染色質核蛋白 的英文怎麼說

中文拼音 [rǎnshǎizhídànbái]
染色質核蛋白 英文
chromonucleoprotein
  • : Ⅰ動詞1 (用染料著色)dye 2 (感染) catch [contract] (a disease) 3 (沾染) acquire (a bad hab...
  • : 色名詞[口語] (顏色) colour
  • : Ⅰ名詞1 (性質; 本質) nature; character; essence 2 (質量) quality 3 (物質) matter; substance;...
  • : 核構詞成分。
  • : 名詞1. (鳥類或龜、蛇類所產的卵) egg 2. (像蛋形的東西) an egg-shaped thing 3. (辱罵之詞)
  • : Ⅰ形容詞1 (似雪的顏色) white 2 (清楚; 明白; 弄明白) clear 3 (空的; 沒加他物的) pure; clear; ...
  • 染色 : dye; dyeing; colouration; tintage; tinging; dyschroia; colouring; colour; [半] decoration染色不足...
  • 蛋白 : 1. (卵中透明的膠狀物質) egg white; albumen; gary2. [生物化學] (蛋白質) protein
  1. In eukaryotic cells, dna is located in nucleolus in the form of chromatin by combining with histone proteins

    在真生物中, dna分子纏繞在組上形成保存在細胞的細胞中。
  2. Methods : hyperosmotic pressure animal model was established by administering 3 % sodium chloride as drinking water to rats or increasing osmotic pressure of the culture medium. osmoregulation positions in the brain, reciprocal projection pathways between the medullary visceral zone ( mvz ) and supraoptic nucleus ( son ) or hypothalamic paraventricular nucleus ( pvn ), oscillation of intracellular calcium in cultured neurons and astrocytes were studied by means of anti - fos, glial fibrillary acidic protein ( gfap ), tyrosine hydroxylase ( th ) or vasopressin ( vp ) multiple imrnunohistochemical staining, immuno - electronic microscope, wga - hrp retrogradely tracing and cell culture methods. results : ( 1 ) fos positive neurons within the mvz, parabrachial nuclei, locus ceruleus, pvn, son, subfomical organ increased markedly

    方法:通過給予大鼠飲用3氯化鈉或提高培養基滲透壓濃度的方法復制高滲刺激模型,主要採用抗fos 、膠原纖維酸性( gfap )和酪氨酸羥化酶( th ) (或加壓素? vp )免疫組織化學多重、免疫電鏡、 wga - hrp束路追蹤結合免疫組織化學多重、細胞培養等實驗方法,系統觀察了中樞參與滲透壓反射的調控部位、下丘腦視上( son )神經元? ast超微結構的變化、延髓內臟帶( mvz )和son及下丘腦室旁( pvn )之間往返投射通路和神經元的性及其與ast的關系、培養神經元和ast內鈣波的變化。
  3. After the recombinant plasmid pcdna3. 1 / ts87 was identified by digestion of hindlll and bamh i, it transformed into cos7 by lipofectamine. expression product was identified by immunohistochemical method, sds - page and western - blot. the immunocytochemistry result has shown that specific brown - staining grains were found in the cytoplasm of cells transformed by recombinant plasmid versus not seen in cells transformed by pcdna3. 1 or normal cells ; the sds - page result has revealed that a band about 3 8kb was found in cell lysis transformed by recombinant plasmid versus not in cells transformed by pcdnas. l or normal cells ; the western - blot result has showed that only the band about 38kd was recognized by sera from rabbit infected by t. s artificially and sera from rabbit immunized with soluble antigen of t. s and with protein expressed by ts87 gene and by a monoclonal antibody of t. s

    通過細胞的免疫組化,細胞裂解物的sds - page電泳, westem - blot分析檢測目的基因的表達情況。免疫組化結果顯示:重組粒轉的細胞中有棕褐顆粒,而空載體轉細胞及正常細胞無此現象;細胞裂解物sds - page電泳結果顯示:只有重組粒轉的細胞在約38kd處有明顯的帶,這與理論計算的ts87基因表達的分子量為38kd基本一致; western - blot分析結果顯示:約38kd的帶能夠分別被旋毛蟲感兔血清,成蟲蟲體可溶性抗原免疫兔血清, ts87基因原表達免疫兔血清( ts87血清)以及一株具保護性的旋毛蟲單抗特異識別。
  4. Epigenetic modification of the genome ensures proper gene activation during development and involves : genome methylation changes ; the assembly of histon and histone variants into nucleosomes and remodeling of other chromatin - associated proteins such as linker histones, polycomb group, nuclear scaffold protein, and transcription factors

    這些的再程序化包括dna的甲基化和小體組的乙酰化等。組乙酰化在結構調節、 dna復制、基因轉錄、細胞分化及癌細胞發育都有研究,但在克隆動物中卻是一個有待深入探索的領域。
  5. Telomerase is a ribonucleoprotein complex ( rnp ) composed by its rna component and protein subunits. telomerase can synthesize telomeric dna onto chromosomal ends using its own rna component as a template, elongate the length of telomere, increase cell life and even induce cell immortalization

    端粒酶( telomerase )是由端粒酶rna和組成的一種復合物( rnp ) 。端粒酶含有引物特異識別位點,能以自身rna為模板,逆轉錄合成端粒dna並加到體末端,使端粒延長,從而延長細胞的壽命甚至使其永生化。
  6. In this paper, the effect of nuclear actin on the process of chromosome construction has been studied by utilizing the precise natural synchrous plasmodium of physarum polycephalum, sds - polyacryl amide gel electrophoresis ( sds - page ), western blotting, the cell - free system and optics microscopy. the major results and conclusions are as follows : 1

    本實驗以多頭絨泡菌原團為材料,採用同步化培養、細胞提取、 sds - page 、免疫印跡、非細胞體系構建、光學顯微鏡觀察等方法,研究了有絲分裂前期內肌動體構建的影響。
  7. Tissue sections from every animal were double - labeled with the antibodies of map - 2, cox - 2, gdnf, caspase - 3 and either the neuron - specific antibody neuronal nuclear protein ( neun ) or the astroglial - specific marker glial fibrillary acidic protein ( gfap ). we carried out a series of research to explore the effects and mechanism of map - 2, cox - 2, gdnf, caspase - 3 during tbi and trie d to provide some useful theory basis for both the treatment of tbi in the practice and forensic medicine

    並通過上述指標分別與神經元特異性標志物神經元( neuronalnuclearprotein , neun )和星形膠細胞特異標志物膠纖維酸性( glialfibrillaryacidicprotein , gfap )進行免疫組織化學雙,探討腦損傷后神經元及神經膠細胞反應性變化情況及其分子生物學機制,以期為腦損傷研究提供有益的數據材料,也為以上指標在法醫學實際檢案的應用提供必需理論依據。
  8. In order to avoid the possible contamination of the cytosolic actin, we ultilized a cell - free system to study the effect of nuclear actin on the process of chromosome construction

    細胞中的肌動可能參與了內的一些重要的生理活動,如骨架維持、集縮和rna轉錄等。
  9. Cultured epithelial cell undergoing division. this cell is in prophase of mitosis. microtubules are shown in green, actin is in red and mitotic chromosomes are colored blue

    以上兩圖為正處于有絲分裂前期的動物上皮細胞。綠的是微絲,紅為肌動高度螺旋成為粗短的體(藍) ,仁逐漸解體,體不規則地分佈於細胞內。
  10. This study we acquired the coding region of hcv ns5b gene by pcr of hcv full length genome and construct the recombinant plasmid pegep n3 - ns5b ; with the different concentration of g418 in the culture medium, we think the selection concentration of g418 for hepg2 cell is 800 g / ml ; the recombinant plasmid was transfected into hepg2 cell by lipofectamine2000 cells containing stable transformants were selected by the ability of resistance to g418 and isolated with the limited dilution. the stably transfected cell line expressing ns5b - egfp fusion protein was obtained by the detection under fluorescence microscope and rt - pcr

    本研究首先從hcv基因組中擴增出nssb基因,構建了nssb基因與報告分子egfp (增強型綠熒光)基因的融合基因真表達粒pegfpn30 ;通過含有不同g418濃度梯度的培養液培養hepgz細胞,確定了篩選用g4181作濃度為800pg ml ;利用脂體法將該重組粒轉hepgz細胞,經過有限稀釋法和g4壓力選擇,應用熒光顯微鏡和rtpcr檢測,獲得可穩定表達nssbegfp融合的hepgz細胞克隆。
分享友人