Background NIMS Creep Data Sheet Project, together with the preliminary studies and facilities, material selection, and testing methods, are summarized. The results of the project are described, focusing on the long-term creep strength steel and austenitic ferritic heat resistant. In some cases, the slope of the curve of stress versus time-to-rupture in the long run is different from that in the short term in a real way depending on the type of material.
Heat-to-heat variation in creep strength is recognized for ferritic and austenitic steels, even when the chemical composition of the steel examined within the range of specifications. The reason for the variation of the heat-to-heat differences in the chemical composition, the number of minor elements, and the grain size, among others. Their inherent creep strength is found in the very long term for ferritic heat resistant steel. Small number of solute elements affect the inherent creep strength, independently of strengthening precipitates or dislocation structure.
Point changes were observed in the tertiary creep stage for low alloy steels and for austenitic stainless steels when rainfall occurs during crawling. A region-splitting analysis method is proposed to evaluate the long-term creep strength of high-chromium ferritic steels. This method is used to review the allowable stress of high chromium ferritic steels in Japan. A metallographic atlas, diagram of time-temperature-precipitation, and the fracture-mode map proposed for ferritic and austenitic steels on the basis of creep-rupture specimen.
Metatranscriptomic metagenomic data analysis and complicated and usually require extensive computing resources. Utilizing a curated reference databases of genes encoded by members of the target microbiome can make this analysis more tractable. In this study, we assembled a comprehensive human vagina non-redundant gene catalog (VIRGO) which includes 0.95 million non-redundant genes. Functional gene catalog and taxonomy described. We also build vagina orthologous group (VOG) of VIRGO.
VIRGO gene-centric design and VOG provide easily accessible tools to comprehensively characterize the structure and function of the vagina and metatranscriptome metagenome datasets. To highlight the utility of VIRGO, we analyzed 1,507 metagenomes additional vagina, and identify the high level of diversity intraspesies inside and vaginal microbiota. VIRGO offers convenient reference database and toolkit that will facilitate a deeper understanding of the role of microorganisms in the vagina of women’s health and reproductive outcomes.
Catalog of NIMS creep data sheets.
Integrated Metagenome Catalog Reveals New Insights into Murine Gut Microbiome.
The complexity of the host-associated microbial ecosystems require host-specific reference catalog to survey the function and diversity of this community.
We produce a comprehensive resource, the catalog is integrated mouse gut metagenome (iMGMC), consisting of 4.6 million unique genes and 660 metagenome-assembled genome (MAGs), many (485 MAGs, 73%) of the related to the reconstruction of the full-length 16S rRNA gene sequences. iMGMC allows unprecedented coverage and resolution of the taxonomy of the intestinal microbiota of mice; ie, more than 92% of the MAGs less species-level representation in public repositories (<95% ANI matches).
Description: The T7 tag is an epitope tag composed of an 11-residue peptide encoded from the leader sequence of the T7 bacteriophage gene10. This gene encodes a T7 major capsid protein whose function is not clear.
Description: The T7 tag is an epitope tag composed of an 11-residue peptide encoded from the leader sequence of the T7 bacteriophage gene10. This gene encodes a T7 major capsid protein whose function is not clear.
Description: Goat polyclonal antibody to T7 epitope tag. T7 epitope tag is useful for the labelling and detection of proteins by immunoprecipitation, immunostaining and immunoblotting techniques. Because of its small size, it is unlikely to affect the tagged protein's biochemical properties.
Description: A monoclonal antibody for detection of T7 Tag from Null. This T7 Tag antibody is for WB. It is affinity-purified from mouse ascites by affinity-chromatography using the specific immunogenand is unconjugated. The antibody is produced in mouse by using as an immunogen synthetic peptide
Description: A monoclonal antibody for detection of T7 Tag from Null. This T7 Tag antibody is for WB. It is affinity-purified from mouse ascites by affinity-chromatography using the specific immunogenand is unconjugated. The antibody is produced in mouse by using as an immunogen synthetic peptide
Description: A monoclonal antibody for detection of T7 Tag from Null. This T7 Tag antibody is for WB. It is affinity-purified from mouse ascites by affinity-chromatography using the specific immunogenand is unconjugated. The antibody is produced in mouse by using as an immunogen synthetic peptide
Description: A monoclonal antibody for detection of T7 Tag from Null. This T7 Tag antibody is for WB. It is affinity-purified from mouse ascites by affinity-chromatography using the specific immunogen and conjugated to HRP. The antibody is produced in mouse by using as an immunogen synthetic peptide
Description: A monoclonal antibody for detection of T7 Tag from Null. This T7 Tag antibody is for WB. It is affinity-purified from mouse ascites by affinity-chromatography using the specific immunogen and conjugated to HRP. The antibody is produced in mouse by using as an immunogen synthetic peptide
Description: A monoclonal antibody for detection of T7 Tag from Null. This T7 Tag antibody is for WB. It is affinity-purified from mouse ascites by affinity-chromatography using the specific immunogen and conjugated to HRP. The antibody is produced in mouse by using as an immunogen synthetic peptide
Description: AITRL Human Recombinant produced in E.Coli is a single, non-glycosylated polypeptide chain containing 134 amino acids (81-199 a.a) and having a molecular mass of 15kDa.;AITRL is fused to a 15 amino acid T7-tag at N-terminus & purified by proprietary chromatographic techniques.
Description: A 26.5 kDa recombinant rat Clusterin with a N-terminal fusion of T7-Tag (16AA) and C-terminal fusion of His-Tag (9AA) expressed in the E.coli.
Integration MAGs, and the 16S rRNA gene of data allows a more accurate predictor of functional profile people from predictions based on 16S amplicons only. Accompanying iMGMC, we provide a set of martial arts group that represents 1,296 intestinal bacteria obtained through assembly strategies complement each other. We imagine that the integrated resources such as iMGMC, together with a collection of MAG, will increase the resolution of many future sequencing-based studies of existing and.
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