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1)  Northern Light
Northern Ligh
2)  Northern blotting
Northern blot
1.
Tissue expression of the long type peptidoglycan recognition protein of mouse(mPGRP-L) was studied by RT-PCR,Northern blotting and immunohistochemistry staining.
采用RT-PCR、Northern blot以及免疫组织化学技术研究小鼠长型肽聚糖识别蛋白(mPGRP-L)在体内的表达情况。
3)  Virtual Northern blot
Virtual Northern
4)  Northern blotting
Northern印迹
1.
Methods DNA gel electrophoresis and Northern blotting hybridization were used to detect the apoptosis and the level of c myc gene,respectively.
方法 应用体外细胞培养法 ,DNA凝胶电泳技术、Northern印迹杂交技术。
5)  Northern blotting
Northern杂交
1.
The results indicated that there was distinct difference between normal stage and sterile stage of pollen in the 10 lines of maize in Northern blotting, which demonstrated thatαtubulin gene played an important role.
采用两个核背景(Mo17,77)的同核异质、同质异核细胞质雄性不育系及正常品系为材料,以合成的α 微管蛋白基因片段为探针,对玉米细胞质雄性不育系转育前后的mRNA进行Northern杂交分析,首次直接从转录水平上比较了玉米细胞质雄性不育系在败育前后α 微管蛋白基因转录量的差异。
2.
Method mRNA expressions of ARIP1,2 were analyzed by Northern blotting and their protein localizations were detected by Western blotting and immunohistochemical staining.
方法采用Northern杂交检测ARIP1,2 mRNA,Western杂交及免疫组化染色检测ARIP1,2蛋白。
3.
Northern blotting analysis reveals a 2.
Northern杂交结果显示该基因仅在脑组织中存在一个2。
6)  Northern hybridization
Northern杂交
1.
The results of Northern hybridization showed that NM23-H1B was overexpre.
采用逆转录 聚合酶链反应 (RT PCR)、Northern杂交测定NM 2 3 H1BmRNA的表达。
2.
Objective To quantify the aggrecan tnRNA expression level in tissue engineered cartilage and in vitro cultured chondrocytes by the constructed Northern hybridization probe.
32P标记aggrecan探针,Northern杂交法检测组织工程化软骨和软骨细胞中aggrecanmRNA的表达状况。
3.
The expression of endogenous rbcS and the replication of PVX-rbcS were analysed by Northern hybridization.
利用烟草叶片总RNA ,进行Northern杂交检测内源rbcS的表达和病毒复制的情况表明 ,受病毒侵染的植株内源rbcS基因的表达受到了明显的抑制 ,而病毒的复制并没有受到影响 ,重组的病毒载体上与内源基因同源的核苷酸序列诱导了内源rbcS基因的沉默。
补充资料:ligh oil
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性质:石油工业中通常指汽油、石脑油煤油和柴油。

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