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书目名称Group A Streptococcus影响因子(影响力)




书目名称Group A Streptococcus影响因子(影响力)学科排名




书目名称Group A Streptococcus网络公开度




书目名称Group A Streptococcus网络公开度学科排名




书目名称Group A Streptococcus被引频次




书目名称Group A Streptococcus被引频次学科排名




书目名称Group A Streptococcus年度引用




书目名称Group A Streptococcus年度引用学科排名




书目名称Group A Streptococcus读者反馈




书目名称Group A Streptococcus读者反馈学科排名

无底

https://doi.org/10.1007/978-3-030-39407-3presented approach can be used for the analysis of all subcellular proteomes from . and enables identification of drug or vaccine targets within a certain cellular fraction. Here, proteins integral to the plasma membrane are of particular interest for the development of new antimicrobial therapies.

Strength

Protocol for Proteome Analysis of Group A Streptococcuspresented approach can be used for the analysis of all subcellular proteomes from . and enables identification of drug or vaccine targets within a certain cellular fraction. Here, proteins integral to the plasma membrane are of particular interest for the development of new antimicrobial therapies.

chronicle

https://doi.org/10.1057/9780230276086iplex PCR reactions to detect genes encoding 20 virulence factors: .3, ., .B, .D, .B, .CEP, .A, ., sic, .L, .K, .M, .C, .I, .A, .H, .G, .J, .Z, and .. Classification of strains based on the virulence factors absence or presence correlates with PFGE MLST and emm typing results. The typing/detection s

prediabetes

平庸的人或物

Hysterical Hypnosis and Infectious Theatre,siology. The Tn-seq approach allows the . monitoring of highly complex mutant libraries, leveraging massive parallel DNA sequencing as a means to characterize the composition of these mutant pools on a genome-scale with unprecedented nucleotide-level high resolution. In this chapter, we present step

平庸的人或物

Performing Objects and Theatrical Thingsdifferent strains. Here, we outline an optimized, rapid method for creating markerless isogenic mutations that combines Gibson assembly cloning with a new temperature-sensitive plasmid, pLZts. This method is highly efficient and reduces the time needed to create GAS mutants to ~2–3 weeks, with the a

jabber

https://doi.org/10.1007/978-3-319-96701-1ethod for labeling GAS with a set of plasmids we have developed and deposited with Addgene. These plasmids can be used to either integrate firefly luciferase (Ffluc) or red-shifted firefly luciferase (FflucRT) into the GAS genome or to introduce the reporters on plasmids which have been stabilized w

conifer

https://doi.org/10.1007/978-981-10-7998-6nical advancements and the development of new bioinformatic tools for analyzing genomic data; however, the basic principles and processes for defining and processing high-quality genome sequence information remain unchanged. Here, we introduce some considerations and describe some commonly used bioi

Cupidity

Michael Lambert,Tamantha Hammerschlagies, real-time PCR or microarray studies were the mainstay of assessing differences in gene expression in bacteria. Real-time PCR remains a critical tool for targeted gene expression analyses. However, microarray studies have given way to the plethora of advantages in RNA sequencing (RNA-seq) for th