments of interest, a graph of the e relationship between the size and migration of the bands in the 1 KGB plus DNA Ladder was assembled (Figure 4), and a line of best fit was determined. The relationship between the base 1 O log of size and migration is linear, and graphing them together gave a trend line with an ex. action useful in determining the size of experimental fragments with known migration values. These were the fragments obtained by cleaving the plasmids with the Handbill restriction enzyme. Table 2 page 9 organizes the sizes and migration distances for the fragments of the standard included during electrophoresis. These values were used to construct the calibration curve m mentioned before (Figure 4). Figure 3 shows the agrees gel obtained by gel electrophoresis. Ta able 3 lists all sizes determined based on comparison with the calibration curve generated from migration standards (Figure 4). Sizes are noted for both the vector and the insert (4). Analysis of Reporter Gene Expression Investigation of gene regulation and interaction of environmental rabbinate a ND/or glucose with genotype required GAP+ cells to be spread on various plates, an d fluorescence to be observed over time. Table 4 summarizes the observations of the phenotype o f patches streaked onto AMP plates containing or lacking rabbinate and/ or glucose. Glowing patches suggest expression of the GAP gene. Observations show that the rabbinate sample pop site for the GAP insert fluoresced brightly as time went on. The sample with rabbinate and 0. 2 % glucose increasingly fluoresced over time, while plates higher in percentage glucose c imposition did not fluoresce. Cells that were GAP were also spread in order to serve as a surrogate et marker. These cells do not contain the gene for GAP, so they will not fluoresce under IV light . This gives a comparison, making it easier to determine if cells are expressing GAP fluoresce once or not page 10 DISCUSSION Regulation of Gene Expression: The samples that were grown with rabbinate, inclining, and varying amounts of glucose showed that the presence of glucose in a bacterium’s surrounding environment NT can affect the ability of its rabbinate bad promoter. The plate with no glucose added flour cede brightly, while the plates with glucose added showed very little to no fluorescence. The only plate with glucose added that fluoresced in the end was the plate with the least glucose added These results are due to the glucose inhibiting the rabbinate Oberon from trap inscribing the bad promoter DNA. When glucose is present in a bacterium, the cell metal likes the glucose instead of the rabbinate, and the rabbinate Oberon is not utilized. However, when the cell is lacking glucose, it reaches a state of â€Å"hunger† and begins producing cyclic adenosine Mephistopheles (CAMP). This reacts with the CAMP receptor protein (CROP), who chi allows the cell to use rabbinate to induce the transcription of the rabbinate bad prom otter. This promoter contains the genes Arab area , and award, which are part of the rabbinate Oberon. This system can only function if rabbinate is present in the cell; otherwise the gene arc will prevent the rabbinate Oberon from carrying out transcription by forming a â€Å"knot,† or loop in the DNA The rabbinate bad promoter reacts with the GAP gene to show when the Arabian SSE Oberon is in use and how strongly it is induced by rabbinate (5). The plate with the least glucose added began to glow over time, as the cell be an using up the glucose in its environment by metabolize it for energy. It started to FL recurrences dully once the concentration of glucose was not high enough to fully repress the AR baboons Oberon, showing that there is a range of repression and induction, not just a state of † on† and â€Å"off’ for page 11 these function. The more the bacteria used the glucose, the less of it was arrow ND to repress the Oberon, which is why its fluorescence strength grew over time. If the study WA s to be continued past the 96 hour mark, all of the plates would have eventually fluoresced as t hey used up their loses resources and began activating the rabbinate Oberon (4). How to cite Group Manuscript, Papers