1) Reverse Northern Dot Blotting
Reverse Northern杂交
2) 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。
3) 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。
4) 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
5) 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。
6) Northern blot
Northern杂交
1.
HSP72 mRNA and HSP70 expression in heart and vessel tissues of both simulated weightless and control rats exposed to heat stress (ambient temperature, Ta=43℃) and recovered at Ta of 25℃ for 1 h (CON H 1, SUS H 1) or 2 h (CON H 2, SUS H 2) were analyzed using Northern blot and Western blot.
用Northern杂交与Western印迹分析检测 4周模拟失重大鼠热应激后并在室温下恢复 1h (SUS H1)或 2h (SUS H2 )心肌、血管组织HSP70表达的变化。
2.
Northern blotting showsd that 7 of 8 clones selected randomly were specially expressed in fertile anther.
随机选取 8个克隆进行Northern杂交分析 ,结果其中 7个克隆在可育花药和不育花药之间的表达存在差异。
3.
Northern blot suggested that the transcription of Fe(II)-transporter gene was induced and strengthened by iron stress in roots; The transcription of Nramp gene was induced in both roots and leaves and strengthened in lea.
Northern杂交结果表明 ,在根中 ,irt的转录受缺铁胁迫诱导 ,并随缺铁胁迫处理天数的增加而加强 ;在根和叶中 ,Nramp基因均能得以转录且叶中的转录受缺铁胁迫诱导而加
补充资料：composite reverse osmosis membrane
分子式：
CAS号：
性质：指超薄致密皮层和支撑层材料不同的反渗透膜。其主要特点是超薄致密层薄，最薄可达30nm；膜表层形态为三维结构，有高约0.4μm，平均直径约0.07μm的突起物，使膜面积增加约一倍；超薄致密层结构的疏松和致密程度可在制膜时调节。这些特点使复合反渗透膜透水量增大，操作压力可降低至0.4～0.8MPa的超低压膜，发展了疏松超薄皮层以截留二价盐离子的纳滤膜，和脱盐率≥99.5％的致密超薄皮层的复合反渗透膜。如以聚砜膜为支撑层，芳香聚酰胺为复合皮层的FT-30膜，已经有了更疏松的NF-70膜，更致密的FT-30SW膜和表层形态不同的ESPA膜等。
CAS号：
性质：指超薄致密皮层和支撑层材料不同的反渗透膜。其主要特点是超薄致密层薄，最薄可达30nm；膜表层形态为三维结构，有高约0.4μm，平均直径约0.07μm的突起物，使膜面积增加约一倍；超薄致密层结构的疏松和致密程度可在制膜时调节。这些特点使复合反渗透膜透水量增大，操作压力可降低至0.4～0.8MPa的超低压膜，发展了疏松超薄皮层以截留二价盐离子的纳滤膜，和脱盐率≥99.5％的致密超薄皮层的复合反渗透膜。如以聚砜膜为支撑层，芳香聚酰胺为复合皮层的FT-30膜，已经有了更疏松的NF-70膜，更致密的FT-30SW膜和表层形态不同的ESPA膜等。
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参考词条