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- Bovine pancreatic ribonuclease A (RNase) was modified with N-hydroxysucci n imide-activated methoxypolyethylene glycol (MPEG). 采用N羥基珀酰亞胺活化酯法活化單甲氧基聚乙二醇,測定了聚乙二醇(PEG)的活化度為862%25。
- Mass spectra of proteins such as ribonuclease A(RNase A) and lysozyme were obtained with substantially enhanced abundant peaks of low charge states. 采用核糖核酸A、溶菌酶等樣品和商品化的線(xiàn)性離子阱質(zhì)譜儀對該電離源進(jìn)行了表征。
- Like RNase A, the S-protein shows the samebehavior of shifting the melting temperature of double stranded DNA although it doesnot show any ribonuclease activity. 本文報道,核糖核酸酶A經(jīng)枯草桿菌蛋白酶作用后,被切斷而形成一個(gè)20肽和s-蛋白。
- In this thesis, ribonuclease A (RNase A) was employed as a model protein to understand the formation of correct three-dimensional structure in the refolding of recombinant proteins in vitro. On this basis, the refolding mechanism in vitro was discussed. 本文以核糖核酸酶A(RNase A)為蛋白質(zhì)體外重折疊的模型蛋白,對其體外重折疊過(guò)程進(jìn)行了研究,探討了這類(lèi)目標蛋白復性過(guò)程的一些規律性的問(wèn)題。
- Human pancreatic ribonuclease has 128 amino acid residues. 人的胰腺核糖核酸酶有128個(gè)氨基酸殘基。
- This effect disappeared when EAC-I-RNA was treated with RNase. 結果表明,EAC-I-RNA能顯著(zhù)促進(jìn)淋巴細胞蛋白質(zhì)合成,此作用能被RNase所阻斷。
- The gene coding for RNase, the material is a small molecule. 這種基因能為核糖核酸酶編碼,該物質(zhì)是一種微小的分子。
- Citric acid, trisodium salt hydrate, DNAse, RNAse and Protea... 詢(xún)價(jià) 檸檬酸三鈉鹽水合物;
- The antagonism of iRNA is sensitive to RNase but not to DNase or pronase. iRNA的這兩種對抗效應均對RNase敏感而耐受DNase和Pronase。
- Once the cells are infected with HIV, RNase will hinder virus replication. 一旦細胞感染了HIV,核糖核酸酶就會(huì )阻礙病毒的復制。
- Has discussed in initially the frog egg the ribonuclease active constituent. 初步探討了蛙卵中核糖核酸酶的活性組分。
- Compressibility-structure relationships of protein: Compactness of denatured ribonuclease A. 壓力與蛋白質(zhì)結構的關(guān)系:變性核糖核酸酶A的密度。
- 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. 血管生成因子的氨基酸殘基組成與核糖核酸酶具有35%25的同源性,它們有著(zhù)極其相似的空間結構都可以作為配體與RI結合。
- Ang forms more restricted complex (Ki=7.1 X 10-16) with RI than that formed by RI and RNase A. 但Ang與RI有更大的親和力(ki=7.;1×10~(-16)M)。
- Objective:To explore the cleaved ability of RNase P target HCMV UL97 mRNA in vitro. 目的 探討核酶P對HCMVUL97mRNA的體外切割能力。
- S-protein was isolated from RNase A by polyacrylamide gel electrophoresis afterproteolytic digestion with subtilisin. 核糖核酸酶A具有DNA結合蛋白的作用。
- Seeing from the activity of DNase and RNase,they increase at the progress of consenescence in bamboo leaves. 在核酸酶的活性方面,竹葉衰老過(guò)程中,RNase與DNase的活性會(huì )增加。
- The EGS can be covalently linked to Ml RNA, the catalytic RNA subunit of RNase P, forming a new kind of ribozyme, M1GS. 將EGS共價(jià)連接到M1 RNA的3′末端成為附屬于M1 RNA的一段引導序列,稱(chēng)為GS。
- Conclusion: Rnase is rich in pancreas and small intestine and may easily denature RNA. 結論:胰腺和小腸組織RNA酶含量豐富,極易降解RNA。
- Note: If using 0.5% SDS solution to resuspend the RNA. It must be prepared in RNase free water. :如需幫助,請直接登陸子午學(xué)術(shù)論壇求助,5分鐘內解決。也可通過(guò)下列搜索尋求幫助: