Quantitative RT-PCR results indicated representation of OsBTB gene expression was corresponding with the selected resistant and pathogenesis-related genes.
定量PCR结果表明该基因的表达模式与所选取的抗性及抗性相关基因的表达模式一致。
The invention relates to a method of the clinical gene chip quantitative measurement for manufacturing a standard curve, and the method belongs to the biological technology field.
本发明涉及一种可制作标准曲线的临床定量检测基因芯片方法，属于生物技术领域。
Simultaneously, the method of the invention can combine the high flux measurement and the quantitative measurement of a gene chip, and the application range of the gene chip is enlarged.
同时，本发明的方法可将基因芯片的高通量检测与定量检测结合，扩大基因芯片的应用范围。
For the first time and achieved a high sensitivity, the quantitative characteristics of the electrochemiluminescence gene detection method.
首次提出并实现了一种高灵敏度、定量的电化学发光特征基因检测方法。
There are two kinds of disease resistance, named qualitative resistance and quantitative resistance, which are controlled by single gene and multigene, respectively.
植物对病原物的抗性包括由单基因控制的质量抗病性和由多基因控制的数量抗病性两种。
Objective To explore Insulin like growth factor 1 receptor(IGF 1R)gene quantitative expression in human pancreatic cancer cells(PC 3) and the relationship of IGF 1R with apoptosis?tumorigenicity.
目的探讨胰腺癌细胞（PC-3）胰岛素样生长因子-1受体（IGF- 1R）基因的定量表达，及其与细胞凋亡、成瘤性的关系。
Quantitative RT PCR method were used to detect the mRNA levels of multidrug resistance gene in 32 leukemia children.
应用逆转录PCR结合同位素定量分析，对32例儿童白血病患者的多源耐药基因表达水平进行了研究。
Result suggested that GH gene may be a candidate gene for quantitative trait locus in pigs.
这些结果显示GH基因有可能作为数量性状基因座的侯选基因。
Results : Detection of MTHFR gene C677T polymorphism was quickly finished by realtime fluorescence quantitative RT - PCR, and the results were proved to be effective by PCR - RFLP.
结果：荧光定量方法可以快速完成MTHFR C677T基因多态性的检测，检测结果得到传统PCR-RFLP方法的证实。
Methods The expression of TUSC3 gene in 20 cases of pancreatic cancer and 6 cases of normal pancreas were detected by oligonucleotide microarray and real-time quantitative PCR.
方法利用寡核苷酸基因芯片技术和实时定量pcr技术检测20例胰腺癌组织和6例正常胰腺组织中TUSC3基因的表达。
The theories, located principle, research methods and present situation of quantitative trait loci and major gene were summarized in the paper.
本文介绍了畜禽数量性状座位及主基因的理论、定位原理、方法以及研究现状。
In recent years DD also has been adapted to quantitative environmental stimuli on bacterial gene expression.
近年来，差异显示技术也被应用于定量分析环境刺激对于细菌基因表达的影响。
The results showed that the disease resistance of F 1 hybrids was continual and had quantitative character inheritance that was controlled by multiple gene.
结果表明，不同组合后代群体的抗性呈连续性分布，表现出多基因控制的数量性状遗传特征。
QE effects were detected more often than QTL main effects, might indicate that gene expression for quantitative trait could be greatly affected by environments.
QTL与环境的互作效应比qtl的主效应更多次地被检测到，表明数量性状基因的表达显著地受到环境的调控。
Using this inducible system can be used for quantitative regulation of gene expression regulation and virulence gene function analysis and so on.
利用这种可诱导的调控系统可以用于定量调控基因表达以及进行毒性基因功能分析等方面的研究。
Methods MDR1 gene expression in case of 30 leukemia and 8 healthy persons' peripheral blood have been detested by fluorescence-quantitative reverse transcription-polymerase chain reaction (RT-PCR).
方法应用荧光定量逆转录-多聚酶链反应（RT -PCR）检测了30例急性白血病患者和8例正常人外周血MDR1基因的表达。
Results showed that 1. fluorescent quantitative RT-PCR was an efficient quantification method to detect the gene expression level and has a prospecting application in clinic;
结果显示，1．荧光定量RT干CR方法是一种定量检测基因表达丰度的有效方法，具有很好的临床应用前景；
Objective To increase the sensitivity of quantitative detection of gene transcripts in peripheral blood using real time RT PCR, two specimen processing methods were compared.
目的选择合理的标本处理方法，提高外周血基因转录本检测的灵敏度。
The gene expression of ET-1, ETAR, ETBR and ECE was evaluated by semi-quantitative reverse transcription polymerase chain response (RT-PCR).
采用半定量逆转录多聚酶链反应(RT - PCR)检测局部内皮素系统ET - 1、ETAR、ETBR及ECE的基因表达。
Fat deposition, as a quantitative trait, is regulated by multi-gene.
脂肪沉积作为一个数量性状，受多基因调控。
Fat deposition, as a quantitative trait, is regulated by multi-gene.
脂肪沉积作为一个数量性状，受多基因调控。
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