Influence of Mycobacterium tuberculosis 19 kDa lipoprotein upon the expression and distribution of Toll-like receptor-2 on the surface of macrophages 结核分枝杆菌P19对巨噬细胞TLR-2表达及分布的影响
Characterization of 36 kDa Outer Membrane Proteins of Six Pathogenic Vibrio Species 6种海洋致病性弧菌36kDa外膜蛋白特性分析
Document classification algorithm based on KDA and SVM 基于KDA和SVM的文档分类算法
Welcoming Address by an Official of the MOE 211 Project Office on the 211 Project KDA Exhibition 教育部“211工程”办公室负责人就“211工程”重点学科成就展致欢迎辞
Preliminarily establishing dipstick fast diagnostic system using soluble egg antigen ( SEA) 38 kDa molecule of Schistosoma japonicum 日本血吸虫可溶性虫卵抗原38kDa分子Dipstick快速诊断模式的初步建立
Based on the idea of subspace projection, an optimal kernel discriminant analysis ( OKDA) is given and used to extract features from a range profile. 核判别分析(KDA)是一种抽取非线性特征的有效方法,但它会因为奇异性问题而难以求解。
Ear Recognition Using KDA/ GSVD and SVM 基于KDA/GSVD和支持向量机的人耳识别
Kernel discriminant analysis ( KDA) is an effective method for nonlinear feature extraction in radar target recognition, but it is usually difficult to solve due to the singular problem. 特征提取是雷达目标识别研究中的重要问题,有效、稳健的特征是提高识别率的关键。
ChAT, a large molecule with a molecular weight of 69 kDa, cannot pass through the biological membrane. 然而,ChAT是一分子量69kDa的蛋白质,难以通过血脑屏障和细胞膜。
A Novel Face Features Extraction Method Based on DCT and KDA 基于DCT和KDA的人脸特征提取新方法
Methods: With recombinant 38-KDa antigen of M. tuberculosis coating soid carrier. 方法:采用结核分枝杆菌38&KDa基因重组抗原包被固相载体进行酶联免疫测定。
Sixty kDa molecules had a high VE solubilizing activity and proteolytic activity. 60kDa分子具有很强的卵黄膜溶解活性和蛋白酶活性。
Putative protein molecular weight was 113.7 kDa with an isoelectric point of 7.88 and no predicted transmembrane domain. 推测的蛋白质分子量为113.7kDa,等电点为7.88,蛋白质预测无跨膜区。
Its subunit molecular weight was 66 kDa measured by SDS-PAGE. 用SDS-PAGE测得亚基相对分子质量为66kDa。
Like Yunnan isolate, female worms of Guangxi isolate also showed marked 84 kDa bands. 广西的日本血吸虫与云南的虫体一样,雌虫在84kDa处亦呈现明显的条带。
The purification technology and parameters for 32 kDa were researched with ion exchange chromatography and gel chromatography, detected with SDS-PAGE. 采用离子交换层析、凝胶层析,以SDS-PAGE检测,对其中一个蛋白进行了分离纯化研究,得到了32kDa蛋白的纯化工艺和参数。
SDS-PAGE analysis showed that the molecular mass of recombinant APX was about 29 KDa. SDS-PAGE分析显示,重组蛋白大小约为29KDa。
SDS-PAGE analysis indicated that the about 18 kDa molecule can bind to the yeast cells. SDS-PAGE分析结果表明,一种分子量约为18kDa的分子可以结合到热致死酵母细胞上,增强吞噬作用。
Molecular weight were measured as 41.83 kDa by SDS-PAGE. SDS-PAGE测得分子量为41.83kDa。