特異性因子 的英文怎麼說
中文拼音 [tèyìxìngyīnzi]
特異性因子
英文
specific factor- 特 : Ⅰ形容詞(特殊; 超出一般) particular; special; exceptional; unusual Ⅱ副詞1 (特別) especially; v...
- 異 : 形容詞1 (有分別; 不相同) different 2 (奇異; 特別) strange; unusual; extraordinary 3 (另外的;...
- 性 : Ⅰ名詞1 (性格) nature; character; disposition 2 (性能; 性質) property; quality 3 (性別) sex ...
- 因 : Ⅰ動詞[書面語] (沿襲) follow; carry on Ⅱ介詞1 [書面語] (憑借; 根據) on the basis of; in accord...
- 子 : 子Ⅰ名詞1 (兒子) son 2 (人的通稱) person 3 (古代特指有學問的男人) ancient title of respect f...
- 特異性 : distinction
- 特異 : 1 (特別優異) exceptionally good; excellent; superfine2 (特殊) peculiar; distinctive特異功能 s...
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Newcastle disease virus ( ndv ) strain 695, a thermostable nature avirulent strain, were replicated in embryonated chicken eggsand its rna was extracted from allantoic fluid. referred to the reported sequence of f gene, a pair of primers were designed and synthesized. f gene of ndv b95 strain was amplified by rt - pcr, the pcr products were checked by agrose gel electrophoresis and purified by agrose gel fracion method
利用從國外引進的新城疫熱穩定性天然弱毒b _ ( 95 )株接種spf雞胚繁殖病毒,經處理后提取病毒的基因組rna ,參考國內外發表的ndv融合蛋白基因序列,設計一對特異性引物,經反轉錄聚合酶鏈式反應( rt - pcr )擴增出約1700bp大小的特異性片段,將此片段回收純化后,利用t - a克隆技術將其克隆到pgem - t - easy克隆載體中,再轉化大腸桿菌jm109感受態細胞,轉化后經分子量比較、 pcr鑒定和酶切分析篩選陽性克隆。It was suggested that eric - pcr could substitute for rapd in research related to the genetic identification and genetic diversity in auricularia and other edible and medicinal fungi : 2 to a certain extent, genetic differences among auricularia strains tested in this study did not have necessary relativity with their geographical origins respectively ; 3 in this study, genetic diversity in a. polytricha was higher than that in a. auricula : 4 in this study, a. fuscosuccinea had a higher homology to a. auricula than to a. polytricha ; 5 morphological characteristics validated the results from eric - pcr and provided a potential explanation for the higher similarity coefficient between a. auricular and a. fuscosuccinea ; 6 southern hybridization was employed by choosing a strain from a. auricula as a probe which hybridized with a. auricula and a. fuscosuccinea except a. polytricha, further confirming the veracity of the results from eric - pcr ; 7 in this study, isozyme analysis could not cluster the 7 strains from three auricularia species to different groups efficiently ; 8 2 strains from two auricularia species revealed high conservative degree and the restriction fragment patterns by 4 kinds of restricted enzymes showed no diversity
本研究中,木耳屬2個種的2個菌株在its區域表現出較高的保守性, 4種限制型內切酶的酶切圖譜沒有顯示出多態性;增加內切酶種類及供試菌株數量,有可能獲得具有多態性的限制性內切酶酶切圖譜; 9本實驗中, its區域的真菌特異性引物與真核生物通用引物對于擴增效果無較大差異,擴增片段長度均為650bp左右; 10根據形態學實驗、 eric - pcr實驗以及southern雜交實驗的結果分析,紫木木耳屬種質資源的遺傳鑒定和遺傳多樣性評價耳極有可能是毛木耳種的一個變種; n .本研究中所用的gutc法是一種適用於木耳屬菌株基因組洲a快速提取的方法; 12 .傳統的形態學分類法和現代的分子生物學分類法,兩者的關系是相輔相成,互為驗證Human augmenter of liver regeneration ( halr ) is a novel cytokine which stimulates specifically hepatic cell proliferation and is able to rescue acute liver failure caused by hepatotoxin for example carbon tetrachloride and galactosan amine et al
