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71.
AIM: To prepare gfp-bcl-XL-contained recombinant adenovirus(rAd-gfp-bcl-XL).METHODS: Bcl-XL gene was amplified from pEGFP-C3-bcl-XL, subcloned into shuttle plasmid and formed transfer plasmid of pAdTrack-CMV-bcl-XL. Then pAdTrack-CMV-bcl-XL was linealinzed with PmeI and co-transformed into BJ5183 bacteria with adenovirus genomic plasmid of pAdEasy-1. The identified recombinant adenovirus plasmid was digested with PacI and transfected into 293 cells to package recombinant adenovirus particles. The target gene was detected by PCR.RESULTS: There were about 35% positive recombinant bacterial clones after the co-transformation of pAdTrack-CMV-bcl-XL and pAdEasy-1 into BJ5183. Recombinant adenovirus particle were produced and further amplified after the transfection of pAdEasy-1-gfp-bcl-XL into 293 cells. PCR test indicated that the recombinant Ad contained bcl-XL gene. The titer of the purified rAd-gfp-bcl-XL was 6.5×1012 PFU/L. CONCLUSIONS: The homologous recombination in bacteria is a convenient and high efficient method to prepare rAd-gfp-bcl-XL. This affords a good gene transfer vector for the gene therapy in human’s diseases. 相似文献
72.
AIM:To investigate the mechanism responsible for albumin microbubbles adherence to activated leukocytes. METHODS: In vitro studies were performed in which activated or nonactivated leukocytes were incubated with albumin microbubbles and observed under microscopy. The suspensions of leukocytes and microbubbles which contained or absented of integrins were analyzed with flow cytometry.RESULTS: A minimum of 50cells were identified under transillumination. 5 min after microbubbles were incubated with leukocytes, the number of cells interacting with microbubbles was greater for activated cells than for nonactivated cells(20.30±2.67 vs 4.50±1.43, P <0.01).Microbubbles attached to the surface of activated leukocytes were phagocytosed and remained intact for up to 30min. Microbubble attachment was inhibited notably by blocking the leukocyte β2-integrin Mac-1(P <0.01) and by VLA-4mAb slightly(P <0.05) CONCLUSION: The mechanism of albumin microbubbles attaching to and phagocytosed by leukocytes was due to β2-integrin and VLA-4 mediation. Phagocytosed microbubbles can remain at the regions of inflammation for15 min, also responsible to ultrasound. 相似文献
73.
AIM:To investigate the changes in intracellular potassium activity(aiK) and membrane potential(Vm) induced by low external sodium infusion (Low [Na]o) and to detect the mechanisms involved and the relationship between aiK and Vm. METHODS:aiK and Vm were measured in infusion with different sodium concentrations using methods of convenient and ion selective microelectrodes in guinea pig ventricular myocardium. RESULTS:Low [Na]o resulted in a decrease in aiK and an increase in Vm in a Na+ concentration-dependent manner.At the same time,contraction and resting potential increased, and action potential duration decreased markedly,but action potential amplitude was not affected. A change of the pH from 7.4 to 7.0 in low [Na]o solution reduced the decrease in aiK, but did not affect the increase in Vm.CONCLUSION:A better linear relationship appeared between the changes in aik and [Na]o or in Vm and [Na]o,while during each low [Na]o the change in both aiK or Vm may reach a new balance level. 相似文献
74.
75.
调查分析稻粒黑粉病、穗颈稻瘟等两系杂交稻制种穗期主要病害的发生原因,提出了清除菌源、轮换制种、健身栽培、对口药剂防治等防治措施。 相似文献
76.
果梅幼树对春施~(15)N-硫铵的吸收与分配 总被引:5,自引:0,他引:5
以盆栽3年生细叶青梅/毛桃为试材,研究了早春施用~(15)N-(NH_4)_2SO_4条件下,果梅对~(15)N的吸收分配规律。结果表明:由于春季土温较低,限制了植株对肥料氮的利用率。在新梢旺长期,植株从肥料氮中吸收的氮素营养主要用于新生器官的建造,且新梢成为~(15)N的主要分配中心,其次即为果实,再其次为细根。至花芽分化期,植株的生长中心已发生转移和分散,但春施氮对促进当年生枝的花芽分化和维持叶片正常光合功能仍有重要作用,此期亦是根系生长的关键时期之一,且与贮氮相比,春施氮更有利于当年新根的萌发和根系的扩大。 相似文献
77.
鸡腿蘑菌丝体的同工酶研究 总被引:7,自引:1,他引:7
用8种不同培养基配方,培养鸡腿蘑菌丝体,其同工酶分析结果表明,鸡腿蘑菌丝体酯酶(EST)同工酶谱差异明显,过氧化物酶(POD)同工酶谱差异明显。 相似文献
78.
淡紫拟青霉菌料防治大豆胞囊线虫的后效研究 总被引:6,自引:2,他引:6
淡紫拟青霉不同菌株的培养菌料,施225kg/hm2,对大豆胞囊线虫不但当年有45%~69%的较好防效,而且第2年和第3年仍然有22.5%~37.7%和7.3%~22.9%的后效,即空胞囊和被寄生的胞囊数量增加。 相似文献
79.
80.
刚察县在2001~2003年实施了“无鼠害示范区“项目,通过项目的实施天然草地的生态环境得到了明显改善,草原鼠害得到了有效控制,草地植被得到恢复,产草量明显增加,为刚察县畜牧业可持续发展打下了良好的基础. 相似文献