肝下區 的英文怎麼說
中文拼音 [gānxiàqū]
肝下區
英文
subhepatic region-
Knowledge of distribution and regulation of ugts remains limited. liver microsomes is a frequently used enzyme source in in vitro study of glucuronidation, but it has the following deficient respects : 1. liver microsome is a mixture of various enzymes, and therefore the results from microsome cannot represent the function of a individual isozyme
關于ugts的組織分佈和調節這方面的知識還不多，過去常採用肝微粒體進行研究，但有以下缺陷： u ）肝微粒體是多種藥酶沮合的復雜體系，因而實驗結果難以區分是一種同工醇的作用6 ) according to character of zone which shen - dong diggings locates, put forward main measures of environment protection and zoology build in shen - dong diggings and surround it, full analysis water resource carrying capacity, study cleaning mining technique from reduction waste rock, fathering powder dust and deal exhaust gas pollution aspects, found environment ensuring system of sustainable development of shen - dong diggings
6 ）根據神東礦區所處地域的特點，提出了神東礦區及其周邊地區環境保護與生態建設的主要措施，對礦區水資源承載能力進行了全面分析，從減少井下出肝量、井下粉塵治理、井下廢氣污染治理等方面研究了礦山潔凈開采技術，建立了神東礦區可持續發展的環境保障體系。In order to further investigate the role of axudl in human tumor carcinogenesis and the potential association between the axudl gene expression status and the stimulation of transforming growth factor beta in human cancers, the present study was performed in three aspects as follows : ( 1 ) cloning full length enconding region cdna of axudl and construction of eukaryotic vector that expression the fusion protein of axud1 and influenza virus hemagglutin ha epitope tag ; ( 2 ) exploring the time and dose effects of tgf - 1 on the expression - of axudl gene in hepg2 hepatoma cells and spc - a1 lung carcinomas cells, and studying the effects of overexpression of axud1 on the expression of cell cycle and apoptosis related protein in hepg2 hepatoma cells ; ( 3 ) construction and expression of human axudl in e. coli m15. the following main results and conclusions can be obtained from the present study : 1. the full length ecnoding region of human axudl cdna from human peripheral blood lymphocytes was successfully cloned using one step rt - pcr method, and constructed into a eukaryotic expression vector which can be expressed a ha - axud1 fusion protein with axud1 and influenza virus hemagglutin ha epitope tag. the recombinant plasmid was identified by polymerase chain reaction, restriction endonuclease maping and sequencing, this expression vector might be instrumental to further study the function of axud1 protein in tumor cells
為了進一步研究axud1在人類腫瘤發生中的作用及axud1基因的表達狀況與tgf -介導的信號通路的關系，本實驗研究分為三個部分： （ 1 ） axud1基因cdna全長編碼區的克隆和ha表位標記的axud1基因表達載體的構建； （ 2 ）探討肝癌細胞hepg2和肺腺癌spc - a1細胞中tgf - 1誘導的axud1基因表達的時間、劑量效應以及誘導表達的可能機理，並研究axud1的過表達對細胞周期和細胞凋亡相關蛋白表達的影響； （ 3 ） axud1原核表達載體的構建及其在大腸桿菌中的表達。本實驗的主要結果和結論如下： 1利用一步法rt - pcr成功地從人類外周血淋巴細胞中克隆出axud1基因編碼區cdna ，並將其構建入真核表達載體中，編碼的ha - axud1融合蛋白帶有流感病毒凝血素ha的表位標記肽段。
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