細胞核試驗 的英文怎麼說
中文拼音 [xìbāohéshìyàn]
細胞核試驗
英文
nuclear tests- 細 : 形容詞1 (條狀物橫剖面小) thin; slender 2 (顆粒小) in small particles; fine 3 (音量小) thin ...
- 胞 : Ⅰ名詞1 (胞衣) afterbirth2 (同一個國家或民族的人) fellow countryman; compatriot Ⅱ形容詞(同胞...
- 核 : 核構詞成分。
- 試 : 名詞(古代占卜用的器具) astrolabe
- 驗 : 動詞1. (察看; 查考) examine; check; test 2. (產生預期的效果) prove effective; produce the expected result
- 細胞核 : nucleus; caryon; cyteblast; cell nucleus
- 細胞 : cell; sytes; bioplast; cella; [口語] gene; [生物學] cellule; cellule cellulli cellulo ; cello ; k...
- 試驗 : trial; experiment; test
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Microbiology of food and animal feeding stuffs - horizontal method for the detection and enumeration of listeria monocytogenes - part 1 : detection method - amendment 1 : modification of the isolation media, of the haemolysis test and inclusion of precision data
食品和動物飼料的微生物學.單核細胞增生性利斯特氏菌檢測和計數的水平方法.第1部分:檢測方法.修改件1 :隔離介質和溶血試驗的改進並包括精確數據Bone marrow cell micronucleus test
骨髓細胞微核試驗The protein product of meq gene was highly expressed in the nuclei of recombinant baculovirus infected sf9 cells when using an anti - meq monoclonal antibody ( mcab ) 23b46 to run the immunofluorescence assay ( fa ) ; the expression quantity and if staining patterns differed with different times post - infection ( pi ). the results of western blotting and immunoprecipitation test showed there were two specific bands around 60 kd. the results of the study demonstrated that the baculovirus / insect cell system is effective to be used to express nuclear protein of virus
結果發現:本表達系統產生的meq蛋白可被重組痘病毒表達的meq制備的單抗23b46所識別;在感染細胞中, meq蛋白僅局限於細胞核內,而且隨著感染后( pi )時間的增加,具有從核質向核仁和核膜轉移的趨向; w已stemblot和免疫沉澱試驗均證實重組桿狀病毒感染細胞裂解物中出現有兩條大小約為60kd的特異帶。This was the first successful nuclear transplant involving cells of a warm-blooded animal.
這是溫血動物細胞核移植試驗的首次成功。Mutated plasmid was transformed into e. coli tg1 cells to produce engineered peptide, then the peptide was purified by cm sepharose ion - exchange column. in vitro bactericidal assay and drug withdrawal were used to identify the bioactivity of the engineered peptide. the planar lipid bilayer membrane was used to assay the electrophysiology of the engineered peptide. toxicity studies on mammalian cells were used to assay the toxicity of the engineered peptide
將重組質粒轉化入大腸桿菌tgi工程菌中,生產構建的工程多膚,離子交換純化后獲得工程多膚初步純化產物,體外抗菌試驗、藥物撤離試驗檢測工程多膚的抗菌活性,在人工脂質膜上測定其形成離子通道的特性以初步研究抗菌機理, ?並觀察其對真核細胞的毒性作用。By fluorescence real - time pcr, we found that the expression quantity of jak2 increased along with the development of oocyte we also compared the quantity of jak2 in gv oocytes and 2 - cell embryos nuclear. the quantity of jak2 significantly reduced in 2 - cell embryo nuclear compared with gv oocytes
結果發現,隨日齡的增加, jak2的表達量也隨之增加。本試驗還比較了jak2在gv期卵母細胞和2 -細胞胚細胞核中量的變化。結果發現2 -細胞胚核中jak2的量較gv期明顯降低。We used gv and m ii oocytes to detect the exist of jak2 in nuclear via immunofluorescence. the result showed that jak2 presents abundantly in the nuclear of mouse oocyte
採取完全生長的gv期和m期的小鼠卵母細胞,以間接免疫熒光試驗檢測發現, jak2大量存在於細胞核中。Detection of mutagenicity of surface water using human lymphocyte micronucleus test
用人淋巴細胞微核試驗檢測地面水致突變性In this research, we tested 43 herbicides which include 20 different chemical classes and 11 different modes of action using 5 unicellular green algae. the results showed that chlorella pyrenoidosa was more sensitive than the other 4 algae and was suitable as target organism during herbicide screening
本研究在國內首次以5種單細胞綠藻為模式生物,參照oecd藻類生長抑制測試方法,對包括20種化學結構11種作用機制的43種商品化除草劑進行生物篩選試驗,發現蛋白核小球藻比其他4種藻更適合作為除草劑篩選中的靶標。In comparison with herbicides treating alone, the frequencies of mcn of large of experiment groups decline in varying degrees
與單獨作用相比,大部分試驗組的微核細胞率有不同程度的下降,呈現出一定的拮抗性。The activity of the antiserum was tested by dot enzyme immunization assay ( diba ) with purified antigen. western blot of hela nuclear protein extract, which contained natural hbaf53, showed that the antiserum is also a specific antiserum to natural hbaf53. therefore the highly specific and sensitive antiserum can be applied to various studies
用純化的抗原蛋白,經斑點印跡試驗測得baf53抗血清的效價,又用提取的hela細胞核蛋白(含有天然baf53蛋白)進行免疫印跡分析( westernblotting ) ,證明天然baf53蛋白也是該抗血清的抗原,說明獲得的多抗血清具有高特異性和敏感性,可用於多方面的研究。Methods ; rt - pcr method was used to amplify the coding sequence of sh2a gene. eukaryotic recombined expression vector, pcdnas. 1 - sh2a was constructed and then transfected bel7402 cell and cos
細胞激酶活性測定相關試劑二、實驗方法通過rt pcr方法擴增shzacdna編碼序列,構建真核重組表達載體pcdna3Design : viable mtb were detected in mesenteric lymph nodes, spleen and lungs at day 15, 30and 60 after intragastric administration of bcg to mice : the proliferation of t - lymphocyte with the stimulus of the purified protein derivative ( ppd ) was measured at day 60 and 90 after intragastric administration of bcg to mice ; the expression of interleukin - 2 ( il - 2 ) of t - lymphocyte in spleen was detected at day 60 and 90 after intragastric administration of bcg
方法:在小鼠胃內接種bcg的第15 , 30 , 60天,檢測結核桿菌在小鼠體內臟器的定植;接種bcg的第60 , 90天,檢測小鼠脾淋巴細胞受到ppd刺激后轉化試驗小鼠脾淋巴細胞受到ppd刺激后il - 2表達量。分享友人