| 1. | Both map2 and sap2 have two typical ap2 domains and a putative nuclear location signal , kksr
Map2和sap2内部都含有两个典型的ap2结构域，并且n端都具有高度保守的核定位信号。 |
| 2. | The main sequences of amino acids of hsei and hseii are same , but hseii protein has an extra 35aa in its n terminal
Hse和hse蛋白质的氨基酸序列基本相同，只是hse的n端多出35个氨基酸。 |
| 3. | The chemical degradation method established by edman in 1950 has been a routine approach for n - terminal sequencing and is widely employed by automated protein sequencer
运用edman降解进行蛋白质n端顺序测定已成为十分完善的技术，并已经实现了自动化。 |
| 4. | One n - peptide - binding scfv clone was selected from the phage antibody library using affinity panning . the target antigen , n - peptide was biotinylated using photobiotin first
N -肽是一种新发现的神经肽，其n端与阿片肽高度同源，可与阿片肽受体相互作用。 |
| 5. | Both xyna and xynb did n ' t display cellulase activity both xyna and xynb were treated by pepsin or trypsin for 30 min under 37c , their activity were n ' t decreased
胃蛋白酶、胰蛋白酶37下处理30分钟，对酶活性无影响。将纯化出的xyna及xynb进行n端序列测定。 |
| 6. | In this paper , signal peptide was added before the n - terminus of cema with the intention to reduce its toxic to plant cells while maintaining the strong antibacterial activity
本文通过在cema的n端添加信号肽，对其进行改造，以探索不降低抑菌作用的同时，降低其对植物细胞毒害作用的可能性。 |
| 7. | Spike protein was the main protective antigen inducing the neutralization antibody . the fragment containing antigenic sites b and c locating at the 5 " terminus in spike gene of tgev was deleted in prcv
Tgevs蛋白可诱导产生中和抗体，是主要的保护性抗原，其n端抗原位点b和c在prcv中缺失。 |
| 8. | This pcr product was cloned into a t - vector and resulted in a plasmid ply11 , which was used as the template to generate a rna probe of halocin c8 for screening the halc8 gene in the as7092 genome by southern blot analysis
将这段pcr产物克隆到t -载体上，形成质粒plyn ，测序结果表明pcr产物所编码的氨基酸是与halcs成熟蛋白的n端氨基酸序列是一致的。 |
| 9. | The result showed this rhbfgf had the same amino acid sequence , bioactivity and immunology characte r with nature hbfgf . the conclusion indicted the computer software - assisted analysis in genetics and molecular biology has good prospect
表达产物经sds - page电泳分析、免疫分析、活性检测，表明与hbfgf具有相同n端氨基酸序列，相同的免疫特性和生物学活性。 |
| 10. | The cdna of hn gene from b95 strain , shares a high identity between 88 % and 95 . 1 % with that of reported hn genes . the amino acid residues predicted , shares an identity between 92 . 1 % and 96 . 1 % with that of other strains
1 ，氨基酸的差异主要集中在n端18 75位。该范围内包括hn蛋白胞质区、跨膜区和细胞外区。这些变异对hn蛋白生物活性的影响还有待进一步研究。 |
