1.2 Critically appraise the Clifton Gallup Strengths and Johari’s Window theories in relation to career development. 200 WORDS
1.3 Identify your key strengths for your desired career choice based on these two theories.
MY PERSONAL STRENGTHS IDENTIFIED USING GALLUP TEST : DEVELOPER, ACHIEVER, EMPATHY, IDEATION, MAXIMIZER – 200 WORDS
1.4 How you can apply elements of these theories to achieve your career aspirations?
1.4 How you can apply elements of these theories to achieve your career aspirations? 200 WORDS
MY ASPIRATION IS TO BE A MINICAB OPERATOR AGENCY – MANAGER
2.0 Know your sector Learning Outcomes
2.1 Compare and contrast two companies in your sector – what are their history, values and ethics? (choose two varied-sized companies. These could be companies you would want to work for or would be competitors) TO COMPARE: UBER – UK / VIA VAN – UK – 300 WORDS
2.2 To what extent do elements of each company’s values and ethics align with yours? – 100 WORDS
2.5 Identify and analyse a professional qualification you could acquire alongside your degree to increase your chances of being a credible professional in your sector. : MANAGER – 200 WORDS
3.0 Let them know you Learning Outcomes
3.1 How can networking help you become more commercially aware of your sector? (you should relate aspects of business news specifically to your sector: MANAGEMENT) – 300 WORDS
3.4 Reflect on what you have learnt about yourself throughout the whole module and which skills you need to further develop to be successful as an employer or an entrepreneur (give specific examples). – 200 WORDS
enzyme immunoassay (eia) or enzyme connected immunosorbant assay (elisa) is a effective method used for detecting and quantifying antigens and antibodies in medical samples. it is widely used in medical laboratories for diagnoses, prognoses and for monitoring immune responses. the purpose of this essay is to summarise the precept of this approach and to outline the main styles of enzyme linked immunosorbant assay (elisa) and its application in clinical laboratories. subsequently, it'll speak the software of this machine within the haematology field. principles the general principle of this method is based at the binding of conjugated enzyme molecule with specific antibodies to stumble on and quantify the presence of both antigens or antibodies inside the take a look at pattern. this is accompanied via adding suitable colourless substrate which catalyses the interplay complicated to provide a visible colored product. there are many chromogenic substrates used in elisa technique but the most not unusual are alkaline phosphatase (ap) and horseradish peroxidase (hrp). the quit product can be determined by the usage of spectrophotometer and the depth of shade is directly proportional to the presence of either antigens or antibodies in the test samples. sorts there are numerous sorts of elisa which consist of: oblique, sandwich, competitive, chemiluminescence and elispot assay. indirect elisa may be used to discover the antibodies which are present in patient’s serum. with this technique, affected person’s serum containing antibodies is brought to the microtitre wells which can be lined with the antigen and the depth of the cease colour product is at once proportional to the quantity of antibodies which can be present inside the patient’s pattern. (kuby) figure1. illustrate the exceptional forms of elisa to locate both antigen or antibody. the second one type of enzyme related immunosorbant assay is known as sandwich elisa, wherein the target antigen that is to be detected must be placed between antibodies. the antigen of hobby this is present within the clinical pattern is introduced to a microtitre wells that's coated with the antibody and the end product is determined by spectrophotometer to degree the amount of antigen in the scientific sample.(diagnostic micro. e-book) figure1. the development of biotechnology has grow to be full-size and one example of its progress is the amendment of elisa through the usage of chemiluminescence substrate instead of chromogenic substrate to boom the sensitivity of the reaction. with this approach, chemilumescence (cl) substrate and some improving retailers, that have the capacity to bind an antibody or antigen within the reaction, are used to create mild emissions which may be measured by particular spectrometry. this method has been used to diagnose numerous varieties of tumour sickness, and quantify numerous compounds at low attention (baeyens et al. 1998). every other example of elisa amendment is enzyme related immunospot (elispot) assay. it's far a quantitative approach often used to detect cytokines which might be secreted from unmarried cell in reaction to the antigen. throughout the incubation duration, the cytokines of hobby is launched and captured via immobilised anti-cytokines on the microtitre plate. after washing them and adding labelled anti-cytokines antibody and substrate, the quit color product presentations as a “fo>GET ANSWER