staining analysis 中文意思是什麼
staining analysis
解釋
染色分析-
Following laser exposure, the samples were fixed in 4 % glutaraldehyde and sent for histologic study using eosin - staining techniques for subsequent analysis with light microscopy
在激光照射之後，樣本固定在4的戊二醛中，曙紅染色後用光顯微鏡分析進行組織學研究。 -
Use pi staining of fixed cells and facs analysis to determine type of u 2 - os cell death induced by bfgf
採用固定后細胞pi染色流式細胞術檢測bfgf誘導u2 os細胞死亡的形式。 -
This gene, artificially put under the control of camv 35s, was introduced into tobacco with the aid of agrobacterium, and the transgenic plants obtained were identified by gus staining, pcr and southern blot analysis
將arge與組成型啟動子camv35s相連，構建植物表達載體，通過農桿菌介導轉化煙草。經過gus染色、 pcr及southern鑒定獲得了轉基因植株。 -
Histochemical staining in tl transgenic tobaccos showed that sigp1 promoter was not only organ - specific ( especially expressed in leaves and guard cells ), but also highly inducible by multi stress treatment such as drought, aba, high salinity and low temperature. quantitative analysis showed that gus activity in roots was very weak and no great changes were observed after treatment
通過對t1代轉基因苗的組織化學定位表明，該啟動子驅動的gus基因在逆境（如乾旱、 aba 、高鹽和冷）脅迫的葉片中表達，根中不表達，且老葉中的表達量高於幼葉中的表達量，說明其表達受發育階段的調控。 -
Test methods for analysis of lead in pvc taken from insulation and sheath of electric and optical fibre cables - method a : total lead content determination with flame excitation atomic absorption spectrometry - method b : qualitative analysis of lead by lead sulphide staining
聚氯乙烯絕緣和護套光電纖維電纜鉛分析的試驗方法.方法a :用火焰激發原子吸收光譜測定法測定法含鉛總量測定.方法b :硫化鉛斑漬中鉛的定性分析 -
Routine staining and microscopic analysis of fixed smears
常規的固定塗片染色程序及顯微鏡分析； -
Their frequencies of gus expression in pollens were 97. 755 % 0. 800 % and 96. 556 % 0. 600 % respectively. to verify these results, the self - pollinated progenies of these two putative homozygotes were examined in t2 by histochenmical gus staining of vegetative tissues and pcr analysis using specific primers
（ 2 ）通過對轉基因t1代的花粉gus基因表達檢測，快速鑒定和篩選得到了番茄純合植株，加速了純合體篩選的進程，證明此方法可靠，而且不會造成大量寶貴材料的浪費。 -
In the process of library construction, some technical details were studied, such as the combination of dna silver staining with rd technique, purification of pcr product, storage of the data about probes and bioinformatics analysis of one est, etc. 2
在文庫構建過程中，對其中的一些技術細節，如在dna銀染與rd技術結合、 pcr產物純化、探針數據的管理、 est的生物信息學分析等方面進行了探索。 -
Statistical analysis was performed to determine the relationship between staining of denture and the above factors
採用統計學方法，分析全口義齒著色與上述因素的關系。 -
Fibre furnish analysis of paper, board and pulps - guide to staining
紙紙板和紙漿的纖維配料分析.第2部分:染色指南 -
After silver staining, the 2de image analysis by imagemaster 2de software had detected 800 + 50 spots in e18. 5 pancreas map and 1000 + 50 spots in adult pancreas map, of which 8 spots increased and 20 spots decreased in quantity
用imagemaster （ pharmacia公司）圖像軟體分析，發現1000 50個蛋白質點在成年胰腺中檢測到表達， 800 50個蛋白質點在胚胎18 . 5天胰腺中檢測到表達，其中8個蛋白質點在成年胰腺組織中含量降低， 20個蛋白質點含量增加。 -
Glycoprotein bands recovered were detected by gelcodeglycoprotein staining kit, and the result showed that recovery rate reached 50 percent, that the quantity of glycoprotein once purified from sds - gel, was enough to be used in ms, hplc, protein sequence analysis, glycan analysis, and characterization so on
