免疫印迹杂交结果显示MYOG和MYOD的蛋白质表达水平也发生了与基因表达相一致的变化。
The results of Western blotting showed that protein expression levels of MYOG and MYOD also changed as same as the gene expression levels.
蛋白质表达水平的成功定量很大程度上依赖于由2de分析软件提供的斑点匹配、归一化和背景减除算法。
Successful quantification of protein expression levels is largely dependent on the algorithms for spot matching, normalization, and background subtraction provided by the 2de analysis software.
应用免疫组化s - P法检测24对食管癌组织及相应正常食管组织中抑癌基因pten的蛋白质表达水平。
Expression levels of PTEN gene were detected by the SP immunohistochemical technique in the selected 24 pairs of tumor tissues and the related normal tissues.
结论：FCM是检测膀胱癌多药耐受蛋白质表达水平和MRP功能水平的好方法，DNR是FCM检测MRP功能的良好探针。
Conclusions: FCM is a good method to detect MDR protein and MRP function of bladder carcinoma, and DNR is a good probe to detect MRP function by FCM.
通过这些技术，可以从分子水平探索营养素对基因和蛋白质表达的影响，也可以反观基因改变对营养相关性疾病发生的影响。
These technologies made it possible to study the influences of nutrients on gene and protein expression, and reversely, the influences of gene changes in nutrient related disturbances in metabolism.
蛋白质磷酸化和去磷酸化作为原核和真核细胞表达调控的关键环节，了解其对功能的影响可以深入理解生命系统在分子水平的调控状况。
As the key point of expression modulation in prokaryotic and eukaryotic cells, the protein phosphorylation and dephosphorylation may help reveal the status of the life system at the molecular level.
它主要提供染色质水平上控制植物基因表达的蛋白质信息。
It focuses on the proteins that control plant gene expression at the chromatin level.
通过家蚕各个时期胚胎蛋白质的研究，可以从蛋白质水平探讨胚胎蛋白质的构成和基因顺序表达的规律。
The composing of embryo proteins and rule of gene sequential expression at protein level can be discussed by researching the proteins of every embryo development stage of silkworm.
表达的昼夜节律时钟的基因和部分脂联素代谢途径的肝脏是测试的RNA，蛋白质，或酶活性水平。
The circadian expression of clock genes and components of adiponectin metabolic pathway in the liver was tested at the RNA, protein, or enzyme activity level.
细胞微阵列可广泛用于DNA、RNA和蛋白质水平上的基因原位表达研究。
The cell microarrays could be widely used the in situ analysis of the gene expression at the DNA, RNA, and protein level.
目的：探讨人胚胎滋养层细胞中染色体数目异常与着丝粒特异性蛋白质CENP-I表达水平的相关性。
Objective:To observe the expression level of CENP-I gene in human trophoblast cells with numerical chromosomal aberration.
目的：探讨人胚胎滋养层细胞中染色体数目异常与着丝粒特异性蛋白质CENP-I表达水平的相关性。
Objective:To observe the expression level of CENP-I gene in human trophoblast cells with numerical chromosomal aberration.
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