初步探讨了蛙卵中核糖核酸酶的活性组分。
Has discussed in initially the frog egg the ribonuclease active constituent.
脱氧核糖核酸酶1，牛胰腺由来，多晶体。
人的胰腺核糖核酸酶有128个氨基酸残基。
评述了近些年来抗肿瘤和抗病毒核糖核酸酶的研究进展。
In this paper, we briefly review recent advances in the research of ribonucleases pos-sessing antitumor or antiviral activities.
目的：制备并纯化抗核糖核酸酶抑制因子(RI)的抗体。
AIM: to prepare and purify the antibody against ribonuclease inhibitor (ri).
目的：探讨核糖核酸酶抑制因子对脑胶质瘤生长的抑制作用及可能机理。
Objective: to explore the role and mechanism of suppression of ribonuclease RNase inhibitor in the growth of glioma cells.
血管生成素的核糖核酸酶活性很弱，但对它的血管生成活性是至关重要的。
Although the catalytic activity of angiogenin is rather weak, it is critical for its angiogenic properties.
HBV靶向核糖核酸酶真核表达载体的构建及其在2.2.15细胞内的表达。
Construction of HBV targeted ribonuclease and its expression in 2.2.15 cell line.
本文报道了肝素、低分子肝素、透明质酸、卡介菌多糖、黄芪多糖等对核糖核酸酶的抑制作用。
It was reported that inhibition of polysaccharides including heparin lmw heparin bcg polysaccharide hyaluronic acid and astraglus polysaccharide on rnase.
目的：探讨间接酶联免疫吸附试验（ELISA）检测核糖核酸酶抑制因子（RI）在恶性肿瘤患者血清中的表达。
Objective: To detect the expression of ribonuclease inhibitor (RI) in the serum of patients with malignant tumors by indirect ELISA.
血管 生成 因子的氨基酸残基组成与核糖核酸酶具有35%的同源性，它们有着极其相似的空间结构都可以作为配体与RI结合。
There is 35% homology between the amino acid residue of the Ang and RNase and their similar spatial structure can both combine with RI as ligand.
例如，通过随机折叠，核糖核酸酶(一种小型蛋白质)的氨基酸链能形成超过1040种不同的结构，单这一种蛋白质就需要数亿年的时间来探索。
For example, by random folding, the amino-acid chain of the enzyme ribonuclease, a small protein, could adopt more than 1040 different shapes, which would take billions of years to explore.
用上述二个方法对一些蛋白如胰岛素、木瓜蛋白酶、核糖核酸酶、胰疑乳蛋白酶、胰蛋白酶、人血清白蛋白等蛋白貭的硫硫键及巯基进行测定的结果与文献上报告符合。
Results of a series of determinations of the content of disulphide bonds of a number of proteins by the above mentioned methods agreed satisfactorily with the values reported in the literature.
用上述二个方法对一些蛋白如胰岛素、木瓜蛋白酶、核糖核酸酶、胰疑乳蛋白酶、胰蛋白酶、人血清白蛋白等蛋白貭的硫硫键及巯基进行测定的结果与文献上报告符合。
Results of a series of determinations of the content of disulphide bonds of a number of proteins by the above mentioned methods agreed satisfactorily with the values reported in the literature.
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