查询词典 safranine

RESULTS: HE and safranine O staining both showed no cellular structure in the matrix with only recesses left by the removed cells.

软骨蛋白聚糖免疫组织化学染色阳性，提示脱细胞关节软骨基质内仍存在软骨蛋白聚糖。

Methods Safranine staining was conducted for the detection of the forming ability of biofilm in 96-well plates.icaAD,icaBC,sar,agr and sigB was amplified by PCR.

方法96孔板番红染色法检测生物膜的形成，icaAD、icaBC、sar、agr和sigB的PCR扩增，并对产物进行测序和同源性比较。

N-doped TiO2 nanotubes absorb visible light distinctly, and showed higher efficiency of photocatalytic activity than TiO2 nanotubes by model experiment of degradation of the solution of Safranine T.

结果表明，用模板法制备的二氧化钛纳米管管径均匀、可控且排向一致，从DRS光谱可以推测出氮掺杂后的二氧化钛纳米管在可见光区有较强的吸收，并且与二氧化钛纳米管相比氮掺杂的二氧化钛纳米管的降解碱性藏花红溶液的效率更高。

In pH value 6.40 Clark-Lubs buffer solution, the fluorescence intensity of safranine T and sodium dodecyl benzene sulfonatewas determined. After adding organophosphorus pesticides, the fluorescence intensity was determined. Based on this, a new fast and simple method for determination of the organophosphorus pesticides total-residues was developed.

方法］在pH值6.40的Clark-Lubs缓冲溶液中，加入碱性藏花红与一定浓度的十二烷基苯磺酸钠，测定荧光强度，再加入有机磷农药，检测荧光强度变化，据此建立测定有机磷农药残留总量的新方法。

Three group male sterile and maintenance lines of monogerm sugar beet as materials were used, we observed the biological characters of their buds, anthers and anther structure, and the development process of pollens by the methods of conventional Paraffin Slicer, Safranine Ai-Shi Haematine Crystal and Fast Green.

方法］以3对单胚型甜菜雄性不育系和保持系为试验材料，采用常规的石蜡切片方法，对花蕾和花药的生物学特性以及花药结构、花粉发育过程进行比较。

Peptide Nucleic Acids; Safranine T ; Fluorescence Quenching ; PNA-DNA Twin Spirochaeta.

肽核酸；藏红T ；荧光猝灭； PNA-DNA双螺旋

METHODS: In the experimental group, ADSCs were cultured with the scaffold and induced by CDMP1(50 μg/L) in basic medium for another 2 weeks. In the control group, SD rat cartilage cells were cultured with elementary nutrient liquid with scaffold for another 2 weeks. Twenty nude mice were imbedded the composite of cells-scaffold of the experimental group in their left armpits and the composites of cells-scaffold of the control group in right armpits. Every ten nude mice were killed at 8 and 12 weeks and were examined by safranine O-fast green and toluidine blue staining.

体外培养的脂肪干细胞复合于支架上，加入诱导液(基础培养液+ 50 μg/L软骨形态发生蛋白1)继续培养2周作为实验组；将SD仔鼠软骨细胞复合于支架上，常规培养2周作为对照组。20只裸小鼠，左侧腋窝皮下均植入实验组细胞-支架复合物，右侧腋窝皮下均植入对照组细胞-支架复合物。8， 12周各处死10只，行甲苯胺蓝和番红O-固绿染色。

A new parallel-epiphyseal cartilaginous tissue was found in the subcutaneous tissue 4 weeks after operation. The tissue was stained with HE, toluidine blue, safranine O and collagenⅡ. A large number of chondrocytes and a cartilage lacuna-like structure were observed under a microscope with no obvious inflammatory reaction around the calcium alginate and polylysine microspheres.

结果 体外培养时微球中骺板细胞生长、增殖情况良好；移植皮下后第4周取材可见外形呈类骺软骨样组织块，行HE、甲苯胺蓝、番红"O"及Ⅱ型胶原等染色，镜下观察可见大量软骨细胞及类软骨陷窝样结构，植入的海藻酸钙微球周围组织无明显炎症反应。

The cells of 2~ passage were used for proliferation kinetics studying by MTT colorimetric method.The pasagcd chondrocytes' phenotypes were as- sessed by safranine O staining and immunostaining for typeⅠ,Ⅱcollagens and aggrecan.Results For in vitro culturing of AHAC,human AB serum was superior to FBS,and the optimal concentration of human serum was 10%.But for FBS,20% was better,A similar result was got with or without the growth factors contained.

结果对于AHAC，人AB血清培养优于FBS；合适的人AB血为10%；合适的FBS浓度为20%；无血清培养细胞增殖非常缓慢；不加因子用人AB血清培养细胞梭形化明显，加用生长因子后与使用FBS在形态上一致。

The opti mumreagent,which was selected out through comparing the staining effects of 4 staining reagents(I-IK coloration solution,improved phenol fuchsin,safranine staining solution and aceto carmine),was i mproved phenol fuchsin.

通过比较4种染色试剂(I-IK染液、改良苯酚品红、番红染液和醋酸洋红)的染色效果选出的最佳试剂为改良苯酚品红。

The labia have now been sutured together almost completely.The drains and the Foley catheter come out at the top.

此刻阴唇已经几乎完全的缝在一起了，排除多余淤血体液的管子和Foley导管从顶端冒出来。

To get the business done, I suggest we split the difference in price.

为了做成这笔生意，我建议我们在价格上大家各让一半。