從sds膠上純化的茶樹葉糖肽鑒定結果看，茶樹葉糖蛋白的sds膠上純化回收率達50左右。 -
Anti - en antibody staining and in situ hybridization on oxt glc embryo using wg antisense probe showed defective en protein and defective wg transcripts bands. the embryonic analysis results indicated that the disruption of oxt gene would lead to the disruption of wg transcription and the expression of engrailed gene, as the wg transcription is dependant on the engrailed
通過對oxt生殖系克隆胚胎進行的抗en抗體染色和wg反義探針a雜交結果表明，與野生型果蠅的胚胎相比， en蛋白和wg轉錄物條帶都出現了明顯的缺失。 -
Methods : the effects of different neurotrophic factors on the growth and differentiation of neural stem cells were observed by cells counting and immunofluorescence staining. the levels of rara mrna and rxra mrna in differentiated neural stem cells were assayed by rt - pcr. agarose gel electrophoresis and image analysis
方法應用細胞計數和免疫熒光細胞化學法，研究不同神經營養因子對神經幹細胞增殖及分化的影響；應用rt - pcr 、瓊脂糖凝膠電泳和紫外分光圖象分析法檢測神經幹細胞分化過程中rar和rxr mrna表達量的改變。結果1 -
Value of cd45 and pi staining method in identifying malignant from benign pleural effusion by dna analysis
倍體分析在良惡性胸腔積液鑒別診斷中的意義 -
In the present experiment studies, an acute traumatic model of lateral cortical impact was employed to study expressive changes of microtubule associated protein - 2 ( map - 2 ), cyclooxygenase - 2 ( cox - 2 ), glial cell line - derived neurotrophic factor ( gdnf ), caspase - 3 mrna and protein after brain injury in rats. immunocytochemical staining, western blotting, nucleic acid in situ hybridization with an oligonucleotide probe and computer image analysis were used to detect the dynamic changes of map - 2 mrna, cox - 2 mrna, gdnf mrna, and caspase - 3 mrna in the cortex after moderate traumatic brain injury ( tbi )
本實驗從自行設計大鼠腦損傷落體打擊器開始，先行建立了一個便於觀察和施加處理因素、控制性好、重復性好的動物模型，選用30g擊錘從25cm高處下落，沖擊應力d為355 . 09kpa ，打擊大鼠右頂部，造成中等程度的閉合性腦損傷，從病理形態學、組織超微結構觀察及微管相關蛋白- 2 （ microtubuleassociatedprotein2 ， map - 2 ） 、環氧合酶- 2 （ cyclooxygenase2 ， cox - 2 ） 、膠質源性神經營養因子（ glialcellline - derivedneutrophicfactor ， gdnf ） 、 caspase - 3基因及蛋白表達的時間性變化，詳盡系統地闡述腦損傷后各指標變化的時間規律性及表達差異可能的形成機制。 -
Sds - page and activity staining analysis revealed that all of clones 2, 5 and 9 exhibited a single active band with 83 - kd in size, whereas clone 3 exhibited four different bands with 64 kd, 70kd, 76kd and 83 kd after construcing a series of deleted subclones from the plasmid prepared from clone - 5, a complete nucleotide sequences comprising of 3, 205 bps wes determined. one open reading frame ( orf ) was found in this sequence, which was comprised of 2, 661 bps and could encode a polypeptide with 887 amino acid residues
利用基因分析軟體genetyx對clone - 5質粒的核苷酸序列進行分析，並搜索日本dna數據庫（ dnadatabankofjapan ，簡稱ddbj ） ，推斷clone - 5質粒的幾丁質酶基因含有一個2 ， 261bp的開放閱讀框（ orf ） ，編碼一條887個氨基酸的幾丁質酶蛋白； orf上游有一個啟動子。 -
All rats were killed on the 15th day. six samples of heart were chosen from each group for examining expressions of vegf, bfgf and the coagulation factor under light microscopy by immunohistochemical staining, and the quantitative analysis on positive responsive intensity of vegf and bfgf was conducted on the other 4 heart samples using the image analysing system, then mean microvessel density mmvd was calculated
術后第15天處死大鼠，每組選取6隻心臟標本，應用免疫組化法，光鏡下觀察大鼠心肌細胞vegf bfgf及因子表達情況應用圖像分析系統定量分析vegf及bfgf陽性反應強度，計算平均微血管密度mmvd 。
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