介绍试剂盒毕业论文

酶联免疫试剂盒是基于经典酶联夹心技术原理，能测量人促卵泡素（FSH），只能用于研究用途，不得用于医学诊断。酶联免疫试剂盒工作原理促卵泡素（FSH）是动物脑垂体分泌作用于卵巢卵泡生长、发育、分化、成熟和排卵的重要繁殖激素.由于是生物大分子,不能透过细胞膜,FSH必须与靶细胞膜上的促卵泡素受体（FSHR）结合,经过受体介导将信息传递到靶细胞内,才能发挥其生物学功能.所提供的ELISA Kit是典型的夹心法酶联免疫吸附测定试剂盒（ELISA）。预先包被的抗体为多克隆抗体。检测相抗体也为多克隆抗体，经生物素（biotin）标记。样品和生物素标记抗体先后加入酶标板孔反应后，PBS或TBS洗涤。随后加入过氧化物酶标记的亲和素反应；经过PBS或TBS的彻底洗涤后用底物TMB显色。TMB在过氧化物酶的催化下转化成蓝色，并在酸的作用下转化成最终的黄色。颜色的深浅和样品中的待测因子呈正相关。酶联免疫试剂盒工作环境1． 37℃恒温箱。2． 标准规格酶标仪。3． 自动洗板机。4． 单通道或多通道可调节移液器以及其吸头。5． 蒸馏水，容量瓶等6． 干净的试管和Eppendof管酶联免疫试剂盒操作步骤1． 确定本次检测所需的已包被抗体的酶标板孔数目。2． 将倍比稀释的标准品各依次加入一排7孔中，1孔只加样品稀释液的作为对照。处理后的标本按100ul每孔加入。3． 酶标板加上盖，37℃反应90分钟。4． 反应后用自动洗板机吸去酶标板内的液体；或甩去酶标板内液体，再对着吸水纸拍几下。洗涤2次。5． 将准备好的生物素抗体工作液按每孔依次加入。37℃反应60分钟。6． TBS或 PBS洗涤3次，每次浸泡1分钟左右。7． 将准备好的ABC工作液按每孔依次加入。37℃反应30分钟。8． TBS或 PBS洗涤5次，每次浸泡1-2分钟左右。9． 按每孔依次加入TMB显色工作液，37℃避光反应，反应过程中，要经常的观察，当肉眼可见标准品的前3-4孔有 明显的梯度蓝色，后3-4孔差别不明显时，即可加入TMB终止液孔。（显色反应最长不要超过30分钟）。10． 用酶标仪在450nm测定.值。11． 根据样品的吸光值在坐标上找出对应的浓度。用户也可以使用各种应用软件来计算。应记住由于样品稀释了N倍，其实际浓度应该×N。 参考资料：

可以的，毕业论文篇幅这么大，写一点操作步骤并无不可，但不建议这样写，除非真的字数不够

With the development of knowledge economy, people's living standards have greatly improved, for health, led to the emergence of medical and health services and more strong, in vitro diagnostic reagents as an important part of medical supplies, has its enormous market potential, each production enterprises have mushroomed in all around the country, new products constantly, the domestic and international market, and the impact of this phase is associated with the lack of intellectual property. Using relevant legal economics, economics theory, is to study the legal theory and method of legal issues, it is not only related to relevant legal value has philosophical sense of legal theory, but also involves specific legal problems and almost all sectors, including intellectual property. Domestic law in introducing law of intellectual property economy class, but not involved in vitro diagnostic reagents, especially in the field of intellectual property law analysis is almost zero. This paper explains economic growth and intellectual property rights of economic relations between in vitro diagnostic reagents, intellectual property, the existing social cost and benefit the necessity and restrictive in three aspects for intellectual property protection and the use of in vitro diagnostic reagents and urgency of the problem, and reveals the in vitro diagnostic reagents fields of intellectual property law system, and puts forward the practical requirements for future improvement suggestion, the rationality of in vitro diagnostic reagents in intellectual property related legal system, and provides the reference for future : HBeAg quantitative detection in chronic hepatitis b antiviral treatment has important scientific significance and economic value, the graduation topic selection, guangzhou was antibody engineering technology Co., LTD. Is developed "hepatitis b virus e antigen (HBeAg) quantitatively kit (time-resolved immunofluorescence)", through the representative for a certain amount of research, clinical samples to assess the clinical application of test, and its effectiveness and safety to provide important basis. Methods: according to the clinical diagnostic reagents clinical research technique guiding principles for design, according to the design of clinical epidemiology, randomized controlled "three principles" and the blind, the design of the test results and diagnostic kits and re-checked results compared to assess the clinical application of kit. Results: the testing results and comparison of diagnostic kits and review kit, sensitivity achieved respectively, specificity of reco-very and , for 100% on index of and greatly, and + LR, consistent - LR less rate , kappa value and per cent for (P < ), and the correlation coefficient r = (P = ). Conclusion: the kit, accurate, reliable and stable, safe, convenient with high value of clinical applications.