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glycerophosphate相关的网络例句

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与 glycerophosphate 相关的网络例句 [注:此内容来源于网络,仅供参考]

The osteoblasts at 1×105/ml,2×105/ml and 5×105 /ml cell density were cultured in the DMEM medium and in the DMEM medium supplemented with β-glycerophosphate sodium and ascorbic acid.

实验选用了1×105个/ml、2×105个/ml、5×105个/ml三个不同的细胞接种浓度,并且每个浓度组分别给予含β-甘油磷酸钠和维生素C的条件培养液以及常规培养液进行细胞培养。

First passage of human amniotic epithelial cells were inoculated at a density of 1×108/L and cultured in medium containing fetal bovine serum of 0.1 volume fraction, 100 nmol/L dexamethasone, 50 mg/L ascorbic acid and 5 mmol/L β-glycerophosphate.

取第1代人羊膜上皮细胞,设立两组:诱导组以1×108 L-1密度接种于培养皿内,24 h后更换为含体积分数为0.1的胎牛血清、 100 nmol/L地塞米松、50 mg/L抗坏血酸、5 mmol/Lβ-甘油磷酸的诱导培养液。

osteoblasts at 1×105/ml,2×105/ml and 5×105 /ml cell density were cultured in the DMEM medium and in the DMEM medium supplemented with β-glycerophosphate sodium and ascorbic acid.

实验选用了1×105个/ml、2×105个/ml、5×105个/ml三个不同的细胞接种浓度,并且每个浓度组分别给予含β-甘油磷酸钠和维生素C的条件培养液以及常规培养液进行细胞培养。

Objective To investigate whether osteoblasts cultured in vitro can form mineralization nodes. Method The osteoblasts at 1×105/ml,2×105/ml and 5×105 /ml cell density were cultured in the DMEM medium and in the DMEM medium supplemented with β-glycerophosphate sodium and ascorbic acid.

目的 了解体外培养成骨细胞的接量对钙化结节形成的影响方法实验选用了1×105 /ml、2×105个/ml、5×105个/ml三个不同的细胞接种浓度,并且每个浓度组分别给予含β-甘油磷酸钠和维生素C的条件培养液以及常规培养液进行细胞培养。

Thermo-sensitive neutral systems based on a chitosan/ glycerophosphate salt complex were prepared.

采用壳聚糖与甘油磷酸盐分子组装的原理制备了具有温敏性的配合物凝胶体系,其在室温下呈液态,升温凝胶化。

METHODS:Calcification of cultured rat VSMCs was produced by incubation with β-glycerophosphate. Calcium content, Ca2+ deposition and alkaline phosphatase activity were analyzed to estimate the extent of calcification.

目的:在离体钙化的血管平滑肌细胞上,观察内皮素受体阻断剂对血管平滑肌细胞钙化的影响,探讨内皮素促进细胞钙化的信号转导和分子机制。

Methods The osteoblasts at 1×105/ml,2×105/ml and 5×105 /ml cell density were cultured in the DMEM medium and in the DMEM medium supplemented with β-glycerophosphate sodium and ascorbic acid.

实验选用了1×105个/ml、2×105个/ml、5×105个/ml三个不同的细胞接种浓度,并且每个浓度组分别给予含β-甘油磷酸钠和维生素C的条件培养液以及常规培养液进行细胞培养。

Objective To evaluate the feasibility of the injectable thermosetting chitosan and glycerophosphate gel as tissue engineering scaffold by observing its biocompatibility and survival ability of BMCs encapsulated in the gel.

目的观察温固化可注射性壳聚糖/甘油磷酸钠凝胶的组织与细胞相容性,评估其作为组织工程支架的可行性。

Results There were more mineralization nodes to form in shorter time in the 1×105/ml cell density group compared with in the 2×105/ml cell density group, but in the 5×105/ml cell density group, there were not, and with the DMEM medium contained β-glycerophosphate sodium and ascorbic acid, mineralization nodes formed more early compared with the DMEM medium.

结果 在培养30天内,条件培养液或常规培养液培养的5×105个/ml组细胞无结节形成;而2×105个/ml组和1×105个/ml组都有钙化结节形成,而且有细胞越少形成结节越早,数量越的趋势;给予条件培养液又较常规培养液培养有结节形成早而多的趋势。

On the 1st and 7th days, supernatant was derived from cells in primary culture to measure content of β-glycerophosphate disodium with chemiluminescence technique.

取原代培养细胞1和7 d时的上清液,用化学发光法测定β-HCG含量。

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