金膠體 的英文怎麼說

中文拼音 [jīnjiāo]
金膠體 英文
gold colloid
  • : Ⅰ名詞1 (金屬) metals 2 (錢) money 3 (古時金屬制的打擊樂器) ancient metal percussion instrum...
  • : Ⅰ名詞1 (某些具有黏性的物質) glue; gum 2 (橡膠) rubber 3 (姓氏) a surname Ⅱ動詞(用膠粘) st...
  • : 體構詞成分。
  1. Localization of specific glycoproteins of sperm cell membrane from

    玉米精細胞質膜特異糖蛋白免疫定位
  2. Development of the dipstick of gold - immuno chromayography assay for the diagnosis of plague

    鼠疫法快速診斷試劑盒的研製
  3. Our study results indicated : on light adaptation, the ratios of the density of the gold particles in the rhabdom to that in the cytoplasm in macrobrachium rosenbergi photoreceptor cell in high calcium solution, physiological solution and low calcium solution was 21 / 6 、 1

    結果顯示:光適應組,在高鈣溶液、生理溶液和低鈣溶液中細胞質與感桿束中密度的比值是21 / 6 、 17 / 8和13 / 14 。
  4. In our experiment, after light and dark adaptation, the retina of the macrobrachium rosenbergi was respective incubated in high calcium solution, physiological solution and low calcium solution. we studied the effect of calcium concentration on the content and subcellular localization of gq protein a subunit in the photoreceptor cell of macrobrachium rosenbergi on light adaptation and dark adaptation by sds - page technology and imunoelectron microscopy technology. our study results indicated : 一 、 effects of calcium concentration on the soluble gq protein a subunit in the photoreceptor cell of macrobrachium rosenbergi on light adaptation and dark adaptation

    而鈣離子對gq蛋白亞基活性有無影響還未見報道。我們以光適應和暗適應條件下的羅氏沼蝦復眼視網膜為材料,分別用高鈣溶液、生理溶液、低鈣溶液孵育后,通過sds ? page電泳技術及免疫電鏡技術,研究鈣離子濃度對光暗適應時羅氏沼蝦感光細胞gq蛋白亞基含量的影響及亞基亞細胞定位的影響。
  5. Ip3 - ip3 receptor ( ip3r ) interaction mediates the release of ca2 + from the endoplasmic reticulum in response to many different extracellular stimulus. for higher plants, however, though it is now generally accepted that ip3 participates in signal transduction in many important cellular processes, only limited evidence is available for the presence and properties of the ip3r - like protein so far. here, using the immunological methods with an antibody raised against a mammalian inositol 1, 4, 5 - triphophate receptor ( type 1 ), we found that, 1 ) the antibody across - reacted the proteins with about 200kd in microsomes from oryza sativa and about 200kd from arabidopsis thaliana respectively

    本實驗用sds - page電泳和免疫印跡的方法,用哺乳動物大鼠三磷酸肌醇受的多肽做抗對類三磷酸肌醇受蛋白鑒定,結果表明:抗與水稻和擬南芥微粒蛋白分子量大約為200kd的蛋白交叉反應,同時還發現在水稻微粒蛋白62kd和擬南芥微粒蛋白45kd處有交叉反應的蛋白條帶存在,表明在植物中有類三磷酸肌醇受蛋白的存在;用免疫方法,發現類三磷酸肌醇受蛋白主要分佈於液泡膜和細胞質膜上。
  6. Detection of clenbuterol hydrochloride in urine colloidal gold immunochromatographic method

    尿液中鹽酸克侖特羅的測定免疫層析法
  7. Finger clip - spo2 sensor for adults ; available weight upon 30kg ; provided plug : n12pin, ; gilded point inside the connectors ; for cables : white color, innoxious tpu, high double - shielded cable, od4. 0mm, length 3. 2 m ; new special alloy conductor increases the cable using life for 3 5 times ; finger pads : medical silica - gel, no irritability

    021成人指夾式, 3 . 2m . tpu無毒線材對人絕對無害。特殊合增加線纜壽命3 5倍。護墊:醫用硅無過敏性品質承諾:非人為損壞保修一年
  8. Finger clip - spo2 sensor for adults ; available weight upon 30kg ; provided plug : lemo 5pin, ; gilded point inside the connectors ; for cables : white color, innoxious tpu, high double - shielded cable, od4. 0mm, length 3. 2 m ; new special alloy conductor increases the cable using life for 3 5 times ; finger pads : medical silica - gel, no irritability

    插頭: lemo5pin單定向成人指夾式, 3 . 2m . tpu雙屏蔽線材保證信號傳送更清楚。特殊合增加線纜壽命3 5倍。護墊:醫用硅無過敏性品質承諾:非人為損壞保修一年
  9. Finger clip - spo2 sensor for adults ; available weight upon 30kg ; provided plug : odu 5pin ; gilded point inside the connectors ; for cables : white color, innoxious tpu, high double - shielded cable, od4. 0mm, length 3. 2 m ; new special alloy conductor increases the cable using life for 3 5 times ; finger pads : medical silica - gel, no irritability

    連接器: odu7pin 179成人指夾式, 3 . 2m . tpu無毒線材對人絕對無害。特殊合增加線纜壽命3 5倍。高性能雙屏蔽效果護墊:醫用硅無過敏性
  10. Green : the peroxisomes labeled with fitc ; blue : the dna labeled with dapi ; material : rat liver cells

    [何鍵.大鼠肝細胞過氧化物酶的免疫標記.中山大學本科生畢業論文. 2005
  11. Prior experience in performing colloidal gold particle or enzymatic - based immunoassays for the detection of human infectious diseases is desired

