结论GRA7基因在大肠埃希菌中以gst融合蛋白的形式得到表达。
Conclusion The GRA7 gene may be expressed as a GST fusion protein in E. coli.
构建含蛋白转导结构域(PTD)与脑源性神经营养因子(BDNF)融合基因的质粒，并在大肠肝菌中表达。
To construct a recombinant plasmid containing protein transduction domain (PTD) and brain derived neurotrophic factor (BDNF) fusion gene and express in e.
目的：探讨慢性粒细胞白血病（CML）患者BCR/ABL融合基因表达与中医辨证分型的关系。
Objective:To study on relationship between of BCR/ABL fusion gene expression and TCM syndrome classification in the patient of chronic myelogenous leukemia(CML).
本研究旨在探讨急性髓系白血病(aml)患者6；9染色体易位与DEK - CAN融合基因表达之间的关系及临床意义。
This study was aimed to explore the relationship of 6; 9 chromosome translocation with DEK-CAN fusion gene expression in patients with acute myeloid leukemia (AML) and its clinical significance.
结果：成功克隆了CAT的基因片段，并在大肠杆菌中得到其融合蛋白的表达。
Results: The CAT gene was cloned correctly and it's fusion protein was expressed in E.
目的：表达人免疫相关鸟苷三磷酸酶基因(IRGM) a全长融合蛋白，制备高质量的兔抗人IRGM多克隆抗体。
Aim: To express the whole length fusion protein of human IRGMa and prepare high quality rabbit anti-human immune-related gene guanosine triphosphate (IRGM) polyclonal antibody.
目的：优化融合表达抑肽酶基因工程菌的发酵条件，分离纯化抑肽酶。
Aim: to optimize the fermentation conditions of engineering bacteria expressing fusion proteins composed of aprotinin and to purify aprotinin.
这项实验发现大鼠的血液干细胞与小鼠的Purkinjie神经元相融合后，停止表达血细胞蛋白，转而表达大鼠神经元特异性基因产物。
This showed nuclei from rat blood stem cells that had fused to Purkinje cells in mice stop expressing blood cell proteins and begin to express rat neuron-specific gene products.
BCR -ABL融合基因表达出的酪氨酸激酶能引起细胞增殖、黏附和生存性质的改变，导致多种肿瘤的产生。
The tyrosine kinases expressed by BCR-ABL fusion gene can cause cell proliferation, adhesion and survival natural change, several kinds of tumors can be caused by it.
目的构建以融合蛋白形式在大肠杆菌中高效表达心钠素的重组质粒，稳定高效地获得基因工程产品心钠素。
Objective To construct recombinant plasmid with human atrial natriuretic peptide (ANP) gene in fusion form for stable and high level expression of genetic engineering product ANP in E. coli system.
研究目的：克隆表达人肠激酶轻链编码基因，以期应用于融合蛋白的切割与纯化。
Objective: To clone and express the gene of human enterokinase light chain which would be used in the cleavage and purification of fusion proteins.
目的：克隆长双歧杆菌ncc 2705株果糖结合蛋白bl 0033的基因，利用大肠杆菌表达GST -BL 0033融合蛋白并纯化。
Objective: to clone the gene of fructose binding protein BL0033 from Bifidobacterium longum NCC2705, and express and purify fusion protein GST-BL0033 in e.
将胰岛素原基因融合到金色葡萄球菌蛋白a的基因上，构建成大肠杆菌中基因融合的外分泌表达载体。
The secretion expression vector of fusion gene in E. coli has constructed by fussing the proinsulin gene to the gene of staphylococcal protein a.
结论：成功克隆葡糖基转移酶CAT基因并获得其融合蛋白的表达，为后续研究奠定了基础。
Conclusion: the target gene and its fusion protein was successfully expressed, which provide a base for the further research.
目的：研究四环素调控系统对DT390-VEGF165融合基因在人胃癌细胞中表达的影响。
Objective: To study the influence of tetracycline-controlled system on expression of the DT390-VEGF165 fusion gene in human gastric carcinoma cell.
目的构建克隆载体，分析隐匿性乙型肝炎病毒S基因的突变情况，构建其原核融合蛋白表达载体。
Objective To construct the clone vector of S gene in occult hepatitis B virus infection. To analyse its mutations and to construct its prokaryotic expression vector.
目的：在体外检测口蹄疫病毒融合表位基因的表达。
Objective: to detect the expression of the fusion epitopes gene of foot-and-mouth disease virus (FMDV) in vitro.
结论SYT SSX融合基因表达可作为诊断滑膜肉瘤新的分子诊断指标。
Conclusions SYT-SSX is a reliable index for the molecular pathological diagnosis of synovial sarcoma.
将筛选的抗体模拟肽与TSST - 1突变体基因融合或化学耦联，构建重组表达质粒。
Through crosslinking the specific peptide and the gene of TSST-1, we got the recombination plasmid.
残留白血病检测的基因标志可大致分为融合基因、变异基因和一些白血病中表达增高的基因。
Gene markers which are used to detect minimal residual disease(MRD)include fusion genes(FG), aberrant genes and some genes with high expression in leukemia disease.
本实验以轮状病毒的VP7为目的基因，构建了VP7基因的表达载体和VP7-CTB融合表达载体；
In this study, VP7 gene and CTB-VP7 fusion gene expression vectors were constructed, and a high-efficient genetic transfomation system of carrot(Daucus carota L. )
PDI与GFP融合表达研究基因的亚细胞定位，表明该基因定位在除细胞膜外的细胞质和细胞器上。
The expression of PDI-GFP fusion protein revealed its localization in both nuclear and cytoplasm compartments.
结果表明，通过与多角体基因N -端序列的融合，外源基因的表达水平得到了提高，增加的幅度为2- 3倍。
A result indicates that the expression level of a foreign gene is improved by 2 times to 3 times through fusing with the polyhedrin gene N-terminal sequence.
果与电镜和流式细胞光度计的实验结果一致，表明珠蛋白基因产物血红蛋白住杂交细胞中，能够表达并成为融合细胞的标志。
Results indicated that the resultant cybrid cells are characterized by the appearance of hemoglobin and its expression might be served as a marker for the cybrids.
果与电镜和流式细胞光度计的实验结果一致，表明珠蛋白基因产物血红蛋白住杂交细胞中，能够表达并成为融合细胞的标志。
Results indicated that the resultant cybrid cells are characterized by the appearance of hemoglobin and its expression might be served as a marker for the cybrids.
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