大多数分子标记体系的利用都取决于聚合酶链反应（PCR），这是一项扩增特定DNA序列的重要技术。
Use of most molecular marker systems depends on the polymerase chain reaction (PCR), which is an important technique for amplifying specific DNA sequences.
这个文件还包含了有关出现电源故障时执行的操作(如果系统支持)、以及在检测到Ctrl - Alt - delete键序列时应该如何反应的信息。
This file also contains information about what to do when a power failure occurs (if the system supports it) and how to react when it detects the Ctrl-Alt-Delete key sequence.
虽然这种技术在某些类型细胞上的应用十分奏效，但是它现在主要被用于探测重复DNA序列，而且需要使用连续的反应。
Although this technique has proven its efficiency on several types of cells, its current utilization is limited to the detection of repeated DNA sequences and requires the use of sequential reactions.
应用聚合酶链反应得到2株蓝绿藻的毒素聚酮合成酶(PKS)基因，并进行基因序列分析。
Gene of polyketide synthase (PKS) from 2 toxin-producing cyanobacteria was prepared by polymerase chain reaction and the gene sequence was analyzed.
方法运用序列特异性引物聚合酶链反应技术，检测无亲缘关系湖北汉族健康人136例、食管癌组42例患者的HLA-DQB1等位基因。
METHODS HLA-DQB1 gene polymorphisms were typed by sequence specific primer based polymerase chain reaction, in 42 patients with esophageal neoplasm and 136 normal control subjects.
马传染性贫血病毒是反转录病毒科慢病毒属的成员之一，不仅与人免疫缺陷病毒具有序列同源性，而且与其血清具有交叉反应。
Equine infectious anemia virus (EIAV) is a lentivirus. It related in sequence to the human immunodeficiency virus (HIV) and reacted with acquired immunodeficiency syndrome (AIDS) patient sera.
本发明一般性涉及编码与非生物胁迫反应相关蛋白质的核酸序列和植物的非生物胁迫耐性。
This invention relates generally to nucleic acid sequences encoding proteins that are associated with abiotic stress responses and abiotic stress tolerance in plants.
已经采取突变研究来定位该亚单位的反应中心而且该研究提供了能够解释在基因功能方面的序列差别的背景知识。
Mutational studies have been used to map the reaction centres of this subunit and these provide a background which enables interpretation of sequence differences in terms of gene function.
采用逆转录聚合酶链反应(RT - PCR)扩增汉坦病毒基因组M片段G1区基因序列并测序。
G1 gene sequence of m fragment from hantavirus genome was amplified by reverse transcription polymerase chain reaction (RT-PCR) and analyzed.
将位于多巴胺运输器基因3'端未转译区段的40 -碱基多形性重复序列予以纯化、经聚合酶链锁反应放大。
A 40-base polymorphic repeat sequence located in the 3 '-untranslated region of the DAT gene was purified and amplified by polymerase chain reaction (PCR).
实证表明，中国证券市场的反向利润绝大多数源于股票的反应过度，有少部分源自共同因素在时间序列上的负相关。
Empirical evidence shows that the majority of contrarian profits in Chinese stock market are due to overreaction while a small part is due to negative correlation of common factor in time series.
它们是由很多人工合成、计算机生成的蛋白序列组成，可以促使免疫系统对不同的病毒菌株作出反应。
They are composed of many sets of synthetic, computer-generated sequences of proteins that can prompt the immune system to respond to a variety of strains.
并把分型结果与采用聚合酶链反应-序列特异性引物（PCR-SSP）获得的结果进行比较。
The results of genotyping were compared with those obtained with the polymerase chain reaction method using sequence specific primers ( PCR-SSP).
方法利用聚合酶链反应-序列特异引物(PCR -ssp)法，对189例银屑病患者和273例健康人的HLA - DQA1和DQB1等位基因进行检测。
Method Polymerase chain reaction sequence specific primers (PCR-SSP) method was used to analyze the frequencies of HLA-DQA1 and DQB1 alleles among 189 patients with PV and 273 healthy controls.