人肝再生增強因子( humanaugmenterofliverregeneration , halr )是一種新的細胞因子,能特異性地刺激肝源細胞的增殖,並對四氯化碳、半乳糖胺等肝毒劑引起的肝損傷有治療作用。While the suppression of ( - arrestin2 endogenous expression by antisense or rnai technology considerably attenuated sdf - 1 ( - induced cell migration. expression of ( - arrestin2 also augmented chemokine receptor ccr5 - mediated but not egf receptor - mediated chemotaxis, indicating the specific effect of ( - arrestin2
與此相似,另一種趨化因子受體ccr5介導的趨化作用也受- arrestin2的調控,但egf受體介導的趨化作用則不受- arrestin2的調控,說明- arrestin2的作用有一定的受體特異性。These results show that coda gene cloned from e. coli can express specifically in the anther of both monocotyledon and dicotyledon plant species upon induction of 5 - fc, and the in vivo expression product of the gene can transform the 5 - fc used externally into 5 - fu, which leads to all or partial inactivity of anthers and / or pollens
以上結果表明, coda基因在單子葉植物和雙子葉植物花藥中的特異性表達,能將外用的5 - fc在體內轉化為5 - fu ,導致花藥或花粉的部分和全部失活。These results suggested that dgp1 could drive target gene expressed mainly in guard cells when plant is subjected to drought stress
這些結果證明,在植物遭遇乾旱脅迫時, dgp1啟動子可以驅動目的基因在保衛細胞中特異性表達。Molecular basis of neural - specific gene expression
神經特異性基因表達的分子基礎In this paper, a field strain of infectious bronchitis virus was isolated from proventriculus tissue, morphological observation by electron - microscope and the biological characterizations of the virus were studied, pairs of specific primers are designed and synthesized in correspondence with them, according to the published sequences of infectious bronchitis virus three structural protein ( spike protein s membrane protein m nucleocapsid protein n ) genes, the cdna of si gene, s2 gene, m gene. n gene of ib v isolate lx4 were amplified by rt - pcr and full sequences were first reported
在此基礎上,根據國內外已發表的ibv基因序列,分別設計特異性引物,應用不同引物進行反轉錄合成cdna ,分片段對ibv的主要結構基因進行pcr擴增,並分別將各個目的片段克隆到puc19載體上,在大腸桿菌dh5中實現目的基因的分子克隆,經藍白斑篩選、限制性內切酶分析、 pcr鑒定,篩選出重組陽性質粒,並對各個目的基因片段進行序列測定,從而獲得ibv主要結構基因全序列。7. at the first time, the reporter dye, fam was linked to the 5 " - end of the oligonucleotides of the probes, and the tamra was located at the 3 " - end as quencher dye. we use camv35s and fmv promoter, nos terminater, mark gene nptii, and aim gene pat, epsps and cryla ( b ) genes as target sequences, design pairs of sp
7 、首次以fam熒光素標記探針5 』端作為發光基團,以tarma標記探針3 』端為淬滅基團,以camv35s 、 fmv啟動子、 nos終止子、標記基因nptll 、抗除草劑基因epsps 、 pat 、抗蟲基因cry1a )為檢狽目標,設計、篩選出特異性引物和探針,優化實驗參數,建立了轉基因植物通用性熒光pcr定性檢測方法體系。Deduced amino acid sequence of s1, s2, pvin were also highly homologous each other ( 98 %, 99 % in each case ). the stilbene synthase genes were excised from the plasmids by bamh i and sac i digestion and intergrated into a binary vector, pbi121 and pev2, from which the p - glucuronidase ( gus ) gene sequence had been removed by the same digestion to prepare a 35s promoter - stilbene synthase 2 - nopaline synthase polyadenylation site construct and a tfp2 promoter - stilbene synthase 1 - nopaline synthase polyadenylation site construct. the recombinant plasmids were called pbs2, pev2s 1. respectively
用bamhi和saci同時酶切ps2 ( s2表示來自雷司令的芪合酶基因) 、 ps1 ( s1表示來自粉紅玫瑰的芪合酶基因)以及pbi121 、 pev2 ,使得s2 、 s1分別插入替代pbi121 、 pev2中的gus基因,構建成植物表達載體pbs2 、 pev2s1 , pbs2中含camv35s組成型啟動子,使s2基因能在番茄植株的各個部位表達; pev2s1則含有果實特異性啟動子tfp2 ,使s1基因只在番茄果實中表達。Advances on tissue specific promoter in suicide gene therapy of prostate cancer
