cdna
美英
- n.互补脱氧核糖核酸；反向转录脱氧核糖核酸
- 网络基因；微阵列生物晶片；文库
cdnacdna
互补脱氧核糖核酸
利用人体肝微粒体和互补脱氧核糖核酸(cDNA)表达的细胞色素P450同工酶进行的体外研究显示，硼替佐米主要通过细胞色素P4…
基因
...分子杂交技术为基础，将许多已知的、特定的寡核苷酸或基因(cDNA)片段作为探针，有序地、高密度地排列在玻璃、硅片或 …
反向转录脱氧核糖核酸
BNP 反向转录脱氧核糖核酸（cDNA）由1 900个核苷酸组成，转录起始位点在ATG上游30～60 by处，有多个 AGC重复序列。B…
微阵列生物晶片
微阵列生物晶片（cDNA），这个晶片可应用於疾病检测、新药开发与基因比对等方面，相关词： 看另一则问题 更多 其他回答 (…
文库
百科分类列表 - 价值中国网 ... competent cell —— 感受态细胞 CDNA 文库 cDNA library ——cDNA 文库 ...
编码序列
对BnCOP1 编码序列( cDNA) 演绎出的氨基酸序列分析表明，其编码的蛋白包含有N 端的环形锌指结合域( ring finger zinc bindin…
基因过表达
基因过表达（cDNA）以及shRNA的干扰序列设计、载体构建、慢病毒包装、稳定株构建全套询价。* 联 系 人： * 称 呼： * 公 …
1
Inoculate the tobacco leaf with TMV common strain, sampling in a week and withdraw the whole genome TMV-RNA, reverse it to cDNA.
用烟草花叶病毒普通株系接种烟草叶片，一周后采样提取全基因组TMV-RNA，反转录合成第一链cDNA。
2
RESULTS: The results revealed that the sequence of kidney ASBT cDNA gene was identical to that of human intestine ASBT gene.
结果：序列分析结果表明肾小管ASBT基因的序列与小肠ASBT序列完全一致。
3
METHODS Glioma sample and normal brain tissue of a patient were got under operation. mRNAs were extracted and reverse transcribed into cDNA.
方法取胶质瘤患者新鲜肿瘤标本及肿瘤附近正常脑组织提取mRNA，反转录成cDNA。
4
The differences of cdna ITS sequences can be used to authenticate accurately the populations of Zanthexylum bungeanum and their adulterants.
依据花椒ITS区的序列特征可以准确鉴别各居群的花椒及其混淆品；
5
The most recent studies of cdna were focused on the sequencing of new plastid genomes with comparison among relative genomes.
近几年叶绿体基因组的研究热点集中在对叶绿体基因组的测序以及亲缘关系相近物种之间的序列比对。
6
Encapsulating efficiency of cdna was determined by fluorescence spectrometer.
用荧光分光光度法测定基因包封率；
7
Cloning and Sequence Analysis of a Full-length Cysteine Proteinase cDNA in Gossypium hirsutum L.
一个陆地棉半胱氨酸蛋白酶全长cDNA的克隆及其序列特征分析。
8
Objectives: To preparing the probes of cDNA microarray in detection of the Hepatitis D virus.
前言：目的：制备诊断丁型肝炎病毒（HDV）cDNA基因芯片探针。
9
CDNA cloning and sequence analysis of coat protein genes of TMV and CMV isolated from tobacco in Yunnan province.
云南省烟草花叶病毒和黄瓜花叶病毒外壳蛋白基因克隆及序列分析。
10
Aim: To develop a PCR technique for rapid screening of recombinant plasmid in subtractive library of cDNA.
目的：消减文库构建过程中，用PCR技术快速筛选重组阳性克隆。
11
Generate sets of full-length cDNA clones and sequences that represent human genes and model organisms.
（分析出代表人类全部基因和模式生物的全长cDNA克隆和序列）。
12
Using this improved method, we analyzed the gene expression patterns of H and SP, achieving 13 differentially expressed cDNA fragments.
应用该优化的方法，比较了H和SP的基因表达图谱，分离了13个差异表达的片段。
13
Objective To clone and sequence the cDNA encoding phenylalanine ammonia-lyase (PAL) gene from Astragalus membranaceus.
目的对膜荚黄芪苯丙氨酸解氨酶基因进行克隆及序列分析。
14
Object To build up SSH cDNA libraries of down-regulated genes during odontogenic differentiation of EMCs from the first branchial arch.
目的建立第一鳃弓外胚间充质细胞牙向分化下调基因抑制消减文库。
15
We have isolated a novel immunoglobulin type cell adhesion molecule, DSCAML1, from a fetal brain cDNA library.
在胎脑文库中获得的DSCAML1属于免疫球蛋白超家族类型的细胞粘附分子。
16
Differences in gene expressions were compared by cDNA microarray in skeletal muscle of type 2 diabetic rats and normal rats.
用基因芯片技术比较2型糖尿病大鼠和正常大鼠骨骼肌基因表达谱的差异。
17
Cloning and Expression Analysis of Carboxyl-terminal Protease cDNA from Gossypium hirsutum L.
一个陆地棉羧基末端蛋白酶cDNA的克隆及其表达分析。
18
An Improved Method for Solid-phase cDNA Library Construction.
一种改进的cDNA文库固相构建法。
19
In this study, we obtained the BmDLDH cDNA sequence from NCBI and performed both bioinformatics and experiment analysis on BmDLDH gene.
本论文通过利用实验和生物信息学方法得到了家蚕二氢硫辛酰胺脱氢酶基因，并对其进行了初步分析和鉴定。
20
The lengths of the double stranded cDNA fragments were about 500 base pairs.
其双链链长，经凝胶电泳分析，约为500碱基对。
21
Objective: To explain the molecular evidence of revision of taxonomic placement of Peucedanum decursivum based on the cdna ITS sequence.
前言：目的：从核DNAITS序列角度阐明紫花前胡分类位置修订的分子基础。
22
Hence, because the gene product is easily detectable by its intense fluorescence, the gfp cDNA has become a unique reporter system.
因此，由于基因的产品很容易被其强烈的荧光探测到，绿色荧光蛋白基因，已成为一个独特的报告系统。
23
Construction of cDNA library from Sophora alopecuroides L.
苦豆子cDNA文库的构建。
24
It is more difficult to use, cdna technology when the genes have not yet been identified and several genes must be transferred.
当许多没有被鉴定的基因需要转移时，DNA技术则显得更加困难。
25
For any given redundant cDNA, this is extremely unlikely.
对于任何给定的多余的基因，这是极不可能。
26
In the forward cDNA libraries, we picked 769 positive clones randomly, which was testified by PCR analysis.
在正向文库中，随机挑取了769个阳性克隆，并进行PCR验证。
27
Construction of a Subtractive cDNA Library of the Age-related Cataract by an Improved Subtractive Hybridization and Selective PCR
用改良消减杂交结合选择性PCR法构建老年性白内障消减cDNA文库
28
Cloning of Renal Cell Carcinoma Relation Gene: Construction of a cDNA Subtractive Library of Human Renal Cell Carcinoma and Its Significance
肾癌相关基因克隆——肾癌cDNA消减文库的构建
29
A cDNA microarray study of the differential expression of genes in signal transduction pathway during hepatocarcinogenesis in tree shrews
用树鼩cDNA芯片研究树鼩肝癌中参与信号传导的部分基因变化情况
30
Cloning and Expression of a Putative Tobacco Nucleosome Assembly Protein cDNA and Purification of Its Product
烟草拟核小体组装蛋白cDNA的克隆、表达及其蛋白产物的纯化