Total RNA was extracted from hepatic cells of mouse.
从小鼠肝脏细胞中提取总rna。
Two total RNA extraction methods were developed firstly.
建立了两种木本植物总rna的提取方法。
Tissue, Total RNA, Human Disease, Alzheimer's Disease, Occipital Lobe.
组织，总rna，病人，老年性痴呆，顶叶。
Tissue, Total RNA, Human Disease, Alzheimer's Disease, Precentral Gyrus.
组织，总rna，病人，老年性痴呆，中央前回。
Tissue, Total RNA Matched Pairs, Human Primary and Metastasis Tumor, Stomach.
组织，总rna配对，人原发性和转移肿瘤，胃。
Tissue, Total RNA Matched Pairs, Human Primary Tumor, Metastasis Tumor and Normal, Stomach A.
组织，总RNA配对，人原发性肿瘤，转移肿瘤和正常组织，胃A。
Total RNA was extracted from muscle tissue, brain tissue, gastric tissue and liver tissue of ten rabbits.
本试验以健康无病的10只比利时兔为材料，分别从兔肌肉、大脑和肝组织中提取总RNA。
With tea plant embryos as the research object, we compares and analyses several methods of total RNA extraction.
茶树种胚中富含多糖和多酚类化合物，这增加了总RNA的提取难度。
Three methods were compared in the extraction of total RNA from Birch leaves. CTAB methods were the ideal for the trees?
比较了三种树木RNA的提取方法，确定改良的CTAB法为白桦组织RNA的最优的提取方案。
In this paper, a modified hot phenol method was applied to extract total RNA from white tea leaves and non-green tissues.
本文尝试利用改良热酚法提取白茶和非绿色组织的总rna。
METHODS Total RNA was extracted from human embryonic lung fibroblast cells (WI 38) and the whole length gene of human OPG was obtained by RT PCR.
方法从培养的人胚肺成纤维细胞(WI- 38)中提取总rna，经rt -PCR获得人破骨细胞抑制因子基因。
Methods On the Day 17 after being infected with Trichinella spiralis, pre encysted larvae were collected and total RNA of the larvae was obtained.
方法大鼠感染旋毛虫后第17天收集成囊前期幼虫，提取虫体的总rna。
The method could produce cotton total RNA with higher purity and integrality in a shorter time from different tissues of cotton than other conventional methods.
该方法与异硫氰酸胍法或冷酚法等相比具有更简便、得到的棉花组织总rna完整性好和纯度高等优点。
Methods the total RNA was extracted from Z37 virus infected cells and the RT-PCR products were cloned into t vector, sequenced and analyzed by DNASTAR software.
方法设计出针对各片段的特异性引物，用P CR方法从Z 37病毒感染的细胞提取细胞总rna，逆转录扩增、产物克隆t载体，纯化后测序，测定的序列应用DNASTAR软件比较分析。
Methods the total RNA were prepared from Z10 virus infected cells and the RT PCR product was cloned into t vector, sequenced and analyzed using DNASTAR software.
方法从Z 10株病毒感染的细胞提取总rna，将逆转录pcr扩增的产物纯化后克隆于t载体并进行序列测定，应用dnastar软件分析比较。
Methods the total RNA were prepared from Z10 virus infected cells and the RT PCR products was cloned into t vector, sequenced and analyzed by using DNASTAR software.
方法从Z 10病毒感染的细胞提取总rna，将逆转录聚合酶链反应(RT PCR)扩增的产物纯化后克隆于t载体并进行序列测定，应用dnas TAR软件分析比较。
The invention employs RT-PCR method, extracts sequence 1 from total RNA of tentacles of sagartia rosea ( sequence 1 indicates), the protein coded by the gene( sequence 2 indicate).
本发明用RT-PCR的方法，从玫瑰红绿海葵触手总RNA中分离得到的1序列所示。该基因编码的蛋白（重2序列所示。
This review summarized the recently research process of Sq RT-PCR. It including extraction of total RNA, primer design, definition of cycle count, selection of inner reference and so on.
该文就半定量RT-PCR法的检测步骤及技术的关键因素（总RNA提取、引物设计、循环数的确定和内参的选择等）进行综述。
The swim-up method was adopted to purify the spermatozoa from possible contamination of somatic cells and the spermatozoa total RNA extracted by Trizol was used for SAGE library analysis.
混合所有总RNA进行基因表达系列分析（SAGE），随后对所得SAGE文库进行功能聚类性分析。
INTERVENTIONS: Tissues of edema area and normal brain of 40 rats were collected in different time after damage: total RNA were abstracted and MMP-9 gene expression was tested by PCR means.
干预：40只大鼠，于伤后不同时间取水肿区脑组织及正常脑组织：提取组织总rna：用共扩增反转录定量pcr方法测定MMP - 9基因表达水平。
Objective:To observe the ability of DC vaccine transfected with tumor cell total RNA to induce specific antitumor immunity in vitro and the primary clinical application in Ewing sarcoma patients.
目的：探讨尤文肉瘤细胞总RNA转染的DC疫苗体外诱导特异性抗肿瘤免疫的能力及临床初步应用的效果。
Total RNA from each sample was isolated and biotin-labeled probes were hybridized to the human genome U133A chip, after which the chip was washed and scanned. Data were analyzed using DMT software.
从各个样本中提取总rna并制备成辅酶r标记的探针和人基因组u 133a芯片杂交，提取和分析数据。
Total RNA from each sample was isolated and biotin-labeled probes were hybridized to the human genome U133A chip, after which the chip was washed and scanned. Data were analyzed using DMT software.
从各个样本中提取总rna并制备成辅酶r标记的探针和人基因组u 133a芯片杂交，提取和分析数据。
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