由于序列相似性，该抗体可能与CDK2和CDK3发生交叉反应。
Based on sequence similarity, the antibody may cross-react with CDK2 and CDK3.
DNA模板指导的有机合成反应具有序列特异性特点。
DNA template directs organic synthesis by sequence-specificity recruiting reactants linked to complementary DNA.
生长素早期或原初的反应基因的启动子通常包括最小的生长素反应元件TGTCTC序列。
The promoters of auxin early or primitive reaction gene generally include the minimal auxin reaction element sequence (TGTCTC).
方法利用聚合酶链反应（PCR）产物直接测序，对10例血液标本进行了HLA-DPB1、DRB外显子2的序列分析，并将测定结果与基因型核酸序列数据库进行比较。
Methods Sequences of HLA-DPB1, DRB exon2 of 10 samples were analysed by direct sequencing of PCR products. The results of sequencing were compared with their corresponding sequence data.
采用厌氧序列间歇反应器与好氧序列间歇反应器相结合的技术，处理生物制药废水。
The technology combined anaerobic sequencing batch reactors with aerobic sequencing batch reactors was used to treat biochemical medicine wastewater.
在这项任务中，参加者需要了解一套刺激反应序列，并提供一个单一的代表数值答案。
In this task, participants are required to understand a set of stimulus-response sequences and supply a single representative numerical answer.
对导致反应堆控制系统故障的事故序列进行了识别，计算了该系统顶事件的概率。
The event sequences leading to the reactor control system failure are identified and the top event probability of this system is calculated.
阳性培养物用生化反应、协同凝集试验、代谢抑制试验、聚合酶链反应和DNA序列测定等方法进行鉴定。
Biochemical reaction, coagglutination test, metabolism inhibition test, polymerase chain reaction (PCR) assay, and DNA sequencing were employed to identify the isolated microorganisms.
BLAST分析表明，其中19个EST序列与已知功能基因序列同源性很高，分别参与了植物的防卫反应、胁迫反应、细胞解毒和信号转导等。
BLAST analysis revealed that 19 ESTs had high homology with known genes in GenBank involved in defense response, stress reaction, disease defense detoxification and signal transduction.
处于这序列的人群，会激发不同的个人、家庭、社会、国家以及国际的种种反应。
Where a population lies on the continuum can be thought to evoke different individual, household, community, national, and international responses.
方法：采用序列特异性引物聚合酶链反应的方法对汉族72例uc患者和314例正常对照者HLA - DRB1基因分型。
Methods: By using polymerase chain reaction-sequence specific primers, frequency of HLADRB1 alleles in 72 patients with UC and 314 healthy controls were detected.
分别设计MSX1、PAX9基因特异性引物，聚合酶链反应扩增全部外显子编码区和内含子-外显子剪接序列，产物纯化后直接测序。
Specific primers were designed for MSX1 and PAX9 respectively. Mutation analysis was performed by direct sequencing of all the coding exons and intron-exon boundaries.
方法运用聚合酶链反应-序列特异性引物（PCR-SSP）法，对38例山东汉族人GPP与94例健康对照进行HLA-DQB1等位基因分型。
Methods The distributing frequencies of HLA-DQB1 alleles were detected with polymerase chain reaction-sequence specific primers (PCR-SSP) in 38 GPP patients and 94 healthy subjects from Shandong.
根据肺炎支原体细胞粘附素蛋白质的基因保守区两侧序列，设计并合成一对变性寡核苷酸引物L2R2，用于以鸡毒支原体S6株基因组DNA为模板的PCR反应。
A pair of degenerate oligonucleotide primers named L2R2were synthesized according to conserved regions of the cytadhesin proteins from M. pneumonias. MG-S6DNA were used as model in L2R2 primered PCR.
根据肺炎支原体细胞粘附素蛋白质的基因保守区两侧序列，设计并合成一对变性寡核苷酸引物L2R2，用于以鸡毒支原体S6株基因组DNA为模板的PCR反应。
A pair of degenerate oligonucleotide primers named L2R2were synthesized according to conserved regions of the cytadhesin proteins from M. pneumonias. MG-S6DNA were used as model in L2R2 primered PCR.
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