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1)  3H-proline incorporation
3H-脯氨酸掺入法
1.
By culturing 1,12,24 and 48 h after the irradiation,the synthesis of collagen was measured by 3H-proline incorporation determination.
于照射后不同时间段,采用3H-脯氨酸掺入法分别两组细胞胶原合成情况。
2)  [3H]leucine intake method
[3H]标记亮氨酸掺入法
1.
Methods Using cultured neonatal rat cardiomyocytes treated with different factors as a model,surface area of cardiomyocytes was measured by computer photograph analysis software;the protein synthesis rate was assayed with leucine intake method;the proto-oncogene c-fos protein expression was assessed with immunocytochemistry technique;the markers of cardiom.
方法以培养的乳鼠心肌细胞为模型并分组给药,用计算机图像分析软件测量心肌细胞表面积,[3H]标记亮氨酸掺入法测定心肌细胞蛋白质合成速率,免疫细胞化学方法检测心肌细胞原癌基因c-fos蛋白表达,半定量RT-PCR检测心肌细胞肥大特征性胚胎型基因β-肌球蛋白重链(β-MHC)、α-骨骼肌肌动蛋白(α-skA)和心房肽(ANP)的mRNA表达。
3)  3H-proline
3H-脯氨酸
4)  [ 3H] proline
[~3H]脯氨酸
5)  ~3H-TdR incorporation
3H-TdR掺入法
1.
Cadmiumly-induced proliferation suppression of peripheral blood mononuclear cells in Carassius auratus by ~3H-TdR incorporation test;
~3H-TdR掺入法检测镉致鲫外周血单个核细胞的增殖抑制
2.
Correlative study of proliferation of aorta smooth muscular cells by using flow cytometry and ~3H-TdR incorporation in rats;
流式细胞术法与~3H-TdR掺入法观察细胞增殖的相关性研究
3.
Objective To study the best suitable condition of SMMC-7721 hepatocarcinoma cell in drug sensitivity test using the ~3H-TdR incorporation.
目的探讨3H-TdR掺入法在进行SMMC-7721系细胞肿瘤药敏试验实验时的最佳实验条件。
6)  3H-TdR incorporation
3H-TdR掺入法
1.
The proliferative responses of T cells were determined by 3H-TdR incorporation assay and the analysis of epitopes on peripheral blood T cells was undertaken with flow cytometry.
逐日观察细胞的生长状态并绘制生长曲线,用3H-TdR掺入法分析PBTC的增殖效应,用FITC标记的单抗经流式细胞仪(FCM)分析细胞CD3、CD4、CD8、CTLA-4、4-1BB及OX40的表达。
2.
Objective: To explore the best suitable experiment condition used to compare the MTS colorimetry and the 3H-TdR incorporation.
目的:确定MTS比色法与3H-TdR掺入法在进行实验比较时的最佳实验条件。
补充资料:L-丙氨酰-L-脯氨酸
分子式:C8H14N2O3
分子量:186.21
CAS号:13485-59-1

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