1) Northern dot Hybridization
Northern点杂交
2) Reverse Northern Dot-blotting
反向Northern斑点杂交
1.
Differential Screening Mastitis Resistant Genes of Dairy Cows by Using the Reverse Northern Dot-blotting;
奶牛乳房炎抗性基因的反向Northern斑点杂交差异筛选
3) 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 thatαtubulin 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。
4) 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。
5) Northern-blotting
Northern杂交
1.
Detection on Expressive level of pp-GalNAc-T2 in Different Tumor Cells by Northern-blotting;
Northern杂交检测多肽:N-乙酰氨基半乳糖转移酶2在不同肿瘤细胞中的表达水平
6) Northern blot hybridization
Northern杂交
1.
Total RNA was extracted at intervals,Northern blot hybridization was used to present the expression of junB mRNA,and the RNA ratio of ju.
方法 3GyX射线小鼠全身照射及不同剂量X射线照射离体脾细胞和白血病细胞 ,提取RNA ,Northern杂交 ,定量分析junBmRNA。
2.
The Northern blot hybridization results indicated that the .
根据已报道的番茄PR-NP24基因序列设计引物,经PCR克隆出长为477bp的番茄PR-NP24基因片段,以该片段制备探针,采用Northern杂交技术对该基因在番茄(WT)和乙烯反应突变体番茄(Nr,rin,T4B-11)中的表达进行了研究。
补充资料：Northern blotting
分子式：
CAS号：
性质：又称RNA印迹（法）。与DNA斑迹法过程类似的技术。用于从凝胶中转移出RNA片段转移至硝酸纤维素膜，尼龙膜等，并用探针进行杂交（称“北方”杂交）以显示目的区段的位置。显示RNA的大小及丰度。
CAS号：
性质：又称RNA印迹（法）。与DNA斑迹法过程类似的技术。用于从凝胶中转移出RNA片段转移至硝酸纤维素膜，尼龙膜等，并用探针进行杂交（称“北方”杂交）以显示目的区段的位置。显示RNA的大小及丰度。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条