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祈求

書目名稱Group A Streptococcus影響因子(影響力)




書目名稱Group A Streptococcus影響因子(影響力)學(xué)科排名




書目名稱Group A Streptococcus網(wǎng)絡(luò)公開度




書目名稱Group A Streptococcus網(wǎng)絡(luò)公開度學(xué)科排名




書目名稱Group A Streptococcus被引頻次




書目名稱Group A Streptococcus被引頻次學(xué)科排名




書目名稱Group A Streptococcus年度引用




書目名稱Group A Streptococcus年度引用學(xué)科排名




書目名稱Group A Streptococcus讀者反饋




書目名稱Group A Streptococcus讀者反饋學(xué)科排名

無底

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