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1)  transcriptional fusion
转录融合
1.
Using promoter probe vector pCB182, three different nifH:: lacZ transcriptional fusion plasmids were constructed, (B-galactosidase activity was detected in vivo in Escherichia coli, in the presence or absence of NifA of Kleb-siella pneumoniae, respectively, the results demonstrated that; 1.
利用启动子探针质粒载体pCB182,构建了3个不同的nifH::lacZ转录融合质粒,在大肠杆菌中分别测定肺炎克氏杆菌NifA对它们的转录激活作用。
2)  CALM AF10 fusion transcript
CALMAF10融合转录
3)  fusion transcript
融合转录本
1.
However, some sporadic studies indicate that transcription can sometimes read-through the intergenic region and generates a large fusion transcript which contains the upstream gene, intergenic region and the downstream adjace.
融合转录本经基因间剪接而成为有功能的成熟转录本。
4)  fusion transcripts
融合基因转录本
1.
Methods Primers and TaqMan probes were designed for detecting various fusion transcripts,and normal ABL gene was used as the internal contro1.
方法设计TaqMan探针和引物,建立RQ-RT-PCR法对各种融合基因转录本和ABL阳性模板进行扩增,并检测177份白血病标本的转录本含量,同时做细胞遗传学检查。
5)  bcr/abl fusion transcript
bcr/abl融合转录子
1.
To investigate the biological features of leukemic cells in bcr/abl fusion transcript positive B lineage acute lymphoblastic leukemia (B ALL), 3 or 4 color flow cytometry with directly conjugated monoclonal antibodies was used to detect the immunophenotype of the cells in 26 patients with bcr/able positive B ALL and 32 patients with bcr/abl negative B ALL.
为探讨B细胞型急性淋巴细胞白血病 (B ALL)中bcr/abl融合转录子阳性白血病细胞的生物学特征 ,用流式细胞术检测 2 6例bcr/abl阳性及 32例bcr/abl阴性B ALL病例的免疫表型 ,用PCR法检测免疫球蛋白重链(IgH)基因重排。
6)  transcriptional fusion plasmid
转录融合质粒
补充资料:ρ转录终止因子
分子式:
CAS号:

性质:又称ρ转录终止因子。在转录终止时有特定效应的一种蛋白质。ρ因子能识别终止信号,防止RNA聚合酶继续抄录,并在模板上超出终点。可是,似乎有ρ-依赖的和ρ-不依赖的两者终端位点存在。

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