前列腺癌自殺基因治療中組織特異性啟動子的研究進展Multiplicity of signals and diversity of signaling pathways exist during the establishment of mycorrhizal associations together with the regulation of symbiosis - specific genes expression. this mechanism of signal recognition and transduction related with development process of the symbiont was reviewed at the molecular level
在菌根共生體建立過程中存在信號分子的多重性和信號通路的多樣性以及共牛體特異基因的表達調控,從分子水平上揭示了菌根整個發育過程。The loop sequence of mb1 and mb2 were the anti sense and sense sequence ofing1, respectively the sequence of mb3 was a piece of ssrna sequence in tobacco mosaic virus, which had no analogical to human gene. mbl was the most suitable probe because mbl had the highest fluorescence enhancemen after hybridizing wtth rna extrated froin normal cell
第三章,根據一種常見的病毒煙草花葉病毒( tmv )的核酸序列設計了分子信標熒光探針,由於tmv的遺傳物質是rna ,分子信標又具有很高的特異性和靈敏度,因此感染了病毒粒子的植物葉片在經過簡單處理后,可用分子信標檢測葉片上。Preparation and identification of - fetoprotein specific transfer factor
甲胎蛋白特異性轉移因子的制備和鑒定Preparation and identification of specific transfer factor for hepatitis b virus
乙型肝炎特異性轉移因子的制備及鑒定It still remains a question whether the rearrangements of igh come from h / rs cell or the background lymphocytes. in this study, we have detected the igh clonal correlation between the h / rs cells and the background cells, from a new aspect to study the clonality of h / rs cell and its relation with the background cells. the expression of b - cell - specific activator protein ( bsap ) was detected in hl. igh gene rearrangements were analysed by the methods including gene analysis in neoplasms tissue and micropicked cells from paraffin - embedded sections, sequencing to test the pcr product, and in situ pcr
本研究將在以往研究的基礎上,在國內率先把b細胞核反式作用因子? b細胞特異性激活蛋白( b - cell - specificactivatorprotein , bsap )應用於hl的研究,檢測hl的bsap表達,並採用石蠟刮片組織和微切割單細胞的基因分析、測序分析和間接原位pcr等方法,同步觀察分析h rs和背景淋巴細胞的igh基因克隆相關性,從又一個新視角探究chl的腫瘤性h rs細胞克隆性及與背景淋巴細胞的關系。1. a new method to identify _ amylase activity and its producing bacteria : the blue complex was formed by unspecific adsorption, after mixing starch and trypan _ blue. the adsorption weakened when the starch was hydrolyzed to small molecular by _ amylase, and the trypan _ blue was released inside the hydrolyed zone. the starch around the zone which was not hydrolyzed adsorbed free trypan - blue so that the colour of medium became bluer than that of place in hydrolyzed zone
快速鑒定並篩選-澱粉酶及其產生菌的新方法:錐蟲藍染料和澱粉由於靜電非特異性吸附結合后使澱粉呈穩定的藍色,當澱粉被澱粉酶水解后因分子變小吸附力減弱,而讓錐蟲藍游離出來,游離的錐蟲藍被周圍未水解的澱粉吸附而使顏色加深,澱粉水解區則形成無色、透明的水解圈。As a member of an important transcription factor family, ap - 2 a expresses in specific tissue and binds with specific dna sequence
Ap - 2作為一個重要的轉錄因子ap - 2家族的成員,具有組織表達特異性和dna結合特異性。The research effort focused on the structure, function, gene engineering and expression of specific sperm membrane protein. he has been actively engaged in this field for over 30 years, and published more than 70 research papers in international and national journals
年他建立了雄性生殖細胞生物學組,近十余年來主要從事特異性精子膜蛋白的結構,功能及基因工程和表達的研究。The transgenic goldfish were detected and screened by pcr, southern blot. the results showed that pcr amplify a 478bp specific molecular band in 5 individuals, southern blot results showed a strong signal in transgenic fish
Pcr檢測結果顯示,有5尾轉化個體的總dna能擴增出一條478bp的特異性分子帶,說明轉化個體整合有gfp基因,整合率為42 。分享友人