后茜素

基本解释 (translations)

hystazarin

与后茜素相关的网络例句 [注：此内容来源于网络，仅供参考]

Mineralized matrix was determined by Alizarin Red S staining at 16 and 22 days after culture.

茜素红染色后显微镜下观察培养16，22 d 矿化结节形成。

Alizarin red staining results showed that the calcified nodules were produced after induction.

茜素红染色结果表明，诱导后出现钙化结节。

After 20 d calcium induction, jacinth calcium salts could be detected in the cells by alizarin red staining.At day 10 after being adipoinduced, the cells showed positive oil red O staining.

结果：成功获得了稳定表达GFP的ADSCs，GFPADSC经成骨诱导20 d后茜素红染色可见有橘红色钙盐沉积；经成脂诱导10 d后油红O染色阳性。

After 20 d calcium induction, jacinth calcium salts could be detected in the cells by alizarin red staining.At day 10 after being adipo induced, the cells showed positive oil red O staining.

结果：成功获得了稳定表达GFP的ADSCs，GFP ADSC经成骨诱导20 d后茜素红染色可见有橘红色钙盐沉积；经成脂诱导10 d后油红O染色阳性。

The adipoinduced MSCs were detected with oil red O staining. RESULTS: ADSCs, stably expressing GFP, were obtained successfully from the transgenic mice with GFP gene. After 20 d calcium induction, jacinth calcium salts could be detected in the cells by alizarin red staining.

结果：成功获得了稳定表达GFP的ADSCs，GFPADSC经成骨诱导20 d后茜素红染色可见有橘红色钙盐沉积；经成脂诱导10 d后油红O染色阳性。

In 10.5 day mouse embryo, by the induction of notochord, mesenchymal cells of ventromedial somite differentiate into sclerotome, cells migrate towards notochord, forming perinotochord tube around notochord, the cartilage is till invisible, alcian dying is faintly positive.

椎体区域发生骨化后（E16.5），阿利辛兰染色呈阴性，茜素红染色呈阳性，仅有Ihh在椎体边缘有表达，无PTHrP表达；在椎间盘区域，仍然保持阿利辛兰染色阳性，仅有PTHrP的表达，无Ihh表达。

The iliac bone defect moulds were prepared and the compound scaffolds were implanted. The compound scaffolds were taken out after four and eight weeks separately, bone healing status and appearance of scaffolds were observed by eyes, the osteoplast growth status in compound scaffolds were viewed by HE and chinalizarin dyeing separately, the degradation of the compound scaffolds in vivo were observed by SEM.

制作髂骨骨缺损模型，在骨缺损处植入骨支架复合体，植入后4周、8周取材大体观察材料与周围骨愈合情况，HE染色及茜素红染色观察支架复合体内成骨细胞生长及扫描电镜观察支架体内降解情况。

After osteoplastic induction, peripheral blood MSCs had strongly positive reactions for alkaline phosphatase staining, total collagen staining, alizarin red staining.

外周血间充质干细胞成骨诱导后，碱性磷酸酶染色、总胶原染色及茜素红染色均呈强阳性；成脂诱导后油红染色呈阳性，有一定数量的脂滴形成。

The experimental group corneas were preserved by organ culture for 4 weeks, the corneal thickness was measured with ultrasonic corneal pachymeter. Then every corneas were divided into half -chip, there are 48 half-chip total. It was divided into 4 groups, there are 12 half-chip in every groups. The corneal endothelial cell density of 12 half-chip were counted through Alizarin Red-Trypan blue staining; 12 half-clip corneas were fixed with 4% neutral formalin solution, HE staining was performed, the expression of AQP-1 in corneal stroma and corneal endothelial cell were detected through immunohistochemical staining; Na~+-K~+-ATPase activities in 12 half-clip corneas were examined with Na~+-K~+-ATPase kit; the expression of AQP-1 mRNA were detected through real-time fluorescent quantitation PCR.

实验组经器官培养保存4周后以角膜测厚仪测量角膜厚度，然后每个角膜被分成两半，共48个半片角膜，再分成4组，每组12个半片。12个半片用茜素红-台盼蓝染色染色行角膜内皮细胞计数；12个半片角膜用4%中性福尔马林溶液固定行HE染色、应用免疫组化染色检测AQP-1在角膜基质和内皮细胞表达的改变；12个半片角膜用Na~+-K~+-ATP酶试剂盒测量角膜内皮细胞Na~+-K~+-ATP酶活性；12个半片角膜用实时荧光定量PCR检测AQP-1mRNA表达改变。

The general situations of the eye were observed and the corneal thickness were measured with ultrasonic corneal pachymeter after the animal models was established. After a week, the corneas were removed after the experimental animals are put to death. The corneal endothelial cell density of 12 half-chip were counted through Alizarin Red-Trypan blue staining; 12 half-clip corneas were fixed with 4% neutral formalin solution , HE staining was performed, the expression of AQP-1 in corneal stroma and corneal endothelial cell were detected through immunohistochemical staining; Na~+-K~+-ATPase activities in 12 half-clip corneas were examined with Na~+-K~+-ATPase kit; the expression of AQP-1 mRNA were detected through real-time fluorescent quantitation PCR.

术后观察眼球大体情况、测量角膜厚度。1周后处死实验动物取角膜，用茜素红-台盼蓝染色染色行角膜内皮细胞计数；用4%中性福尔马林溶液固定行HE染色、应用免疫组化染色检测AQP-1在角膜基质和内皮细胞表达的改变；用Na~+-K~+-ATP酶试剂盒测量角膜内皮细胞Na~+-K~+-ATP酶活性；实时荧光定量PCR检测AQP-1mRNA在角膜内皮细胞表达的改变；并于正常对照组角膜比较。