De NovoT Cell Receptor (TCR) Sequencing Service Hybridoma Sequencing Service Services Phage Display Library Construction Phage Display Library Screening Hybridoma Services Magic™ Anti-Membrane Protein Antibody Discovery Anti-idiotype Antibody Discovery ...
因此,蛋白质序列测定有助于研究功能蛋白或活性多肽作用的机理,也为人工合成活性多肽提供了依据。蛋白de novo测序即蛋白从头测序,蛋白从头测序利用串联质谱技术对目标蛋白质进行全序列分析,不依赖已有的序列数据库,非常适合一些新发现的蛋白质或者数据库中无法匹配到的蛋白质的序列分析。
de novo protein 新的蛋白质 双语对照 例句:1.And such an inhibition might necessitate de novo protein synthesis.而这种抑制作用需要新的蛋白质合成。2.De novo synthesis of protein is essential for the complete regeneration of flagella.蛋白质重新合成对於鞭毛的再生是必须的 ...
METHODS FOR DE NOVO PROTEIN SEQUENCINGA method for determining an amino acid sequence of a polypeptide, including comprising: contacting a first sample containing the polypeptide with a first protease (e.g., Trypsin) to produce a first set of digested peptide fragments; fragmenting the first set...
Inferring the expression variability of human transposable element-derived exons by linear model analysis of deep RNA sequencing data. BMC genomics 14, 1 (2013). Article Google Scholar Nekrutenko, A. & Li, W.-H. Transposable elements are found in a large number of human protein-coding ...
With the increasing accessibility of Fourier transform (FT) mass spectrometers, top-down/middle-down MS/MS characterization of protein sequences is rapidly gaining popularity. Compared to conventional bottom-up sequencing, the top-down/middle-down approach offers the advantages of fast sample ...
We reasoned that de novo design approaches could have advantages over the traditional methods of antivenom development. First, de novo protein design does not rely on animal immunization and yields proteins that can be manufactured using recombinant DNA technology, thereby creating a source for the co...
本文主要讨论在基于物理的建模方法和人工智能的交汇处,从头蛋白质设计领域的现状,可以De novo“写入”具有新形状和分子功能的蛋白质,而无需从自然界中发现的蛋白质开始。 背景 蛋白质可以将化学反应的速度加快许多数量级,将光的能量转化为化学能,并以维持生命所需的准确性和精确度调节细胞和生物体内的无数过程。由于...
WGS sequencing on Illumina platform and de novo assembly. The sequencing libraries with insert size that peaked at 450 bp were prepared using a PCR-free protocol (Illumina Kit FC-121-3001; Illumina Inc., San Diego, CA, USA). After library profile analysis was performed by an Agilent 2100 ...
Plasmid Mini Kit I (Omega Bio-Tek) and verified by sequencing (Eurofins and Macrogen). For protein expression, competent E. coli BL21 (DE3) cells (Sigma) were transformed with the pET28*-dIG8-CC and pET28*-dIG14 plasmids and grown on LB plates supplemented with 100 µg/mL ...