    有以免疫測定為基礎的或生化酶研究經驗優先考慮
  12. During the past six years, gold particles and the lateral - flow tests in which they are used have become further established in point - of - care testing

    摘要在過去的6年裡,及免疫層析試劑越來越多的被用於快速檢測上。
  13. The gold particles and virus could be seen binded together in the electronic microscope, which indicated the activity of purified igg was high. clinical application of hyperimmunalserun was used to treat dogs with clinicalsigns compatible with canine distemper and parvovitus enteritis

    將純化的igg與提純的cdv 、 cav病毒反應後分別與標記的spa結合,在電鏡下可清楚地觀察到病毒與顆粒的結合,說明提取的igg的效價、活性較高。
  14. Current research interests of our faculty members can be broadly classified into the following areas : analytical and environmental chemistry, inorganic and structural chemistry, organic synthesis, organometallic chemistry, physical and biophysical chemistry, chemistry of macromolecules and colloids, surface and materials chemistry, laser spectroscopy, theoretical and computational chemistry

    他們的研究專長包括:分析及環境化學、無機及結構化學、有機合成、屬有機化學、物理化學及生物物理化學、高分子及化學、表面及材料化學、激光光學、理論及計算化學等。
  15. Thin sections of host leaf cells infected by bbwv - 2 isolate b935, which were gold - labeled by antibodies of bbwv - 2 coat protein ( cp ) and vp37, respectively, were prepared to elucidate the locations of vp37 in cell and possible function of vp37 and cp in cell to cell movement. observation in electron microscope showed that virus particles were presented not only in cytoplasma but also in chloroplast, while vp37 was existed only in cytoplasma and associated with tubular structure through the cell wall

    為研究vp37在寄主細胞中的作用機制及其在細胞中的分佈,通過間接標記6his - vp37兔抗血清,同時還標記了病毒的外殼蛋白單克隆抗,對bbwv - 2分離物b935感染的病葉超薄切片的電子顯微鏡觀察發現:病毒粒子除了聚集在胞質中,還存在於寄主的葉綠內; vp37蛋白能在細胞壁上形成管狀結構,在胞質中亦有分佈。
  16. Reverse osmosis is in a salt water such as raw water than natural infiltration to exert greater pressure on the pressure and make the water from the high concentration side infiltrate low concentrations party to the original edema water pressure to the membrane elements on the other side into pure water and raw water minor impurities, colloid, organic matter, heavy metals, bacteria, viruses and other harmful substances and are all retained from the sewage discharge into export

    反滲透就是在有鹽份的水中如原水施加比自然滲透壓力更大的壓力,使水由濃度高的一方滲透到濃度低的一方,把原水腫的水分子壓到膜的另一邊變成純凈水,而原水中的細微雜質有機物重屬細菌病毒及其他有害物質都統統截留下來並經污水出口排放掉。由於反滲透膜的孔徑僅0 . 0001
  17. When exciting at 1064nm, the fluorescence of the crystal violet ( cv ) in the cv - au sol system will be quenched rapidly and meanwhile its raman signals will also be enhanced at least 105. after addition of some drops hno3 ( 1 + 10 - 2m ), due to the chemical interaction between some cv molecules and hno3, some hcv derivatives will be formed. compared with cv, hcv can be adsorbed on metal surface more easily and tightly so there is some extra enhancement in this condition

    結果表明,結晶紫分子?金膠體系中結晶紫分子在1064nm近紅外光激發條件下,其熒光得以大大淬滅,同時拉曼得到了至少不低於10 ~ 5倍的增強;當進一步加入硝酸使得其處于酸性氣氛下時,由於部分結晶紫分子與硝酸發生了化學作用形成了結晶紫分子的單替代衍生物( hcv ) ,而hcv與結晶紫分子相比,更容易吸附在屬表面,因此結晶紫分子nir - sers還將有很大的增強。
  18. Test method for porosity in gold or palladium coatings on metal substrates by gel - bulk electrography

    電譜法測定屬基物上或鈀塗層孔隙度的方法
  19. Standard test method for porosity in gold or palladium coatings on metal substrates by gel - bulk electrography

    用凝電譜法測定屬基物上或鈀塗層孔隙度的標準試驗方法
  20. Then using ecbp21 antibody and immunogold transmission electron microscopy method, we studied the subcellular localization of ecbp21. the results indicated that the gold particles were mainly localized in the cell wall in callus cells and rachis cells of angelica dahurica. these results indicated that ecbp21 mainly localized in cell wall, which provide a direct evidence of the extracellular existence of ecbp21. furthermore, using ecbp21 antibody and immunohistochemical method, we studied the organic specially distribution of ecbp21, the results indicated that ecbp21 distributed in all organize, but it distributed more in leave n flower rachis than in leafstalk and root

    首先,構建了ecbp21表達載,誘導了重組蛋白的表達,並通過回收法獲得了大量純化重組ecbp21蛋白,制備了高效價、高特異性抗;隨后,利用ecbp21抗,結合免疫電鏡定位技術進行了ecbp21亞細胞定位研究,結果顯示:在白芷愈傷組織細胞和花序軸細胞中顆粒主要分佈在細胞壁區域,而在細胞內未發現或僅有少量顆粒分佈,表明ecbp21蛋白主要定位於細胞壁區域,這為細胞外cambp ( ecbp21 )的胞外存在提供了直接證據:進一步,利用ecbp21抗,通過免疫組織化學分析研究了ecbp21組織特異性分佈狀況,結果表明ecbp21在白芷各組織中均有分佈,但在葉、花、花序軸中分佈較多,而在葉柄、根中分佈較少。
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